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81.
Tabatabaei A. Fotowat A. Delurio M. Navid S. 《Solid-State Circuits, IEEE Journal of》1998,33(1):156-163
A buffer that can source or sink up to 10 mA with a slew rate of 130 V/μs in a series RC load of 500 Ω and 12 nF is introduced. The buffer has a standby current of 400 μA which is reduced to 50 nA in less than 100 ns in power-down mode. It operates with a 2.7-V supply and is designed for personal communications applications such as Digital Enhanced Cordless Telecommunications (DECT). The adaptive biasing technique employed in this design makes it suitable for other applications like high-speed sample-and-hold or transconductance stages 相似文献
82.
Behbahani F. Fotowat A. Navid S. Gaethke R. Delurio M. 《Solid-State Circuits, IEEE Journal of》1997,32(9):1446-1450
This paper describes the implementation of a low distortion mixer for direct up-conversion and high IF systems. A Gilbert cell with a low distortion transconductance constitutes the mixer core. A current feedback loop is used to linearize the transconductance stage, achieving an alternate channel leakage of -71 dBc with a power penalty of 15%. The mixer operates from 2.7 to 7.5 V of supply voltage and over a temperature range of -40 to 85°C. It provides -3 dBm output power while drawing 7.5 mW from a 3-V supply. The mixer is implemented in 1-μm BiCMOS for a global system for mobile communications (GSM) chip set 相似文献
83.
The ternary antimonides ZrSi(delta)Sb(2-delta), HfGe(delta)Sb(2-delta), and ZrGe(delta)Sb(2-delta) were prepared by annealing of the elements in stoichiometric ratios below 800 degrees C. ZrSi(delta)Sb(2-delta) was earlier erroneously described as the binary "beta-ZrSb(2)", which does not exist as such, because the incorporation of tetrel atoms is necessary for the formation of this structure. ZrSi(delta)Sb(2-delta) has a small yet significant phase width with at least 0.066(7) < or = delta < or = 0.115(3), whereas the Ge analogues exist with larger tetrel concentration, i.e., ZrGe(0.211(5))Sb(1.789) and HfGe(0.205(6))Sb(1.795). The whole series of title compounds crystallizes in the Co(2)Si type (space group Pnma), with lattice dimensions of, e.g., for ZrGe(0.211(5))Sb(1.789), a = 730.4(1) pm, b = 395.13(6) pm, c = 957.6(2) pm, V = 0.27635(7) nm(3), Z = 4. The anionic substructure comprises infinite ribbons formed by the atom sites Q1 and Sb2, with Q1 being mixed occupied by Si or Ge and Sb atoms. These ribbons exhibit Q1-Q1 single bonds and Q1-Sb2 "half" bonds. Assuming the validity of the 8 - N rule, one can assign seven valence-electrons to Sb2 but only five to Q1, which might explain the preference of the tetrel atoms for the latter site. 相似文献
84.
David Boldrin Freya Johnson Ryan Thompson Andrei P. Mihai Bin Zou Jan Zemen Jack Griffiths Patrik Gubeljak Kristian L. Ormandy Pascal Manuel Dmitry D. Khalyavin Bachir Ouladdiaf Navid Qureshi Peter Petrov Will Branford Lesley F. Cohen 《Advanced functional materials》2019,29(40)
Multicomponent magnetic phase diagrams are a key property of functional materials for a variety of uses, such as manipulation of magnetization for energy efficient memory, data storage, and cooling applications. Strong spin‐lattice coupling extends this functionality further by allowing electric‐field‐control of magnetization via strain coupling with a piezoelectric. Here this work explores the magnetic phase diagram of piezomagnetic Mn3NiN thin films, with a frustrated noncollinear antiferromagnetic (AFM) structure, as a function of the growth induced biaxial strain. Under compressive strain, the films support a canted AFM state with large coercivity of the transverse anomalous Hall resistivity, ρxy, at low temperature, that transforms at a well‐defined Néel transition temperature (TN) into a soft ferrimagnetic‐like (FIM) state at high temperatures. In stark contrast, under tensile strain, the low temperature canted AFM phase transitions to a state where ρxy is an order of magnitude smaller and therefore consistent with a low magnetization phase. Neutron scattering confirms that the high temperature FIM‐like phase of compressively strained films is magnetically ordered and the transition at TN is first‐order. The results open the field toward future exploration of electric‐field‐driven piezospintronic and thin film caloric cooling applications in both Mn3NiN itself and the broader Mn3AN family. 相似文献
85.
86.
