水中总氮的测定预处理方法改进

采用COD消解管和COD消解仪代替标准方法中具塞比色管和高压灭菌器进行消解，调整了取样体积，减少了碱性过硫酸钾加入量和其中氢氧化钠的用量.试验结果表明，改进预处理方法后绘制的标准曲线，相关系数为0.999 5，检出限为0.05 mg/L，相对标准偏差小于5%，样品加标回收率为98.0%~102%.与标准方法相比，改进后的方法精密度和准确度都有一定的提高，并且分析时间缩短，过程得到简化.改进后的方法和标准方法进行t检验比较无明显差异，可满足水中总氮的快速、准确测定.     

NH_2基态和激发态的SAC－CI和量子拓扑方法研究

ＮＨ_２基态和激发态的ＳＡＣ－ＣＩ和量子拓扑方法研究郑世钧，蔡新华，宋天乐，孟令鹏，中迁博，波田雅彦（河北师范学院化学系，石家庄，０５００９１）（京都大学工程学院京都，日本）关键词ＳＡＣ－ＣＩ方法，激发态，电子密度，拓扑分析用量子拓扑学方法研究激发态...     

重力场热力学分析和重力化学势

用分析比较的方法对重力场热力学作了新思考，建立了重力场中的Ｇｉｂｂｓ方程和重力化学势，使处理方法简单通用，与普通热力学方法衔接起来，应用大为方便。     

含RGD序列环肽以及类似物的合成方法研究

通过文献检索，总结了含RGD序列环肽以及类似物的合成方法，该类化合物的 合成方法较多，生物活性较好，值得继续研究。     

蔗糖水解实验数据处理与误差分析

为了提高蔗糖水解反应实验结果准确性，采用误差分析的方法，对不同数据处理方法进行分析，提出了一个准确、快速，适于学生实验的数据处理方法：采用外推法确定α0，进而计算α∞；采用二次曲线拟合ln（α—α∞）与时间关系，计算速率常数。该方法的分析结果能够反映实验过程中温度对速率常数的影响。     

检测水中汞离子的化学试剂及其制备方法

检测水中汞离子的化学试剂及其制备方法，涉及一种化学试剂，尤其是涉及一种高选择性的、能够定性、半定量及定量检测水中汞离子的化学试剂及其制备方法。提供高选择性的、能够定性、半定量及定量检测水中汞离子的化学试剂及其制备方法。其合成方法为：先合成罗丹明酰肼，在容器中加入罗丹明染料，以有机溶剂溶解，再加入水合肼，     

漆原钴法制备四羰基钴钠及羰基化反应

谈基钻的传统制备方法“提在高温高压下，由合成气与钻盐反应制备出CO。（CO）s，再经某些化学处理方法制备Na［CO（CO）。I，但其反应条件苛刻，操作手续繁杂，成本高，不利于大量推广应用．制备四谈基钻盐方法，还有KCN转化法［”，NaBH。还原法‘’‘等，但各种方法均有一定缺点．我们报道了Ranev－Ni催化剂催化合成Na［Co（CO）。」的新方法＊”‘．此方法收率高，反应条件温和，具有较好的应用前景，但仍存在Ni、CO分离的问题．进一步改进催化剂、降低成本、高效地合成N迁C。（CO）。」仍是解决问题的关键．为此，我们探讨…     

微波消解电感耦合等离子体发射光谱法测定塑料中铅和镉

采用微波消解技术溶样，ICP-AES法测定了塑料中的铅和镉。通过对消解试剂和微波温度程序的研究，建立了塑料样品的微波消解方法。该方法与传统马弗炉高温灰化消解方法比较，具有准确、简便、快速、省试剂、污染少、消解完全等优点。方法回收率为93％～106％，相对标准偏差(n=7)均小于2％。实际样品对比分析结果表明，方法具有良好的准确度，适于多种塑料材料中铅和镉的快速分析。     

