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1.
A cold cathode discharge tube has an auxiliary tube attached from which cathode-rays are projected against the main cathode. A photo-electric cell, attached to a monochromatic illuminator, is used to measure relative intensity distribution of Hγ and Hδ respectively, from the main cathode through the cathode dark space into the negative glow with and without excitation of the auxiliary tube. When the main cathode is bombarded by the electron stream the intensity of spectral illumination in the negative glow is increased by about 20 per cent. This increase does not result from the mere addition of an illumination, which appears when the auxiliary tube is alone excited, to the illumination of the main discharge, but may be attributed to the production of soft X-rays in the gas which are capable of exciting the gas molecules.R. Seeliger and co-workers have investigated spectrophotometrically the several characteristic sections of a cold cathode discharge tube. Their method consisted of an examination, with a microphotometer, of spectrograms taken at points along the discharge. The intensity distribution of any spectral line was found continuous in passing from one portion of the discharge to another, e.g., from the Faraday dark space into the positive column, and that the maxima of illumination for different lines appeared displaced relative to one another.A. Wehnelt and A. Jachan demonstrated with several experimental arrangements the effect of bombarding the cold cathode of an ordinary discharge tube with a beam of cathode-rays. There resulted an increase in the total intensity of illumination in the tube together with a shrinkage of the cathode dark space.The purpose of the present investigation was to examine the effect such an electronic bombardment would produce upon the spectral intensity distribution near the cathode of a hydrogen discharge in and alone were capable of investigation.  相似文献   

2.
This paper outlines the cathode characteristics of thoria which lead to its selection in certain cases where the barium-strontium oxide cathode is unsuitable. Dependable values of pulsed thermionic emission of 4 amps/cm.2 at 1600° C. and 14 or 15 amps/cm.2 at 1800° C. are available.The decay of emission with time is much less rapid than with barium-strontium oxides, the time constants being of the order of one-tenth of 1 second. Maximum d-c. emission, that is, equilibrium emission after decay, is found to be between 1 and 5 amps/cm.2. Although when compared to barium-strontium oxide the activation phenomena are not prominent, it is found that the same essential pattern exists. For use in pulsed applications the life of a thoria coated cathode is determined by its evaporation rate. At 1800° C. where 14 amps/cm.2 is available the coating disappears at the rate of 1 mil thickness in about 300 hours.  相似文献   

3.
The rate of evaporation of electrons, νe, from a thoriated tungsten filament depends on the temperature T and on θ, the fraction of the surface covered by thorium atoms. The relation of νe to θ and T has been given by Brattain and Becker. From νe the change in contact potential V of the filament surface produced by the adsorbed thorium can be calculated by the Boltzmann equation. Knowing σ the number of thorium atoms per cm.3, the dipole moment M of each is given by V = 2τσM. By an equation already used for Cs films on tungsten, the 2-dimensional equation of state of the adsorbed film can be calculated from M. Then by Gibbs' adsorption equation the relation of the atom evaporation rate νa to θ and T can be determined. It is thus calculated that in the range from θ = 0.2 to θ = 0.6, νa varies in proportion to ? where H = 8.1 in good agreement with the value H = 7.8 given by Brattain and Becker's measurements. A recalculation of the data of numerous experiments in 1921–1923, using the new relations of νe to θ1 gives data on νa as a function of T and θ in good agreement with the values of νa calculated from νe.The diffusion coefficients of Th through tungsten crystals, along grain boundaries and over the free filament surface, are calculated. A theory is given for the cause of the variation in the surface diffusion coefficient with σ. The probable mechanism of the production of the metallic thorium within the filament is discussed. At 2400° the thorium which arrives at the surface along grain boundaries, for some unknown reason, does not spread out over the surface as it does at lower temperatures (1900–2100°).  相似文献   