Polymerization of ethylene using a series of binuclear and a mononuclear Ni (II)‐based catalysts
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Mostafa Khoshsefat Gholam Hossein Zohuri Navid Ramezanian Saeid Ahmadjo Meisam Haghpanah 《Journal of polymer science. Part A, Polymer chemistry》2016,54(18):3000-3011
A novel series of homo‐, bi‐, and mononuclear Ni(II)‐based catalysts (BNCn n = 1–4, MNC4) were used for ethylene polymerization. The optimum conditions for the catalyst BNC4 (the highest catalytic activity) was obtained at [Al]/[Ni]=2000/1, Tp = 42 °C, and tp = 20 min that was 1073 g PE/mmol Ni h. In theoretical study, steric and electronic effects of substituents and diimine backbone led to prominent influence on the catalyst behavior. The highest MV was resulted from polymerization using BNC4; however, the highest unsaturation content was obtained from BNC1. GPC analysis showed a broad MWD (PDI = 17.8). BNC1 and BNC2 in similar structures showed broad peaks in DSC thermogram, while BNC3 and BNC4 with more electronic effects showed a peak along with a wide shoulder. Monomer pressure increasing showed enhancing in activity of the BNC4, meanwhile a peak with shoulder to a single peak in DSC thermogram and uniformity in morphology of the resulted polymer were observed. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3000–3011 相似文献
87.
Irannejad-Gheshlaghchaei Navid Zare Abdolkarim Sajadikhah Seyed Sajad Banaei Alireza 《Research on Chemical Intermediates》2018,44(10):6253-6266
Research on Chemical Intermediates - A novel dicationic ionic liquid, N,N,N′,N′-tetramethyl-N,N′-bis(sulfo)ethane-1,2-diaminium mesylate [TMBSED][OMs]2), has been produced, and... 相似文献
88.
Navid Sharifi 《Heat and Mass Transfer》2013,49(10):1489-1501
Thermal vapor compressor (TVC) is a device for compressing vapor in water–steam cycles and frequently used in desalination systems. Large amounts of useless vapor can be compressed by this device and the efficiency of a desalination unit is effectively enhanced through this process. Motive steam is injected into the TVC through a convergent–divergent nozzle and accelerated to supersonic velocities. The low pressure steam is entrained at the upstream zone and mixed with this highly compressible motive flow within the TVC. In the current study, the flow field of an experimental TVC is scrutinized in both axisymmetric and three-dimensional approaches and compared with experimental measurements. Since the steam collector at the suction surface of the TVC has a curved shape and may undermine the symmetry of the flow on either side of the central axis, the second objective of this study is to reveal the deviation of the symmetric assumption from the real non-symmetric condition of entering steam flow into the TVC. Results show that the presence of a bending at the inlet side has approximately negligible effects on the mixing phenomenon and the flow remains symmetric around the central axis. Hence, there is no need to consider the collector geometry in further simulations and the performance parameters of the TVC would be sufficiently obtained through an axisymmetric method with a substantial reduction in the computational cost and time. 相似文献
89.
A study of the mechanism of the catalytic transformation of mixed ethyl acetate (EA) + methyl acetate (MA) (50:50 v/v) to hydrocarbons over HZSM‐5 (Si/Al ratio of 9) catalyst was conducted. The reaction was carried out in a continuous fixed‐bed reactor under atmospheric pressure and in the temperature range 250–390°C and with weight hourly space velocity of 3.2 and 4.6 h?1. The distribution of products including monoaromatics, fused ring aromatics and oxygenates was determined using GC‐MS. The product distribution was controlled by temperature. The oxygenate components (kinetically controlled products) were transformed into aromatics (thermodynamically controlled products) with an increase in temperature. The effluents were benzene‐free or with low content of benzene and toluene. Two intermediates were proposed for this conversion to hydrocarbons over HZSM‐5: cyclobutane‐1,3‐dione and/or acetic acid (AA) as ketene source. Furthermore, AA and mesityl oxide (MO) were selected as potential intermediates in the transformation of mixed EA + MA into hydrocarbons over HZSM‐5. It is suggested that ketene dimerization, the phenolic pool and the condensation reaction between ketene and MO are the probable mechanism routes for AA conversion. Aldol condensation, Michael addition, cracking, isomerization and ketene formation are the presumable pathways for MO conversion over HZSM‐5. 相似文献
90.
Mohammad Navid Soltani Rad Ali Khalafi‐Nezhad Somayeh Behrouz 《Helvetica chimica acta》2009,92(9):1760-1774
The syntheses of some novel carboacyclic nucleosides, 17a – 17o , containing oxiconazole‐like scaffolds, are described (Schemes 1–3). In this series of carboacyclic nucleosides, pyrimidine as well as purine and other imidazole derivatives were employed as an imidazole successor in oxiconazole. These compounds could be prepared in good yields by using two different strategies (Schemes 1 and 2). Due to Scheme 1, the N‐coupling of nucleobases with 2‐bromoacetophenones was attained for 18a – 18e , and their subsequent oximation affording 19a – 19e and finally O‐alkylation with diverse alkylating sources resulted in the products 17a – 17g, 17n , and 17o . In Scheme 2, use of 2‐bromoacetophenone oximes 20 , followed by N‐coupling of nucleobases, provided 19f – 19j whose final O‐alkylation produced 17h – 17m (Scheme 2). For the rational interpretation of the dominant formation of (E)‐oxime ethers rather than (Z)‐oxime isomers, PM3 semiempirical quantum‐mechanic calculations were discussed and the calculations indicated a lower heat of formation for (E)‐isomers. 相似文献