ZSM-5型分子筛强化水吸收CO_2

在难溶气体吸收体系中加入第3分散相粒子是强化传质过程的一个重要手段,文中采用恒温搅拌釜对ZSM-5型分子筛/水浆料强化CO2的吸收过程进行了实验研究,考察了硅铝摩尔比(120,150,360)、固含率和气相CO2体积分数对增强因子的影响。结果表明:随着分子筛硅铝摩尔比的增加,其疏水性增强,增强因子随之增大;随着分子筛固含率的增加,气液界面处颗粒的覆盖率增大,增强因子迅速增大,当气液界面处颗粒的覆盖率逐渐接近最大覆盖率时,则增强因子逐渐趋于恒定值;随着气相CO2体积分数的增加,溶质在溶液中的扩散作用逐渐增强,而分子筛颗粒输运作用逐渐减弱,增强因子减小。针对分散相微粒增强难溶气体的吸收过程,提出了一个三维非均相传质模型,计算结果和实验数据吻合良好。     

气液固三相外环流反应器相含率分布与气液流动结构

结合电阻层析成像和差压法,以粒径3 mm的聚氨酯(密度1110 kg/m3)和粒径0.5, 1, 3 mm的玻璃珠(密度2460 kg/m3)为固相、空气为气相、水为液相,在直径0.09 m、高3.1 m的气液固三相气升式外环流反应器中考察了固相颗粒密度、粒径、固相含率对上升管和下降管中气含率的影响. 结果表明,当玻璃珠粒径为0.5和1 mm、表观气速ug>0.10 m/s时环流反应器可达到充分发展段. 以玻璃珠为固相时,气含率随固相含量和粒径增大而增大,从层析图像可见,在r/R=0~0.2处出现非导电相的极大值,且加入大颗粒的下降管中气固含率明显大于加入小颗粒的. 根据电阻层析成像的虚拟像,给出了时间序列的气固混合相的流动特征.     

水溶液中甲苯分散相增强难溶气体吸收

利用难溶气体的物理吸收过程,在具有恒定气液界面面积的吸收装置中研究了常压和室温条件下分散液相(甲苯)对气液传质的增强作用。通过测定气相(丙烷和氢气)压力随时间的变化,计算出液侧传质系数和传质增强因子。试验发现,当传质组分在分散液相与连续液相内的分配系数较大,或在两相间的相对扩散系数较大,且分散相形成的液滴较小时,加入分散液相可显著增强气液传质;增强因子随分散液相含率的增大而增大,但增大幅度逐渐减小;当气体在纯水中的传质系数增大时,同等条件下分散相对气液传质的增强作用减小。     

分布板开孔率对气固流化床流动特性的影响

在内径0.14 m,高1.6 m的气固流化床中,以空气和流化催化裂化颗粒为气相和固相,采用PV-6A型光纤测速仪和U形管压差计分别测定三种不同开孔率分布板时的颗粒浓度分布和分布板压降,同时应用流体力学软件Fluent 6.2分别对三种不同开孔率分布板压降,径向固含率分布进行了模拟计算,模拟结果与实验值吻合较好.研究结果显示,分布板压降随开孔率的增大而减小,分布板开孔率大于0.86%后对压降影响较小;径向固含率波动随开孔率的增大而增大,开孔率0.46%的分布板径向固含率分布曲线波动最小,气固分布最均匀.     

重力沉降+旋风分离组合装置分离性能的研究

研究了重力沉降+旋风分离组合装置的初始压降及其分离性能。结果表明:组合装置的初始压降随进口气速的增加而明显增大;在过滤状态下,进口含尘浓度对压降的影响基本可以忽略不计,压降随进口气速的增加明显升高;当进口气速较低(v=5m/s)时,分离效率随进口含尘浓度的增大而增大;当进口气速较高(v≥10m/s)时,分离效率随进口含尘浓度的增大而下降。同时,建立了重力沉降+旋风分离组合装置压降和分离效率的计算模型。     

液相射流吸收耦合气相旋流分离烟气脱硫

在传统的除雾型旋风分离器基础上进行改进,使其同时具备液相射流、气液吸收反应以及气液分离功能,并将这一新型旋风分离器用于烟气脱硫实验。实验中气相为含SO₂烟气,液相为NaOH或Na₂CO₃碱液吸收剂,通过调节吸收剂浓度、烟气含硫浓度、烟气喷射速度、吸收剂喷射速度、吸收剂固含率等参数得到其相应脱硫率的变化。实验研究表明：脱硫率随吸收剂浓度的增加先增加,达到一定浓度后脱硫率几乎不变;脱硫率随SO₂进口浓度的升高而下降;随进口气速的增大,脱硫率也一定程度增大;随液体喷射速度的增加脱硫率先增大,增大到一定程度后脱硫率趋于不变;NaOH作为吸收剂所得最佳脱硫率可达85%,Na₂CO₃作为吸收剂,最佳脱硫率可达77%;当其他参数一定时,加入一定量的CaCO₃固体微粒,可以提高脱硫效率1%~2%。该液相射流吸收耦合气相旋流分离装置不仅脱硫效率高,而且脱硫剂损失少,投资成本与运行维护费用均低于相同处理量的烟气脱硫塔,具有良好的应用前景。     

