新型喷模剂的研发与应用

在铅酸蓄电池铸板过程中,板栅模具表面需要喷涂一层喷模剂来达到控制板栅重量和厚度的目的,本技术配制溶液a和溶液b,在喷涂板栅模具的过程中配合使用,达到了很好的保温作用,通过铸板实验,生产G25K+单片板栅、G16B-双连片板栅和G8B+三连片板栅,并对板栅重量厚度进行测量,发现新型喷模剂的使用能够很好地控制板栅的重量和厚度,增强板栅的一致性,延长喷模剂的使用时间,提高生产效率。

离模剂使用量对LED产品的影响

在LED封装过程中,大家往往很容易忽略一些辅料对LED产品质量的影响,从而造成不良率过高,良品率低,成本增加。本文主要讲述辅料离模剂使用量的多少对直插式LED的影响。

离模剂使用量对LED产品的影响

在LED封装过程中,大家往往很容易忽略一些辅料对LED产品质量的影响,从而造成不良率过高,良品率低,成本增加。本文主要讲述辅料离模剂使用量的多少对直插式LED的影响。

新型早强带模注浆材料配方设计及拱顶带模注浆施工工艺研究

二次衬砌背后脱空是指隧道二次衬砌混凝土与初支喷射混凝土之间存在空隙、空洞或不密实的现象。在隧道实体工程质量检测过程中发现,二次衬砌混凝土背后脱空及二次衬砌拱顶不密实现象普遍存在。为了解决上述问题,水电七局试验检测研究院研发了一种新型早强微膨胀带模注浆剂。该注浆剂直接与工程中实际使用的水泥复配组成新型早强带模注浆材料,该注浆材料的施工性能和力学性能不仅能够满足相关规范、设计的要求,也解决了二次衬砌混凝土背后脱空及二次衬砌拱顶不密实现象。新型早强微膨胀带模注浆剂的成功研发不仅较大程度降低了注浆材料的采购成本,也具有较高的技术、经济价值。

In situ electrochemical synthesis of MOF-5 and its application in improving photocatalytic activity of BiOBr

Metal-organic frameworks（MOFs） are important functional materials. MOF-5（IL）（Zn4O（BDC）3（BDC=1,4-benzenedicarboxylate） was in situ synthesized by the electrochemical method using a tunable ionic liquid（IL）, 1-butyl-3-methylimidazolium chloride, as template. The crystallization of distinctly spherical MOF-5（IL） synthsized in ionic liquid by the electrochemical method is attributed to π-π stacking effect, ionic bond, and coordination bond. The analysis results show that the product MOF-5（IL） exhibits better crystallinity and higher thermal stability than MOF-5 generated using the solvothermal method. The cyclic voltammetry reveals that the electrosynthesis reaction is irreversible and controlled by the diffusion. The experiments on methylorange degradation show that the unique structure characteristics of MOF-5（IL） can enhance the photocatalytic ability of Bi OBr. Therefore, MOFs can replace noble metals to improve the photocatalytic properties of bismuth oxyhalide.

Effect of cetyltrimethylammonium bromide on morphology and porous structure of mesoporous hydroxyapatite

The mesoporous hydroxyapatite （HA） was synthesized by hydrothermal method utilizing cationic surfactant cetyltrimethylammonium bromide （CTAB） as template. The crystalline phase, morphology and porous structure were characterized respectively by different detecting techniques. The results reveal that the particles are highly crystalline hydroxyapatite phase. The surfactant has little influence on the morphology of the crystals, but affects the porous structure obviously. The sample without CTAB has a low surface area not exceeding 33 m^2/g, and no distinct pores can be observed by TEM. While the samples obtained with the surfactant get better parameters. Numerous open-ended pores centered at 2-7 nm spread unequally on the surface of the hydroxyapatite nanorods. The N2 adsorption-desorption experiments show type IV isotherms with distinct hysteresis loops, illustrating the presence of mesoporous structure. When the mole ratio of CTAB to HA is 1：2, the sample has the largest surface area of 97.1 m^2/g and pore volume of 0.466 cm^3/g.

