光引发丙烯酰胺沉淀聚合研究

以丙酮/水为溶剂，采用紫外光（UV）引发丙烯酰胺（AM）沉淀聚合，考察了聚合反应的特征以及溶剂、初始单体浓度、引发剂浓度、表面入射光强、液层厚度等参数对聚合物分子量的影响。结果表明，紫外光引发丙烯酰胺沉淀聚合过程中单体转化率和聚合物分子量都随反应时间的延长而增加，光照80min时，单体转化率可达90％以上。所得聚合物分子量为10⁵～10⁶，提高单体浓度可使聚合物分子量增加，增加引发剂浓度和提高光强导致聚合物分子量降低，液层厚度对聚合物的分子量影响不大。所得聚合物粒子粒径约为200～300nm左右，粒径分布较为均匀，溶剂组成对聚合物粒子相貌影响较大，增加水含量可使粒子粒经变大但分散性变差。     

Rhythmic pattern formations in gels and Matalon—Packter law: A fresh perspective

The periodic precipitation pattern formation in gelatinous media is interpreted as a moving boundary problem. The time law, spacing law and width law are revisited on the basis of the new scenario. The explicit dependence of the geometric structure on the initial concentrations of the reactants is derived. Matalon—Packter law, which relates the spacing coefficient with the initial concentrations is reformulated removing many ambiguities and impractical parameters. Experimental results are discussed to establish the significance of moving boundary concept in the diffusion controlled pattern forming systems     

表面活性剂对均相沉淀法制备单晶Ce2O(CO3)2￠H2O微粉形貌及 形成机理的影响

在尿素及硝酸铈的混合溶液中分别加入表面活性剂CTAB、 PEG19000、OP-10,利用均相沉淀法合成了不同形貌的CeO2超细前驱体Ce2O(COa)2·H2O,采用X射线衍射及透射电子显微镜等测试手段,对产品的物相和形貌进行了表征．实验结果表明,所得产品均为斜方晶系的单晶Ce2O(CO3)2·H2O,且表面活性剂的加入使晶体的晶化程度明显提高;添加不同的表面活性剂得到不同形貌尺寸的产物: 阳离子型表面活性剂CTAB对Ce2O(CO3)2·H2O晶体的形貌影响不大,所得产物尺寸变小,且分散性得到一定的改善;非离子型表面活性剂对所得产物的形貌影响显著．加入PEG19000和OP-10分别得到了形状排列有序的、尺寸较均匀的、较规则无团聚的微米棒及具有紧密结合中心的发散状的花样微粒．不同形貌前驱体的形成与晶粒形成生长机理的改变有关．     

纳米氧化锌粉的表面改性研究

以Zn(NO3)2·6H2O和CO(NH2)2为原料,采用均相沉淀法制备纳米氧化锌粉.用扫描电镜对产物粒度大小、形貌进行观察,并对其影响因素进行了探讨.结果表明,在反应温度为120℃,反应时间为2.5h时,所制的纳米氧化锌的产率最大.用不同的表面改性剂对纳米ZnO进行表面改性,粉体不再发生团聚.图6,表7,参5.     

泡沫分离,带溶剂萃取和沉淀法提取庆大霉素

研究了用文题法从水相中分离砂大霉素的各种操作因素对分离过程的影响。在最适条件下，种方法对庆大霉素配制液的收率分别为７２％，８８％，８７％，无机盐能使沉淀收率提高。将上述３法用于发酵液时，泡沫法和萃取法的收率均有显著降低，而沉淀法依然能达到很高的收率，ψ＝捍沉淀率约为１００％．     

从芒果皮中提取果胶的工艺研究

果胶是一种大分子多糖类物质 ,具有良好的胶凝作用 ,用途广泛 ,在国内外市场上的销量很好。 1 990年世界上果胶总产量约 2 5 0 0 0吨 ,而我国 1 990年仅在食品工业上消耗的果胶就达 1 0 0 0吨 ,但国内市场上销售的果胶大部分为进口货[1] 。果胶在我国的生产仍处于开发阶段 ,所以发掘新的提取资源、提高果胶质量、降低果胶生产成本的意义十分重大。目前 ,已有以柑桔皮、向日葵盘、苹果皮、香蕉皮、马铃薯渣为原料提取果胶的研究报道 ,如何从芒果皮中提取果胶却未见报道。芒果在制造罐头和饮料中副产大量下脚料———芒果皮 ,未能得到充分利用…     

Indirect automatic atomic absorption determination of sulphate based on its precipitation with barium

A continuous precipitation flame atomization atomic absorption spectrometric method for the indirect determination of sulphate is proposed. By using a reversed flow-injection configuration for precipitation as barium sulphate, this anion was determined in the range 10–150 g/ml, with a relative standard deviation of 2.6%. The sensitivity was increased by a factor of seven by using a nitrous oxide-acetylene flame to measure barium.     

Genetic engineering to enhance the selectivity of protein separations

The ability to recover and purify natural and recombinant proteins, and the costs of doing so remain a major task in introducing the potential products of biotechnology. The bases for separation range from specific binding onto tailored reagents to solubility and partitioning behavior governed by a mixed bag of size, charge, and hydrophobicity. In most cases, a combination of methods is used in sequence, and improvements in the selectivity at an early stage can enhance the effectiveness of subsequent (and usually more costly) steps. Genetic engineering provides a means of improving the selectivity within the context of existing separation methods. By this strategy, improvements in selectivity are sought by bestowing a distinctive property on the protein of interest. The primary sequence of amino acids is altered, such that the protein can be selectively removed from other components of the multicomponent mixture in which such products are commonly found. In this article, the range of these “distinctive properties” and their pairing with various separation methods will be reviewed. Specific examples from our work, in which a distinctive charge is provided via a polypeptide “purification” fusion tail, will be discussed. Separation methods we have used with these fusion proteins are precipitation, two-phase aqueous extraction, reversed micellar extraction, and ion exchange using both resins and membranes.     

碳酸氢铵沉淀法制备氧化钇粉体时反应条件对产物粒度的影响

研究了碳酸氢铵沉淀法的反应条件对氧化钇粒度的影响,探讨了粒度变化规律。发现在沉淀反应中,晶型碳酸钇铵的形成与否是影响氧化钇粒度的关键因素。在较低的反应温度下,当碳酸氢铵和氯化钇的浓度大于0.25mol·L-1,摩尔比大于5,陈化时间大于60min时得到碳酸钇铵沉淀,经煅烧可获得粒度(D50)大于1μm的氧化钇。当反应物浓度较低、摩尔比小,陈化时间较短时得到无定型碳酸钇沉淀,煅烧沉淀可获得粒度(D50)小于0.5μm的氧化钇。实验证明选择适当的沉淀反应条件,可制备D50在0.3～10μm范围内的不同粒度级别的氧化钇粉体。     

琼脂凝胶中形成铬酸铅周期性沉淀的机理研究

选择硝酸铅和铬酸钾作为相互扩散的反应物以形成铬酸铅在琼脂凝胶中的周期性沉淀．分别在光照和黑暗中对六种不同浓度的硝酸铅溶液进行了实验．根据实验现象对周期性沉淀的形成提出了可能的机理．认为光辐射可使铬酸铅部分电离，从而减慢了胶核成长速率，有利于汇聚成带．