高长径比三相内环流反应器中相含率的分布研究

在长径比为22的三相内环流反应器中,常温常压下,以空气-水-石英砂为物系,根据无因次准数建立了气含率、固含率的预测模型,考察了在不同粒径下上升区气含率、下降区气含率和上升区固含率、下降区固含率随表观气速的变化规律和不同固体体积分数下轴向固含率的分布情况。结果表明：不同粒径下上升区和下降区气含率均随表观气速的增大而增大;当粒径（ds）≤0．3mm时,上升区固含率随表观气速的增加呈平缓趋势,下降区固含率随表观气速的增加而增加,当0．3mm〈d。≤1．2mm时,上升区固含率随表观气速的增加而呈先下降后增加的趋势,下降区固含率随表观气速的增加而下降;不同固体体积分数下的固体颗粒的固含率随着轴向高度的增大而变化平缓,能够均匀的分布在反应器中;气含率和固含率的计算值和实验值吻合较好,其平均相对误差分别为6．32％、4．56％。     

微通道内单乙醇胺水溶液吸收CO_2/N_2混合气的传质特性

采用高速摄像仪对400μm×400μm T形微通道内单乙醇胺(MEA)水溶液吸收混合气中CO_2过程的气液两相流及传质特性进行了实验研究,微通道内的压力降采用压力传感器进行测量。考察了弹状流型下气液两相流量及MEA浓度对压力降、比表面积和传质性能的影响。结果表明,当MEA浓度不变,气液两相流量增大时,压力降、比表面积、传质系数、体积传质系数和增强因子均增大,并逐渐趋于恒定。当气液流量不变,MEA浓度增大时,压力降、传质系数、体积传质系数和增强因子增大,但比表面积减小。实验条件下,压力降范围为2.00~5.23 kPa,化学吸收过程的传质系数范围为7.74×10~(-4)~2.97×10~(-3) m·s~(-1)。对于伴有快速化学反应的传质过程,以Sherwood数、Reynolds数、Schmidt数及增强因子为变量建立了体积传质系数的预测关联式,平均偏差为5.09%,具有良好的预测性能。     

二维喷嘴内稠密气固射流稳定性实验

利用高速摄像仪对二维喷嘴内稠密气固射流稳定性进行了实验研究,考察了颗粒粒径、料仓压力以及喷嘴收缩角等因素对射流流动模式及稳定性的影响。结果表明：对于颗粒粒径为78μm的气固射流,随着料仓压力的增大,射流出口速度增大,射流固含率降低,在料仓压力≥0.03MPa、射流速度≥4.82m/s、射流固含率≤0.168时,喷嘴内稠密气固射流出现气泡型的不稳定流动模式;随着颗粒粒径的增大,气固射流固含率降低,喷嘴内稠密气固射流从气泡模式转变为颗粒团不稳定流动模式;改变喷嘴收缩角对射流不稳定模式影响不大。利用微型压力传感器对喷嘴直管不同位置压力进行测量,结果表明压力脉动主要是由于气固射流中气泡及颗粒团的产生及演变导致的。研究表明,随着料仓压力增大,颗粒在喷嘴内向下运动过程中压降增加,渗透进颗粒流的气体分率增加,将导致喷嘴内气固相互作用增强,进而引起气固射流不稳定。     

连续内环流三相反应器局部流动特性

在φ200 mm×2500 mm连续内环流三相反应器内,考察了空气 水 玻璃珠体系反应器内局部流动参数随操作条件的变化规律。结果表明,导流筒内截面平均气含率随表观气速的增大而增大,较之气液两相流,在低固含率时,加入固体对气含率影响不明显,而在较高固含率下,气含率有明显降低,但固体再增加时对气含率变化影响不大。在较低表观气速下,进料浆速对导流筒内气含率轴向分布趋势有一定的影响,但在较高表观气速下影响不大,导流筒内的气含率大于环隙内的气含率且随气速增大差别更加明显,浆相连续有利于气相分散并增大环隙内的气含率。导流筒内循环浆速径向分布呈抛物状,中心高、近壁处低,受进料浆速和入口固含率影响都不大。浆相循环强度最低为20,高可达180。固含率轴、径向分布受表观气速和进料浆速的影响,固含率轴、径向分布基本均匀,随进料浆速增加,反应器内固含率降低。     

Preparation and properties of poly(Nε,Nε-dicarboxymethyl-l-lysine)