Numerical study on dehumidifying process in falling film dehumidifier

A counter flow model of simultaneous heat and mass transfer of a vapor absorption process in a falling film dehumidifier is developed. The governing equations with appropriate boundaries and interfacial conditions describing the dehumidifying process are set up. Calcium chloride is applied as the desiccant. The dehumidifying process between falling liquid desiccant film and process air is analyzed and calculated by the control volume approach. Velocity field, temperature distribution and outlet parameters for both the process air and desiccant solution are obtained. The effects of inlet conditions and vertical wall height on the dehumidification process are also predicted. The results show that the humidity ratio, temperature and mass fraction of salt decrease rapidly at the inlet region but slowly at the outlet region along the vertical wall height. The dehumidification processes can be enhanced by increasing the vertical wall height, desiccant solution flow rates or inlet salt concentration in the desiccant solution, respectively. Similarly, the dehumidification process can be improved by decreasing the inlet humidity ratio or flow rates of the process air. The obtained results can improve the performance of the dehumidifier and provide the theoretical basis for the optimization design, and the ooeration and modulation of the solar liquid desiccant air-conditioning systems.

Framework-solvent interactional mechanism and effect of NMP/DMF on solvothermal synthesis of [Zn_4O(BDC)_3]_8

In order to explore the effect mechanism of solvent on the synthesis of the metal organic framework materials, the microscopic interaction between solvent and framework and the effects of N,N-dimethyl-formamide(DMF) or N-methyl- 2-pyrrolidone(NMP) on solvothermal synthesis of [Zn4O(BDC)3]8 were investigated through a combined DFT and experimental study. XRD and SEM showed that the absorbability of NMP in the pore of [Zn4O(BDC)3]8 was weaker than that of DMF. The thermal decomposition temperature of [Zn4O(BDC)3]8 synthesized in DMF was higher than that in NMP according to TG and FT-IR. In addition, the nitrogen sorption isotherms indicated that NMP improved gas sorption property of [Zn4O(BDC)3]8. The COSMO optimized calculations indicated that the total energy of Zn4O(BDC)3 in NMP was higher than that in DMF, and compared with non-solvent system, the charge of zinc atoms decreased and the charge value was the smallest in NMP. Furthermore, the interaction of DMF, NMP or DEF in [Zn4O(BDC)3]8 crystal model was calculated by DFT method. The results suggested that NMP should be easier to be removed from pore of materials than DMF from the point of view of energy state. It can be concluded that NMP was a favorable solvent to synthesize [Zn4O(BDC)3]8 and the microscopic mechanism was that the binding force between Zn4O(BDC)3 and NMP molecule was weaker than DMF.

不同扫描时间点、心输出量、心率、冠状动脉狭窄程度对冠状动脉管腔内密度衰减梯度的影响

目的评估对比剂注射后不同扫描时间点、不同心输出量、心率、冠状动脉狭窄程度对管腔内密度衰减梯度(tansluminal attenuation gradient,TAG)的影响。方法采用对比剂流量体模和狭窄程度为0%(正常组)和75%(病变组)的两种体模。采用320排CT进行扫描检查。心率分别设置为60、70次·min^(-1),心输出量分别设置为2.0L·min^(-1)和4.5L·min^(-1)。扫描重复时间以0.5s为间隔直至40s(心输出量为2.0L·min^(-1))和25s(心输出量为4.5L·min^(-1))。在相同层面测量CT值,在不同的扫描时间点计算时间密度曲线(time-density-curve,TDC)和TAG值。结果不同的扫描时间点,正常组TAG值的变异较病变组小(心输出量为2.0L·min^(-1)和4.5L·min^(-1));在病变组,与心输出量为2.0L·min^(-1)相比,心输出量4.5L·min^(-1)的TAG值曲线随着不同扫描时间点逐渐改变。结论不论正常组还是病变组,不同扫描时间和心输出量可影响TAG值。

Kinetics of cerium(Ⅳ) and fluoride extraction from sulfuric solutions using bifunctional ionic liquid extractant(Bif-ILE)[A336][P204]

The extraction kinetics of Ce（Ⅳ） and Ce（Ⅳ）-F^- mixture systems from sulfuric solutions to n-heptane solution containing Bif-ILE[A336][P204]（[trialkylmethylammonium][di-2-ethylhewanxylphosphinate]） with a constant interfacial area cell with laminar flow were studied,just to elucidate the extraction mechanism and the mass transfer models.The data were analyzed in terms of pseudo-first-order constants.The effects of stirring speed,specific interfacial area and temperature on the extraction rate in both systems were discussed,suggesting that the extractions were mixed bulk phases-interfacial control process.Supported by the experimental data,the corresponding rate equations for Ce（Ⅳ） extraction system and Ce（Ⅳ）-F^- mixture extraction system were obtained.The experimental results indicated the rate-controlling step.The kinetics model was deduced from the rate-controlling step and consistent with the rate equation.