4.
BackgroundCyclodextrin glucanotransferase (CGTase) from Amphibacillus sp. NPST-10 was covalently immobilized onto amino-functionalized magnetic double mesoporous core–shell silica nanospheres (mag@d-SiO2@m-SiO2-NH2), and the properties of the immobilized enzyme were investigated. The synthesis process of the nanospheres included preparing core magnetic magnetite (Fe3O4) nanoparticles, coating the Fe3O4 with a dense silica layer, followed by further coating with functionalized or non-functionalized mesoporous silica shell. The structure of the synthesized nanospheres was characterized using TEM, XRD, and FT-IR analyses. CGTase was immobilized onto the functionalized and non-functionalized nanospheres by covalent attachment and physical adsorption.ResultsThe results indicated that the enzyme immobilization by covalent attachment onto the activated mag@d-SiO2@m-SiO2-NH2, prepared using anionic surfactant, showed highest immobilization yield (98.1%), loading efficiency (96.2%), and loading capacity 58 µg protein [CGTase]/mg [nanoparticles]) which were among the highest yields reported so far for CGTase. Compared with the free enzyme, the immobilized CGTase demonstrated a shift in the optimal temperature from 50°C to 50–55°C, and showed a significant enhancement in the enzyme thermal stability. The optimum pH values for the activity of the free and immobilized CGTase were pH 8 and pH 8.5, respectively, and there was a significant improvement in pH stability of the immobilized enzyme. Moreover, the immobilized CGTase exhibited good operational stability, retaining 56% of the initial activity after reutilizations of ten successive cycles.ConclusionThe enhancement of CGTase properties upon immobilization suggested that the applied nano-structured carriers and immobilization protocol are promising approach for industrial bioprocess for production of cyclodextrins using immobilized CGTase.  相似文献   

5.
It has been shown that electrons with 11.5 volts energy can dissociate a hydrogen molecule into its two constituent atoms, but up until recently no experiments have been performed to see whether fast positive ions are able to dissociate hydrogen.In the present experiments Li or Cs positive ions of various velocities are produced in a tube containing hydrogen molecules. The tube is immersed in liquid air, and the rate of decrease of pressure of hydrogen is measured as a function of the velocity of the positive ions. It is found that with no positive ions entering the tube there is a certain decrease in the pressure of the hydrogen due to its thermal dissociation on the hot filament and its subsequent condensation on the cold walls of the tube. With ions of energies from 15 to 320 volts flowing in the tube the rate of decrease of pressure is greater, showing a formation of some condensible product due to the action of the ions.The rate of pressure decrease with the voltage applied has been found to be proportional to the ion current flowing. The rate per unit current is proportional to the pressure; and the rate per unit current per unit pressure is practically independent of the voltage for Li and Cs ions of energies from 15 to 320 volts.The effect has been shown not to be due to secondary electrons.The process may be due to the formation of alkali hydrides in the gas phase. The number of hydrogen molecules disappearing per positive ion entering the tube varies from 0.01 to 0.5. No critical potentials have been found in this experiment, in disagreement with recent experiments of Leipunsky and Schechter.  相似文献   

6.
Using the velocity analyzer of Zartman with improved technique the combined velocity spectrum of Bi atoms and Bi2 molecules was obtained at 827°, 851°, 875°, 899°, 922°, 947° C. From the spectral distribution curves the relative abundance of Bi atoms and Bi2 molecules in the beams at the above temperatures could be determined to 1 per cent. The vapor pressure curve of Bi was obtained experimentally by the method of effusion and the values so obtained were combined with the degree of dissociation of the vapor as computed from the beams to give the heat of dissociation. The heat of dissociation was computed from the data, assuming the pressure to be given by the temperature of the crucible Tc. In calculating the heat of dissociation, the equilibrium temperature was taken as that of the slit chamber Ts which was 24° above Tc. The results of these calculations plotted with log10Kp as ordinates against 1Ts give a straight line whose slope yields the value of the heat of dissociation as 77,100±1200 calories. The curves for the distribution of velocities observed and computed on the assumption of a given ratio of Bi atoms to Bi2 molecules in the beam were compared in an attempt to test the law of distribution of velocities. On the high velocity side agreement in two curves was obtained within the limits of experimental accuracy. On the low velocity side important deviations were noted of such a sort that the observed curves below a velocity α2, (α is the most probable velocity) gave more molecules than the theory demanded. Other deviations were observed on some of the runs taken with a fourth slit in which a deficiency of molecules was observed between velocities of .75α and α2. This deviation was probably due to a warping of the fourth slit carriage due to heat. The nature of the variation at velocities less than α2 indicated the presence of molecules of greater mass than Bi2 in the beam and at the lower temperatures a distinct peak corresponding to Bi8 molecules was observed which were present to less than 2 per cent. The vapor pressure curve for Bi was determined by least square reduction of the observed points to be given by log10 P = ? 52.23 × 195.26T + 8.56 between 1100° and 1220° abs. It lies very close to the extrapolated curve given in the International Critical Tables.  相似文献   

