栲胶脱硫液中总碱和悬浮硫含量测定方法的改进

为准确、快速测定栲胶脱硫液中的总碱和悬浮硫含量,对原测定方法进行了改进。试验证明,改进后的方法完全可满足生产控制分析要求。     

A/O法废水处理碱源的研究与实践

从理论到实践阐述了以具有价格优势的 Na OH替代 Na2 CO3做碱源 ,解决 A / O法运行成本高的问题。     

中小型造纸厂黑液碱回收探讨

对中小型造纸厂黑液碱回收，到目前为止尚无被公众认可的成熟技术。借鉴前人的经验和教训，从另一个角度思考造纸黑液的酸析残液中碱分离技术，采用环烷酸萃取技术，能理想地将酸析残液中Na^ 与可溶性有机物进行分离，分离效率达60％以上。该法优点是操作简单，生产成本低，工艺稳定性好；缺点是调配成的萃取剂异味较重，Na^ 回收率有待进一步提高。     

碱溶透析和酸析处理对碱木质素物化性质和Pb2+去除性能的影响

采用XPS、静态接触角、颗粒表面电荷、扫描电镜、官能团分析等方法来研究碱木质素经过碱溶透析和碱溶酸析处理后的物化性质的差异，探讨碱木质素分子聚集程度对Pb²⁺去除性能的影响。结果表明，碱溶透析木质素的比表面积是碱溶酸析木质素的4.77倍，碱溶透析样品较酸析样品的表面氧含量高48%、水/木质素薄膜的静态接触角低13°，反映出碱溶透析处理后的木质素比碱溶酸析处理后的木质素分子聚集程度低、分子链疏松、羧基和羟基等含氧官能团裸露程度增加。碱溶透析处理后的木质素与Pb²⁺的静电作用增强，对Pb²⁺的去除能力显著提高。Pb²⁺浓度为100 mg·L^-1时，碱溶透析木质素对Pb²⁺的去除量达136 mg·g^-1，去除率为81.8%，且去除性能受体系pH的影响小。与化学改性和表面功能化相比，利用碱溶透析处理以提高木质素对Pb²⁺的去除性能具有操作简单、无毒、能耗低的优点。     

镁质低品位铁镍硫化矿的活化工艺及机理

细菌浸出是镁质低品位铁镍硫化矿的潜在处理方案之一。针对该矿石浸出活性较低的问题,研究了硫酸预浸出和硫酸铵焙烧预浸出2种活化方案,并与细菌直接浸出(空白试验)做了比较。结果表明,2种活化方案都有利于金属回收,但硫酸铵焙烧预浸出方案的活化效果更优:浸出时间为8 d时,Ni、Cu和Mg的浸出率分别为90.2%、89.56%和61.19%,分别高于硫酸预浸出方案2.08%、12.2%和8.95%。矿石中的Mg主要在硫酸铵焙烧预浸出阶段进入溶液,细菌对Mg浸出的影响不大。XRD和能谱分析表明:浸出渣中Ni和Cu的残留量很低,Mg主要存在于难浸出的蛇纹石之中。     

Kinetics study of leaching arsenic from Ni-Mo ore roasting in dust mixture of hydrochloric and sulfuric acids

The kinetics of leaching arsenic from Ni-Mo ore roasting dust was investigated. The effects including leaching temperature, particle size of the smelter dust, stirring speed, the coefficient β（the molar ratio of sodium chlorate to arsenic in the smelter dust） and the initial H＋ concentration on leaching arsenic were studied. The results indicate that the leaching of arsenic increases sharply with the decrease of particle size. The orders of reaction with respect to H＋ concentration and particle size are determinted to be 1.136 and 1.806, respectively. The leaching of arsenic reaches 99% under experimental conditions, the apparent activation energy is determined to be 11.157 kJ/mol, which is consistent with the values of activation energy for diffusion model The kinetics equation of leaching arsenic from the roasting dust could be expressed by a semi-empirical equation as 1-2/3η （1 -η）^2/3 = k0（c[H＋]）^1.136ro^-1.806 exp[（-11157 /RT）t].     