Synthesis of Li^+ adsorbent(H_2TiO_3) and its adsorption properties

H2TiO3 was obtained from the acid-modified adsorbent precursor Li2TiO3,which was synthesized by a solid-phase reaction between TiO2 and Li2CO3.The extraction ratio of Li＋ from Li2TiO3 was 98.86%,almost with no Ti4＋ extracted.The effects of lithium titanium ratio,calcining temperature and time were investigated on the synthesis of Li2TiO3.Li2TiO3,H2TiO3 and the adsorbed Li＋ adsorbent were characterized by XRD and SEM.The lithium adsorption properties were investigated by the adsorption kinetics and adsorption isotherm.The results indicate that H2TiO3 has an excellent adsorptive capacity for Li＋.Two simplified kinetic models including the pseudo-first-order and pseudo-second-order equations were selected to follow the adsorption processes.The rate constants of adsorption for these kinetic models were calculated.The results show that the adsorption process can be described by the pseudo-second-order equation,and the process is proved to be a chemical adsorption.The adsorption process that H2TiO3 adsorbs Li＋ in LiCl solution well fits the Langmuir equation with monolayer adsorption.

Mechanism of inhibitor ADS-J1 and ADS-J2 binding to HIV-1 gp41

In order to analyze and explain the mechanism of the two small inhibitors （ADS-JI and ADS-J2） binding to HIV-1 gp41, a computational study is carried out to help identifying possible binding modes by docking these compounds onto the hydrophobic pocket on gp41 and characterize structures of binding complexes. The binding interactions of gp41-molecule and free energies of binding are obtained through molecular dynamics simulation and molecular mechanic/Poisson- Boitzmann surface area （ MM/PBSA ） calculation. Specific molecular interactions in the gp41-inhibitor complexes are identified. The present computational study complements the corresponding experimental investigation and helps establish a good starting point tbr further refinement of small molecular gp41 inhibitors.

Reconstruction of the linac photon spectrum based on prior knowledge and the genetic algorithm

In order to derive the linac photon spectrum accurately both the prior constrained model and the genetic algorithm GA are employed using the measured percentage depth dose PDD data and the Monte Carlo simulated monoenergetic PDDs where two steps are involved.First the spectrum is modeled as a prior analytical function with two parameters αand Ep optimized with the GA.Secondly the linac photon spectrum is modeled as a discretization constrained model optimized with the GA. The solved analytical function in the first step is used to generate initial solutions for the GA’s first run in this step.The method is applied to the Varian iX linear accelerator to derive the energy spectra of its 6 and 15 MV photon beams.The experimental results show that both the reconstructed spectrums and the derived PDDs with the proposed method are in good agreement with those calculated using the Monte Carlo simulation.

A Model of Steady-State Convective Combustion of Micropore Propellants

Aim To develop a physical and mathematical model related to micropore para- meters of steady-state convective combustion of micropore propellants(MPP). Methods The micropore parameters were measured by WXT-88 mage analysis apparatus and the convective combustion characteristic of MPP was measured by a large volume closed bomb, respectively. Rasults Statistical physical model of burning in the micropore and granular burning were developed. The burning rate equation of steady-state convective combustion of MPP was obtained. Conclusions This model correlates the convective burning rate with micropores para- meters for the first time,and the calculating values of convective burning rate are in agreement with test results.The model also can be used to estimate the effects of microporous parame- ters, basic mass burning rate, MPP density and pressure in combustion chamber on the convective combustion characteristics of MPP.