7.
This paper is concerned with the problem of discrete-time event-triggered H control for networked cascade control systems (NCCSs) with time-varying network-induced delay. First of all, an event-triggered scheme is introduced to this system for reducing the unnecessary waste of limited network bandwidth resources. Considering the effect of time-varying delay, a new mathematical model for this system is constructed. In this paper, based on the model and Lyapunov functional method, the co-design method of event-triggered parameter, state feedback primary controller and secondary controller with H performance is derived via linear matrix inequality technique. To illustrate the effectiveness of the proposed method, a simulation example considering a main steam temperature cascade control system is given. The proposed method emphasizes the application in the corresponding industrial control systems, it can be found that this method is superior to the one in some existing references, and the provided example demonstrates the effectiveness of the co-design method in the networked cascade control systems with event-triggered scheme.  相似文献   

8.
Mechanically exfoliated two-dimensional ferromagnetic materials (2D FMs) possess long-range ferromagnetic order and topologically nontrivial skyrmions in few layers. However, because of the dimensionality effect, such few-layer systems usually exhibit much lower Curie temperature (TC) compared to their bulk counterparts. It is therefore of great interest to explore effective approaches to enhance their TC, particularly in wafer-scale for practical applications. Here, we report an interfacial proximity-induced high-TC 2D FM Fe3GeTe2 (FGT) via A-type antiferromagnetic material CrSb (CS) which strongly couples to FGT. A superlattice structure of (FGT/CS)n, where n stands for the period of FGT/CS heterostructure, has been successfully produced with sharp interfaces by molecular-beam epitaxy on 2-inch wafers. By performing elemental specific X-ray magnetic circular dichroism (XMCD) measurements, we have unequivocally discovered that TC of 4-layer Fe3GeTe2 can be significantly enhanced from 140 K to 230 K because of the interfacial ferromagnetic coupling. Meanwhile, an inverse proximity effect occurs in the FGT/CS interface, driving the interfacial antiferromagnetic CrSb into a ferrimagnetic state as evidenced by double-switching behavior in hysteresis loops and the XMCD spectra. Density functional theory calculations show that the Fe-Te/Cr-Sb interface is strongly FM coupled and doping of the spin-polarized electrons by the interfacial Cr layer gives rise to the TC enhancement of the Fe3GeTe2 films, in accordance with our XMCD measurements. Strikingly, by introducing rich Fe in a 4-layer FGT/CS superlattice, TC can be further enhanced to near room temperature. Our results provide a feasible approach for enhancing the magnetic order of few-layer 2D FMs in wafer-scale and render opportunities for realizing realistic ultra-thin spintronic devices.  相似文献   

9.
Magnetic loss in remanent state ferrites1 has generally been described through the artifice of a magnetic loss tangent (tanδm = μ?μ′). This characterization is not directly relatable to intrinsic material parameters. The results presented in this paper indicate that magnetic loss in the remanent state can be related to intrinsic material parameters by describing the ferrite mathematically by a complex “average” permeability tensor. The “average” permeability includes the effects of magnetocrystalline anistropy, remanent magnetization, linewidth and an average demagnetizing field appropriate to the distribution of magnetic domains. Experimental examples are given showing that excellent agreement is obtained between theoretically predicted and measured losses.  相似文献   