A new ampholytic homopolypeptide, $\text{poly}\text{(N}{}^{\mathrm{\epsilon }}\text{,N}{}^{\mathrm{\epsilon }}\text{-}\text{dicarboxy-methyl-}\text{l}\text{-lysine}\text{)}$, which has one tertiary amino and two carboxyl groups in the side chain has been derived from a hydrochloride salt of poly(L-lysine). The polymer in aqueous solution seems to be in the coil form with locally extended structure (LES) at neutral pH. In both the acidic and alkaline regions, the molar ellipticity of the polymer changes as a result of change in net charge on the side chain. The conformational changes may be from the coil with LES to other coiled forms. 5–7 M NaClO₄ and 80% aqueous methanol induce the α-helix in the polymer at neutral pH. Divalent cations, Cu²⁺ and Ca²⁺, do not induce any remarkably ordered structures such as α-helix or β-structure in the polymer in aqueous solution at any pH. Ultraviolet absorption studies show an absorption peak of the polymer-Cu²⁺ complex near 240 nm. Dependence of the peak intensity on pH at various q values ($\text{q =}\text{[}\text{Cu}{}^{\mathrm{2+}}\text{]}\text{[}\text{residue}\text{]}$) indicates the two steps of the complex formation. At q less than 0.64, the formation is described only with the first step. An average coordination number for Cu²⁺ at the first step was calculated to be about 2 by the method of Mandel and Leyte. The association constant of Cu²⁺ with the residue at the step was determined from the absorption data to be far smaller than that for the Cu²⁺-EDTA complex. The second step of the formation occurs in the case of large q but the absorption data for the second step cannot be obtained exactly due to precipitation.     

Wet Milling of Fe/Al/Al2O3 and Fe2O3/Al/Al2O3 Powder Mixtures

Wet milling of Al₂O₃-aluminide alloy (3A) precursor powders in acetone has been investigated by milling Fe/Al/Al₂O₃ and Fe₂O₃/Al/Al₂O₃ powder mixtures. The influence of the milling process on the physical and chemical properties of the milled powders has been studied. Particle refinement and homogenization were found not to play a dominant role, whereas plastic deformation of the metal particles leads to the formation of dislocations and a highly disarranged polycrystalline structure. Although no chemical reactions among the powder components in Fe₂O₃/Al/Al₂O₃ powder mixtures were observed, the formation of a nanocrystalline, ordered intermetallic FeAl phase in Fe/Al/Al₂O₃ powder mixtures caused by mechanical alloying was detected. Chemical reactions of Fe and Al particle surfaces with the atmosphere and the milling media lead to the formation of highly porous hydroxides on the particle surfaces. Hence the specific surface area of the powders increases, while the powder density decreases during milling. The fraction of Fe oxidized during milling was determined to be 0.13. The fraction of Al oxidized during milling strongly depends on the metal content of the powder mixture. It ranges between 0.4 and 0.8.     

Sintering of Si3N4-Y2O3-Al2O3

Sintering kinetics of the system Si₃N4-Y2O₃-Al₂O3 were determined from measurements of the linear shrinkage of pressed disks sintered isothermally at 1500° to 1700°C. Amorphous and crystalline Si₃N₄ were studied with additions of 4 to 17 wt% Y₂O₃ and 4 wt% A1₂O₃. Sintering occurs by a liquid-phase mechanism in which the kinetics exhibit the three stages predicted by Kingery's model. However, the rates during the second stage of the process are higher for all compositions than predicted by the model. X-ray data show the presence of several transient phases which, with sufficient heating, disappear leaving mixtures of β ' -Si₃N₄ and glass or β '-Si₃N₄, α '-Si₃N₄, and glass. The compositions and amounts of the residual glassy phases are estimated.     

Participation of lewis base on vinyl chloride polymerization with Al(C2H5)3CCl4 catalyst system

The polymerization of vinyl chloride has been investigated using an $\text{Al}\text{(}\text{C}{}_2\text{H}{}_5\text{)}{}_3\text{CCl}{}_4$ catalyst system in the presence of various Lewis bases. Effective Lewis bases are γ-butyrolactone, diglyme and diethylenetriamine which are multidentate. The rate of polymerization is dependent not only on the basicity of the Lewis base used but also on a coordination number of one. The latter is the predominant factor. For the effect of polymeric amines, a tentative hypothesis is discussed.     

Synthesis and Characterization of Ti0.33Ta0.33Nb0.33C and Ti0.33Ta0.33Nb0.33CxN1-x Whiskers

Ta_0.33Ti_0.33Nb_0.33C and Ta_0.33Ti_0.33Nb_0.33C _x N_{1− x} whiskers were synthesized via a carbothermal vapor-liquid-solid growth mechanism in the temperature range 900°-1450°C in Ar or N₂. The optimum temperature was 1250°C. Whiskers were obtained in a yield of 70-90 vol%. The whiskers were 0.5–1 µm in diameter and 10–30 µm in length. The starting materials that produced the highest whisker yield were: TiO₂, Ta₂O₅, Nb₂O₅, C, Ni, and NaCl. C was added to reduce the oxides, and Ni to catalyze whisker growth. NaCl was used as a source of Cl for vapor-phase transportation of Ta and Nb oxochlorides and Ti chlorides to the catalyst. The catalyst metal was recycled several times during the synthesis and was transported as NiCl₂( g ) according to thermodynamic calculations. The rate of formation and the chemical composition of the whiskers depended on the synthesis temperature, the choice of catalyst, and the atmosphere. At low temperatures, the whiskers were enriched in Nb and Ta, whereas the Ti content increased with increased synthesis temperature.