生物质热解液化装置输料系统特性试验

输料装置是生物质热解液化工艺系统中不可或缺的设备之一;而连续稳定的输料特性是保证生物质热解液化工艺过程的关键技术。介绍了一种实验采用的生物质输料系统;并以不同粒径的锯末、稻壳、麦麸、玉米粒为生物质代表原料,实验研究了各种因素对输料量的影响规律。实验结果对实现生物质连续可靠的热解液化生产过程具有重要的参考价值。

不同种类生物质输送量的理论预测方法与实验回归公式

连续稳定地向生物质热解液化工艺系统输送适量的生物质原料是实现生物油连续生产的必要前提条件,而生物质种类及粒径分布千差万别,如何较为准确地预测不同生物质的输送量是至关重要的。本文以不同粒径的四种典型生物质原料为代表,实验测试了生物质的堆积密度及输料量的变化规律。结合输料系统特点,提出了理论预测输料量的方法,通过对实验数据进行多元线性回归处理,得到了物理意义清晰的实验回归公式。对比表明,理论公式、实验回归公式均与实验结果吻合良好,绝大部分数据点落在±10%的误差线内。本文的研究结果对于生物质热解液化工艺方法的研究具有重要参考价值。

Numerical simulations of water flow and contaminants transport near mining wastes disposed in a fractured rock mass

A numerical tool, called Hydro-Geosphere, was used to simulate unsaturated water flow and contaminants migration around an open pit filled with mining wastes. Numerical simulations had been carried out to assess the influence of various factors on water flow and solute transport in and around the surface openings including recharge, properties of the waste material and presence of fractures in the surrounding rock mass. The effect of the regional hydraulic gradient was also investigated. The analyses were conducted by simulating various 2D cases using experimentally obtained material properties and controlled boundary conditions. The effects of the hydrogeological properties of the filling material(i.e., water retention curve and hydraulic conductivity function), fracture network characteristics and conductivity of the joints were assessed. The results illustrate that fractures control water flow and contaminants transport around the waste disposal area. A fracture network can desaturate the system and improve the regional gradient effect.

Teleportation of N-qubit W State without Bell-State Measurement via Selective Resonant Interaction in Cavity QED

We present a scheme in which the N-atom W state is teleported by employing the selective interactionof a cavity field with a driven three-level atom in the A configuration and detecting a single atom in one of the groundstates.The long-lived W state is teleported from atom A to atom B when the atoms B and A are sent through acavity successively and atom A is then detected.The advantage is that the present one does not involve the Bell-statemeasurement and is robust against the atomic spontaneous emission.

Optoelectronic properties of new functionalized heteroleptic iridium complex

A new functionalized heteroleptic iridium complex coordinated with 1-phenylisoquinoline （1-piq） and a functionalized fl-diketone （G1）, Ir（1-piq）2G1, was synthesized and characterized by 1H-NMR, mass spectrometry and elemental analysis. The larger conjugation of the replacement of acetylacetone （acac） by a functionalizedβ-diketonate ligand led to a significant decrease in the HOMO level toward vacuum level, while Ir（1-piq）2G1 and Ir（1-piq）2（acac） showed red phosphorescent emissions of about 620 nm in dichloromethane solution. The phosphorescent polymer light-emitting devices were achieved, with the complexes incorporated with polyfluorene （PFO） as a host polymer doped with 30% of 5-（4-biphenylyl）-2-（4-tert-butylphenyl）-1,3,4-oxadiazole （PBD） as electron transport material. The energy transfer mechanism of the devices was also discussed. The lower EL performance of Ir（1-piq）2G1 is ascribed to the inter-ligand energy transfer, indicating that it is important to control the energy level of the cyclometalated and ancillary ligands.

Generation of electricity from CO_2 mineralization: Principle and realization

Current CO2 reduction and utilization technologies suffer from high energy consuming. Thus, an energy favourable route is in urgent demanding. CO2 mineralization is theoretically an energy releasing process for CO2 reduction and utilization, but an approach to recovery this energy has so far remained elusive. For the first time, here we proposed the principle of harvesting electrical energy directly from CO2 mineralization, and realized an energy output strategz1 for CO2 utilization and reduction via a CO2-mineralization fuel cell （CMFC） system. In this system CO2 and industrial alkaline wastes were used as feedstock, and industrial valuable NaHCO3 was produced concomitantly during the electricity generation. The highest power density of this system reached 5.5 W/m2, higher than many microbial fuel cells. The maximum open circuit voltage reached 0.452 V. Moreo- ver, this system was demonstrated viable to low concentration CO2 （10%） and other carhonation process. Thus, the existing of an energy-generating and environmentally friendly strategy to utilize CO2 as a supplement to the current scenario of CO2 emis- sion control has been demonstrated.

Superstructured α-Fe2O3 nanorods as novel binder-free anodes for high-performing fiber-shaped Ni/Fe battery

Fiber-shaped energy storage devices are indispensable parts of wearable and portable electronics.Aqueous rechargeable Ni/Fe battery is a very appropriate energy storage device due to their good safety without organic electrolytes, high ionic conductivity, and low cost. Unfortunately, the low energy density,poor power density and cycling performance hinder its further practical applications. In this study, in order to obtain high performance negative iron-based material, we first synthesized a-iron oxide(α-Fe2O3) nanorods(NRs) with superstructures on the surface of highly conductive carbon nanotube fibers(CNTFs), then electrically conductive polypyrrole(PPy) was coated to enhance the electron, ion diffusion and cycle stability. The as-prepared α-Fe2O3@PPy NRs/CNTF electrode shows a high specific capacity of 0.62 Ah cm-3 at the current density of 1 A cm-3. Furthermore, the Ni/Fe battery that was assembled by the above negative electrode shows a maximum volumetric energy density of 15.47 mWh cm-3 with228.2 mW cm-3 at a current density of 1 A cm-3. The cycling durability and mechanical flexibility of the Ni/Fe battery were tested, which show good prospect for practical application. In summary, these merits make it possible for our Ni/Fe battery to have practical applications in next generation flexible energy storage devices.

Rational design of perfectly oriented thermally activated delayed fluorescence emitter for efficient red electroluminescence

How to control the dipole orientation of organic emitters is a challenge in the field of organic light-emitting diodes(OLEDs).Herein,a linear thermally activated delayed fluorescence(TADF)molecule,PhNAI-PMSBA,bearing a 1,8-naphthalimide-acridine framework was designed by a doublesite long-axis extension strategy to actively control the dipole orientation.The horizontal ratio of emitting dipole orientation of PhNAI-PMSBA reaches 95%,substantially higher than that of isotropic emitters(67%).This unique feature is associated with the intrinsically horizontal molecular orientation of PhNAI-PMSBA and the good agreement between its transition dipole moment direction and molecular long axis.The PhNAI-PMSBA-based OLED achieves an ultrahigh optical outcoupling efficiency of 43.2%and thus affords one of the highest red electroluminescence with an external quantum efficiency of 22.3%and the Commission International de l’Eclairage 1931 coordinates at around(0.60,0.40).