10.
BackgroundHydroxycinnamic acids and some of their derivatives are molecules with interesting biological activities; for instance, hydroxylated hydroxycinnamic esters have proved to have antifungal properties, and thus the generation of these molecules is of industrial importance. In this study, the direct esterification capacity of the pure recombinant type B feruloyl esterase from Aspergillus terreus (AtFAE B) was evaluated by its ability to catalyze the synthesis of isobutyl o-coumarate, an interesting antifungal molecule. A ternary solvent system (isooctane/isobutanol/water) was employed to improve the synthesis of isobutyl o-coumarate, assessing different substrate concentrations, enzyme load, water percentages and pH and temperature values.ResultsAtFAE B showed the highest initial rate at 18% (v/v) isobutanol and 50 mM o-coumaric acid, 0.04 mg/ml of enzyme, 4% (v/v) water without buffer and 40°C. AtFAE B half-lives at 30°C, 40°C and 50°C were 16.5 h, 1.75 h and 3.5 min, respectively. Thus, we decided to evaluate the bioconversion yield at 30°C, where the enzyme showed the highest operational stability. At this temperature, we obtained a yield of ~80% after only 8 h of reaction, using a 78:18:4 isooctane:isobutanol:water ternary solvent system, with 50 mM of o-coumaric acid.ConclusionsUnder these improved conditions, the productivity was 1.06 g isobutyl o-coumarate/L*h with a biocatalyst yield of 209.6 kg isobutyl o-coumarate/kg free AtFAE B, demonstrating the promising potential of AtFAE B to accept the non-canonical o-coumaric acid as the substrate and to achieve the synthesis of isobutyl o-coumarate.How to cite: Vega-Rodríguez AD, Armendáriz-Ruiz MA, Grajales-Hernández DA, et al. Improved synthesis of the antifungal isobutyl o-coumarate catalyzed by the Aspergillus terreus type B feruloyl esterase. Electron J Biotechnol 2021;54. https://doi.org/10.1016/j.ejbt.2021.08.001  相似文献   

11.
Honeycomb or triangular lattices were extensively studied and thought to be proper platforms for realizing the quantum anomalous Hall effect (QAHE), where magnetism is usually caused by d orbitals of transition metals. Here we propose that a square lattice can host three magnetic topological states, including the fully spin-polarized nodal loop semimetal, QAHE and the topologically trivial ferromagnetic semiconductor, in terms of the symmetry and k · p model analyses that are material independent. A phase diagram is presented. We further show that the above three magnetic topological states can indeed be implemented in the two-dimensional (2D) materials ScLiCl5, LiScZ5 (Z=Cl, Br) and ScLiBr5, respectively. The ferromagnetism in these 2D materials is microscopically revealed from p electrons of halogen atoms. This present study opens a door to explore the exotic topological states as well as quantum magnetism from p-orbital electrons by means of the material-independent approach.  相似文献   

12.
Exploration of superconductivity in Cr-based compounds has attracted considerable interest because only a few Cr-based superconductors (CrAs, A2Cr3As3 and ACr3As3 (A = K, Rb, Cs, Na)) have been discovered so far and they show an unconventional pairing mechanism. We report the discovery of bulk superconductivity at 5.25 K in chromium nitride in Pr3Cr10-xN11 with a cubic lattice structure. A relatively large upper critical field of Hc2(0) ∼ 12.6 T is determined, which is larger than the estimated Pauli-paramagnetic pair-breaking magnetic field. The material has a large electronic specific-heat coefficient of 170 mJ K−2 mol−1—about 10 times larger than that estimated by the electronic structure calculation, which suggests that correlations between 3d electrons are very strong in Pr3Cr10-xN11, and thus quantum fluctuations might be involved. Electronic structure calculations show that the density of states at the Fermi energy are contributed predominantly by Cr 3d electrons, implying that the superconductivity results mainly from the condensation of Cr 3d electrons. Pr3Cr10-xN11 represents a rare example of possible unconventional superconductivity emerging in a 3D system with strong electron correlations. Nevertheless, clarification of the specific pairing symmetry needs more investigation.  相似文献   

13.
BackgroundIron magnetic nanoparticles have attracted much attention. They have been used in enzyme immobilization because of their properties such as product is easily separated from the medium by magnetic separation. The present work was designed to immobilize horseradish peroxidase on Fe3O4 magnetic nanopraticles without modification.ResultsIn the present study, horseradish peroxidase (HRP) was immobilized on non-modified Fe3O4 magnetic nanoparticles. The immobilized HRP was characterized by FT-IR spectroscopy, scanning electron microscopy, and energy dispersive X-ray. In addition, it retained 55% of its initial activity after 10 reuses. The optimal pH shifted from 7.0 for soluble HRP to 7.5 for the immobilized HRP, and the optimal temperature shifted from 40°C to 50°C. The immobilized HRP is more thermostable than soluble HRP. Various substrates were oxidized by the immobilized HRP with higher efficiencies than by soluble HRP. Km values of the soluble and immobilized HRP were 31 and 45 mM for guaiacol and 5.0 and 7.0 mM for H2O2, respectively. The effect of metals on soluble and immobilized HRP was studied. Moreover, the immobilized HRP was more stable against high concentrations of urea, Triton X-100, and isopropanol.ConclusionsPhysical immobilization of HRP on iron magnetic nanoparticles improved the stability toward the denaturation induced by pH, heat, metal ions, urea, detergent, and water-miscible organic solvent.  相似文献   

