硫酸钾生产工艺改造

介绍了曼海姆炉的结构特点、生产硫酸钾的反应原理，以及新砌筑曼海姆炉的烘炉程序、生产运行所需条件和生产中曼海姆炉常出现的问题及解决问题的办法，推荐了几种曼海姆炉的工艺改造方案。经过改进后反应炉运行良好，可以延长反应炉的修炉周期，从而延长了反应炉的使用寿命，提高了硫酸钾的产量，节约了大量的修炉费用。     

污水COD超标的影响因素及解决措施

通过对总排污口污水中主要还原性物质逐项进行掩蔽,分析掩蔽前后污水COD值的变化,找出了影响COD的主要因素并提出了改进措施,使排污总口COD值大幅降低。     

PVC生产中的二次水回收工艺改造

介绍了在PVC生产过程中产生的蒸汽冷凝水、压滤水、废自来水、母液水的回收和综合利用的情况。工艺改进后,青岛海晶化工集团有限公司12万t/a PVC装置可节水67万t/a,节约资金204万元/a。     

Contributions to characterization of poly(vinyl chloride)–lignin blends

The present study evaluates the impact of blending organosolv and kraft lignins, which are natural polymer by‐products in the pulp and paper industry, with plasticized poly(vinyl chloride) (PVC) in flooring formulations. Also examined is the impact of replacing dioctyl phthalate, a PVC industry general‐purpose plasticizer, with diethylene glycol dibenzoate (Benzoflex 2‐45), tricresyl phosphate (Lindol), or alkyl sulfonic phenyl ester (Mesamoll) in these formulations. The influence of the different types of lignins and plasticizers on the processibility, thermal, and mechanical properties of the blends is discussed. These properties demonstrate that partial replacement of PVC (20 parts) with different lignins is feasible for some formulations that can be successfully used as matrices for a high level of calcium carbonate filler in flooring products. In addition, the data demonstrate that the presence of certain plasticizers, which interfere with the intramolecular interactions existing in lignins, may allow the lignin molecules to have more molecular mobility. The morphology and the properties of PVC plasticized lignin blends are strongly influenced by the degree and mode of the lignin plasticization and its dispersion within the PVC matrix. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2732–2748, 2006     

以氧化镁和氧化锌为主稳定剂的PVC的热稳定性和力学性能

用HAAKE流变仪研究了氧化镁／氧化锌稳定体系对聚氯乙烯的动态热稳定性能。结果发现，在氧化镁／氧化锌质量比为2／3的条件下，配合环氧大豆油、硬脂酸钙、无毒亚磷酸酯和有机稳定剂作为辅助稳定剂，其初期着色和热稳定效果都超过了市售钙锌稳定体系，流变性能和动态热稳定特性接近铅盐稳定体系。用这种稳定体系稳定的PVC的力学性能与市售钙锌稳定体系稳定的相当。     

废紫铜催化制备氯化亚铜新工艺

介绍以废紫铜为原料，在催化剂作用下，铜直接同盐酸，空气中氧发生反应制备氯化亚铜的新工艺，试验确定了最佳反应条件，产品质量达到了GB1619－79的标准要求，该工艺具有原料消耗少，反应速度快，流程短，操作简单，生成成本低等特点。     

3,5-二氯苯甲酸的合成

考察了在以邻氨基苯甲酸为原料，三氯化铁为催化剂，X为溶剂，直接通氯氯化，再经重氮化合物3，5－二氯苯甲酸的工艺过程中，物料配比，反应湿度等反应条件对收率的影响，确定了合成的适宜条件，通过此合成工艺，产品的收率可达85％以上。     

柱前衍生反相高效液相色谱法快速测定3,5-二氯苯甲酰氯

以无水甲醇作柱前衍生试剂，建立了反相高效液相色谱法间接测定3，5-二氯苯甲酰氯的新方法。实验结果表明，在流动相：甲醇-水（85：15），流速：1．0mL／min，检测波长：288nm的条件下，定量校正曲线具有良好的线性关系，相关系数（r）为0．9999。方法用于样品中标题物质的测定，RSD=0．19％（n=6），加标回收率为99．9％-105％。     

十六烷基三甲基溴化铵活化催化合成香豆素

以无水碳酸钾为催化剂、十六烷基三甲基溴化铵(HTMAB)为活化剂，用水杨醛和醋酸酐为原料通过Perkin反应合成香豆素，研究了物料比、催化剂用量和HTMAB用量和反应近结束时保温时间对产率的影响。结果表明：用HTMAB为活化剂，可有效活化碱催化剂无水碳酸钾，提高了其碱性，与无HTMAB时相比，香豆素产率有较大提高，其最佳反应条件是n(水杨醛)：n(乙酸酐)：n(碳酸钾)：n（HTMAB)为1．00：3．00：0．25：0．03，反应温度185℃，反应近结束时保温3h，香豆素产率可达85．3％。     

Electrochemistry at capped platinum nanoparticle Langmuir Blodgett films: A study of the influence of platinum amount and of number of LB layers

Platinum nanoparticles (n-Pt), over-grafted with 2-thiophenecarbonyl chloride are assembled on gold electrodes, by the Langmuir Blodgett (LB) technique using behenic acid (BHA) as promoting agent. These layers are electrochemically active without any preliminary activation. The [Fe(CN)₆]^3−/4− redox couple was used as electrochemical probe. This paper reports on the influence of the number of deposited LB layers, and the n-Pt density on the electrochemical response. n-Pt density was modified by the change of the “BHA/n-Pt” ratio. Cyclic voltammograms of “[Fe(CN)₆]^3−/4−” were observed whatever the coating conditions. As soon as the first layer was deposited the electrochemical response was associated to the n-Pt coverage, its response slightly increased up to a steady state for five or seven layers. As expected, the increase of the Pt density favored the increase of the current density. XPS analysis performed before and after electrochemical cycling showed that 4-mercaptoaniline capped platinum nanoparticles, and their over grafting were chemically and electrochemically stable. Analysis of influence of the number or the n-Pt density of the layers showed that the electrochemically active part of LB electrodes was provided by the last layer plus a part of the underlying one.