Evaluating the role of composition and local structure on alkali out-diffusion in glasses for thin-film solar cells

The presence of alkali ions has reportedly improved the performance of CIGS/CZTS–based thin-film solar cells. The out-diffusion of the alkali ion, in particular, Na, from the glass substrate offers a facile scalable route of supplying the alkali ions during the growth of the absorber layer. In this work, we demonstrate the diffusion of different alkali ions (Li/Na/K) from composition tuned glasses with intentionally incorporated excess alkali ions into a thin Mo film, typically used as a bottom electrode in solar cells. We also evaluate the physical, mechanical, and thermal properties of the glasses for suitability as a substrate in thin-film deposition. The out-diffusion of alkali ions to the overlayer is found to be critically influenced by the composition and the local structure of the glasses. The Na ions exhibit the highest extent of diffusion among the alkali ions present in glass substrates, while that for the K-ions is the lowest. For the glasses with mixed alkali ions, the presence of Li facilitated the out-diffusion of Na, whereas K ions appear to inhibit the same. Differently with the existing reports, we show that the activation energy and the presence of Ca ions as additional modifiers play a crucial role in the transport mechanism of the ions. In addition, the synthesized glasses exhibit hardness of the order 5-7 GPa, density ~2.55 g cm^-3. The glass transition temperature lies between 535 and 580°C and the coefficient of thermal expansion 8.5-10 ppm/K, which is highly suitable for use as substrates in thin-film solar cells.     

Phi zeolite synthesized by template-free method for selective catalytic reduction of NO

Nitrogen oxide (NO_x) is one of the major air pollutants. Using a copper-based zeolite with a chabazite structure (CHA) as a catalyst, the selective catalytic reduction (SCR) technology can effectively remove NO_x. This work introduces a low silica CHA type zeolite with structural defects (zeolite Phi, with Si/Al of 4.7). The zeolite Phi is synthesized through a hydrothermal method without adding any template, which is low-cost and environment-friendly. The Cu-exchanged Phi is abundant of surface acidity and isolated Cu²⁺, showing a superior low-temperature activity, a wide work temperature window and a good hydrothermal stability. The presence of Na or Mg decreases the surface acidity and isolated Cu²⁺. The hydrothermally aged Na,Cu/Phi and Mg,Cu/Phi present different levels of framework collapse, which correspondingly induces catalyst deactivation.     

硫酸装置尾气处理改造生产实践

介绍了南化公司2#、3#硫酸尾气处理装置的运行情况及改造实践。针对尾气处理装置存在的副产品难于处理、尾气排放指标达不到特别排放限值、维护成本高等问题,对比了4种硫酸尾气治理工艺的优劣性,结合装置自身特点,确定了采用钠碱法加2级电除雾器工艺对该脱硫系统进行改造。改造后尾气脱硫系统排放SO2质量浓度控制在200 mg/m³以下、硫酸雾质量浓度在5 mg/m³以下,满足《硫酸工业污染物排放标准》排放限值的要求,且硫酸装置尾气脱硫系统实现了与主装置同步稳定运行。     

Erosion-corrosion investigation of high chromium cast irons using newly designed jet type tester

A jet type erosion-corrosion tester was developed for the erosion-corrosion investigation of high-chromium cast irons. During tests the size and the shape of particles in the slurry can be maintained stable. The jet velocity and attack angle can be accurately controlled. The repeatability and ranking consistency of the test results are satisfactory. The test parameters can be adjusted in a wide range, so that the tester can simulate various practical working conditions. Electrochemical test data can be automatically collected and processed. Dynamic polarization curves can be obtained during erosion-corrosion test, which can be used to study the dynamic corrosion characteristics.Two high chromium cast irons were studied in hot concentrated alkaline slurry. The results show that the erosioncorrosion mass loss rate and dynamic corrosion rate of 295Cr26 iron is lower than that of 185Cr13 under the conditions similar to alumyte processing. The mechanism of erosion-corrosion of 295Cr26 and 185Cr13 was studied by using the tester. The interaction between erosion and corrosion was also quantitatively evaluated.