14.
Reducing the NOx emissions from Diesel engines remains as a challenging issue as the emission standards for Diesel engine powered vehicles have become more stringent than ever before. Urea-based selective catalytic reduction (SCR) systems have emerged as a promising technique in addressing this issue. However, the SCR performance in terms of NOx reduction and ammonia slip continues as an ongoing challenge due to the engine exhaust gas temperature variations, Diesel emission characteristics (especially high NO/NO2 ratio), and immature SCR controls. The purpose of this study is to improve the SCR performance by feeding the SCR system with exhaust gas having the desired NO/NO2 ratio. The proposed complete active NO/NO2 ratio control consists of a low-level adaptive NO/NO2 ratio controller and a high-level nonlinear soot mass controller. The low-level controller utilizes the pre-SCR catalysts such as Diesel oxidation catalyst (DOC) to convert part of NO into NO2, while the high-level controller was designed and coordinated with the low-level controller to avoid NO2 reduction through the Diesel particulate filter (DPF). Simulation and experimental results show that the proposed active NO/NO2 ratio control has the potentials of regulating the NO/NO2 ratio to the desired value and thus considerably improving the SCR performance. Simulation results also illustrate that the active NO/NO2 ratio control can enable the SCR system size reduction by a half without a significant sacrifice on the overall tailpipe emission control performance. Such an integrated aftertreatment system control can be instrumental in reducing the cost and improving the performance of SCR systems, especially in low-temperature operations.  相似文献   

15.
An n-port gyrator, terminated by s1-type capacitors in m1-ports, by s2-type capacitors in the next m2-ports and by resistors in the remaining (n-m1-m2)-ports is considered. The determinant of the admittance matrix of the network can be made to yield VSHP (a two-variable Hurwitz polynomial without non-essential singularities of the second kind) under certain conditions involving the sub-determinants of the gyrator matrix. With the gyrator constants as variables and the above conditions as constraints, some 2-D stable low-pass filters have been designed using a suitable optimization procedure. The method is illustrated by examples.  相似文献   

16.
For many experiments in physics and in some engineering applications, it is necessary to produce electron bundles, or as they are often called, “electron beams” of considerable intensities.Various methods have been used for directing a cloud of electrons evaporated from an emitting surface into a beam and then concentrating this beam to a desired degree. The concentration of electron beam in high vacuum depends entirely upon fields of force, either electric or magnetic, while in low vacuum or in rarified rare gas it depends also upon the action of the field of ionized gas molecules.In high vacuum the fields of force act upon the electron beam in a manner similar to the action of lenses upon a beam of light. An improperly shaped field produces effects similar to spherical aberration in poorly corrected lenses; non-uniform velocity of electrons in the beam results in effects similar to chromatic aberration of light.This optical analogy is not perfect.In the case of the electron beam the velocity varies continuously throughout most of the path and indices of refraction employed usually are greater than in the optical case. Moreover, space charge in beams of high intensity limits the concentration attainable; consequently, even theoretically, an electron beam can never be brought up to a mathematical point as in the case of light optics. Many secondary effects are present which complicate the problem still further.In focusing electron beams, both electrostatic and electromagnetic methods have been used extensively. The electrostatic method, however, seems to be preferable, especially when the beam is to be deflected. Precautions should be taken not to destroy the focusing of the beam during deflection.  相似文献   