Electroless Deposition of Nickel Nanowire and Nanotube Arrays as Supports for Pt-Pd Catalyst for Ethanol Electrooxidation

Nickel nanowire and nanotube arrays as supports for Pt-Pd catalyst were prepared by elec- troless deposition with anodic aluminum oxide template. Pt-Pd composite catalyst was de- posited on the arrays by displacement reaction. SEM images show that the nickel nanowires have an average diameter of I00 nm and the nickel nanotubes have an average inner diameter of 200 nm. EDS scanning reveals that elemental Pt and Pd disperse uniformly on the arrays. Cyclic voltammetry study indicates that the nickel nanotube array loaded with Pt-Pd pos- sesses a higher electrochemical activity for ethanol oxidation than the nickel nanowire array with Pt-Pd.

Liquid drying of BeO gelcast green bodies using ethanol as liquid desiccant

BeO gelcast green bodies were dried by liquid drying method with liquid desiccant ethanol.Effects of ethanol concentration,solids loading and aspect ratio of green body on the moisture and shrinkage of green bodies were studied through measuring mass and dimension.Additionally,liquid drying stress was analyzed and a model of the initial stage drying stress was established.The results show that higher ethanol concentration,lower solids loading and higher aspect ratio of gelcast green bodies increase the drying rate.Increasing the ethanol concentration decreases the shrinkage rate.Liquid drying stress is generated due to a non-uniform drying rate.During the process of liquid drying,the inner drying stress of the green body changes from compressive stress to tensile stress,while the outer drying stress changes from tensile stress to compressive stress.

Preparation, Characterization, Photocatalytic Activity of S and Ag co-Doped Mesoporous Titania Photocatalysts

In order to improve the photocatalytic performance of mesoporous titania under visible light, a series of photocatalysts of S and Ag co-doped mesoporous titania have been successfully prepared by template method using thiourea, AgNO3 and tetrabutyl titanate as precursors and Pluronic P123 （EO20PO70EO20） as template. Scanning electron microscopy （SEM）, X-ray diffraction （XRD）, nitrogen adsorption-desorption measurements, and UV-visible spectroscopy （UV-Vis） were employed to characterize the morphology, crystal structure, surface structure, and optical absorption properties of the samples. The microcrystal of the photocatalysts consisted of anatase phase and was approximately present in the form of spherical particle. The photocatalytic performance was studied by photodegradation methyl orange （MO） in water under UV and visible light irradiation. The calcination temperature and the doping content influenced the photoactivity. In addition, the possibility of cyclic usage of co-doped mesoporous titania was also confirmed, the photocatalytic activity of mesoporous titania remained above 89% of that of the fresh sample after being used four times. It was shown that the co-doped mesoporous titania could be activated by visible light and could thus be potentially applied for the treatment of water contaminated by organic pollutants. The synergistic effect of sulfur and silver co-doping played an important role in improving the photocatalytic activity.

Synthesis, characterization, and catalytic performance of hierarchical ZSM-11 zeolite synthesized via dual-template route

Hierarchical zeolite materials were prepared via one‐pot synthesis of ZSM‐11zeolites with different molar ratios(R)of a mesoporogen,i.e.,cetyltrimethylammonium bromide template(CTAB),to a microporogen,i.e.,tetra‐n‐butylammonium bromide(TBABr).The structures,morphologies,and textural properties of the resultant materials were investigated.Initially,with increasing R,the crystal size of the synthesized product decreased,the number of intercrystalline mesopores increased,and a pure ZSM‐11zeolite phase was present.Then an MCM‐41‐like phase was produced and embedded in the ZSM‐11zeolite phase.Finally,an MCM‐41‐like phase was obtained.The alkalinity had important effects on the physicochemical and textural properties of the prepared samples.A possible mechanism of formation of the hierarchical ZSM‐11zeolite was proposed on the basis of a combination of various characterization results.The role of CTAB varied depending on the R value,and it showed a capping effect,micellar effect,and template effect.These effects of CTAB were synergetic in ZSM‐11synthesis,but they were competitive with the structure‐directing effect of TBABr.In addition,the impact of the acidic properties and porosities of the hierarchical ZSM‐11catalysts on their performances in the alkylation of benzene with dimethyl ether was investigated.?2018,Dalian Institute of Chemical Physics,Chinese Academy of Sciences.Published by Elsevier B.V.All rights reserved.