17.
AC Faradaic reactions have been reported as a mechanism inducing non-ideal phenomena such as flow reversal and cell deformation in electrokinetic microfluidic systems. Prior published work described experiments in parallel electrode arrays below the electrode charging frequency (fc), the frequency for electrical double layer charging at the electrode. However, 2D spatially non-uniform AC electric fields are required for applications such as in plane AC electroosmosis, AC electrothermal pumps, and dielectrophoresis. Many microscale experimental applications utilize AC frequencies around or above fc. In this work, a pH sensitive fluorescein sodium salt dye was used to detect [H+] as an indicator of Faradaic reactions in aqueous solutions within non-uniform AC electric fields. Comparison experiments with (a) parallel (2D uniform fields) electrodes and (b) organic media were employed to deduce the electrode charging mechanism at 5 kHz (1.5fc). Time dependency analysis illustrated that Faradaic reactions exist above the theoretically predicted electrode charging frequency. Spatial analysis showed [H+] varied spatially due to electric field non-uniformities and local pH changed at length scales greater than 50 μm away from the electrode surface. Thus, non-uniform AC fields yielded spatially varied pH gradients as a direct consequence of ion path length differences while uniform fields did not yield pH gradients; the latter is consistent with prior published data. Frequency dependence was examined from 5 kHz to 12 kHz at 5.5 Vpp potential, and voltage dependency was explored from 3.5 to 7.5 Vpp at 5 kHz. Results suggest that Faradaic reactions can still proceed within electrochemical systems in the absence of well-established electrical double layers. This work also illustrates that in microfluidic systems, spatial medium variations must be considered as a function of experiment time, initial medium conditions, electric signal potential, frequency, and spatial position.  相似文献   

18.
In many phase-locked loop (PLL) applications, the natural pull-in mechanism is too slow and unreliable, and it must be accelerated. By adding an externally-generated ramp to its control voltage input, the PLL voltage controlled oscillator (VCO) frequency can be swept towards the input reference frequency in an attempt to speed up the pull-in process. This popular acquisition aid has a significant limitation when it is used in a second-order, Type II PLL. If the applied ramp voltage has a slope magnitude greater than (alternatively, less than) some value Rm, the PLL state can (alternatively, cannot) sweep past the desired lock point, resulting in a phase lock failure (alternatively, success). In general, the maximum sweep rate magnitude Rm can be computed by using a numerical integration-and-search procedure that is described in the PLL literature. A special case exists for a second-order, Type II PLL that incorporates a triangular-characteristic phase detector (with logic-level binary input signals). For this case, it is possible to develop an exact, closed-form expression for Rm, the main result of this paper. For a range of loop parameters most often used in applications, Rm values are computed by using the exact formula, and these are used in two ways. First, they are used to validate the previously-mentioned numerical integration-and-search procedure. Second, they are compared to maximum sweep rate values computed for a PLL that utilizes a sinusoidal phase detector to show that the triangular-phase-detector PLL can be swept significantly faster than the sinusoidal-phase-detector loop.  相似文献   

19.
By means of Mawhin's continuation theorem, we study a kind of fourth-order p-Laplacian neutral functional differential equation with a deviating argument in the form:
(φp(x(t)−cx(tδ)))=f(x(t))x(t)+g(t,x(tτ(t,|x|)))+e(t).  相似文献   

20.
张利  雷军  张小雷 《资源科学》2012,34(1):42-49
本文根据IPCC碳排放计算指南缺省值计算了新疆1952年-2008年的碳排放量,系统分析了新疆碳排放总量、碳排放结构、碳排放强度的变化,并对新疆碳排放进行阶段划分,最后应用对数平均迪氏指数法(Logarithmic Mean Divisia Index)对碳排放量进行因素分解,定量分析了碳排放不同阶段各影响因素对碳排放的作用程度。结果表明:①1952年-2008年,新疆CO2排放总量和人均CO2排放量不断上升,万元GDP碳排放水平则呈先上升后降低的"倒V"型曲线,煤炭消费是碳排放的主要来源,第二产业能源消费产生的CO2排放量比重最大;②新疆碳排放经历了五个阶段,当前处于经济和碳排放快速增长阶段;③碳排放不同阶段各影响因素的作用程度不同。总体来看,经济增长是碳排放量增加的主要推动因素;能源消费强度的降低(升高)也是促使碳排放减少(增加)的主要因素;能源消费结构由于变化不大,对碳排放的影响很小;计划生育政策实施以来,人口增长对碳排放量增长的推动力逐渐减弱。能源消费强度又进一步受到产业结构和各产业能耗强度的影响,其中,第二产业能耗强度和第二产业产值比重是影响能源消费强度最主要的影响因素。  相似文献   

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