分析方法的认证

一个方法在应用到分析实际试样之前，必须经过严格的认证，以确认分析方法在准确度、精密度、适用的浓度范围以及抗干扰能力等方面是否能够达到试样对分析方法的要求．另一方面，即使是可靠的方法，例如法定的分析方法，当一个实验室或个人初次使用时，也要通过认证，以证明在当时的条件下方法能被正确地执行．     

固相萃取-气相色谱-串联质谱法检测水中18种酚类化合物

当前水中酚类化合物种类不清、危害不明，多种酚类化合物的同时检测方法不成熟，因此建立水中多种酚类化合物同时检测的方法具有重要现实意义。该研究建立了固相萃取结合气相色谱-串联质谱同时检测水中18种酚类化合物的分析方法。实验选择超纯水为空白样品，采用固相萃取技术富集、提取水中的酚类化合物，同时对水样初始pH值、洗脱液的种类、洗脱液的用量等条件进行优化，从而确定出最优的前处理方法，最后利用气相色谱-串联质谱法对不同种类的酚类化合物同时进行定量检测。实验结果表明，在初始水样pH值为3.0、不衍生等条件下，使用10 mL乙酸乙酯洗脱，控制洗脱速度为1 mL/min，经固相柱富集净化，氮吹浓缩后，用气相色谱-质谱仪（EI源）测定，选择离子模式监测，外标法定量。结果表明，以3倍信噪比结合浓度外推法确定方法检出限，为0.04~0.6 μg/L；18种酚类化合物的加标回收率为51.7%~117.3%，相对标准偏差为3.1%~7.4%。应用建立的方法分别检测了河流湖泊水、生活用水、生产用水3大类6种不同的水质。检测结果表明，河流湖泊水中酚类化合物所含种类最多，含量最高。研究建立的方法不需要衍生，简化了前处理方法，操作简单，且准确性高，重复性好，可同时检测复杂水体中多种酚类化合物，能显著提高酚类化合物的分析速率。该方法的建立对我国水中酚类化合物残留水平的控制、检测标准的制定和管理措施的采取，都具有重要的理论和现实意义。     

Sixteen capillary electrophoresis applications for viral vaccine analysis

A broad range of CE applications from our organization is reviewed to give a flavor of the use of CE within the field of vaccine analyses. Applicability of CE for viral vaccine characterization, and release and stability testing of seasonal influenza virosomal vaccines, universal subunit influenza vaccines, Sabin inactivated polio vaccines (sIPV), and adenovirus vector vaccines were demonstrated. Diverse CZE, CE-SDS, CGE, and cIEF methods were developed, validated, and applied for virus, protein, posttranslational modifications, DNA, and excipient concentration determinations, as well as for the integrity and composition verifications, and identity testing (e.g., CZE for intact virus particles, CE-SDS application for hemagglutinin quantification and influenza strain identification, chloride or bromide determination in process samples). Results were supported by other methods such as RP-HPLC, dynamic light scattering (DLS), and zeta potential measurements. Overall, 16 CE methods are presented that were developed and applied, comprising six adenovirus methods, five viral protein methods, and methods for antibodies determination of glycans, host cell-DNA, excipient chloride, and process impurity bromide. These methods were applied to support in-process control, release, stability, process- and product characterization and development, and critical reagent testing. Thirteen methods were validated. Intact virus particles were analyzed at concentrations as low as 0.8 pmol/L. Overall, CE took viral vaccine testing beyond what was previously possible, improved process and product understanding, and, in total, safety, efficacy, and quality.     

Spectrophotometric and fluorimetric determination of diazepam, bromazepam and clonazepam in pharmaceutical and urine samples

New spectrophotometric and fluorimetric methods have been developed to determine diazepam, bromazepam and clonazepam (1,4-benzodiazepines) in pure forms, pharmaceutical preparations and biological fluid. The new methods are based on measuring absorption or emission spectra in methanolic potassium hydroxide solution. Fluorimetric methods have proved selective with low detection limits, whereas photometric methods showed relatively high detection limits. Successive applications of developed methods for drugs determination in pharmaceutical preparations and urine samples were performed. Photometric methods gave linear calibration graphs in the ranges of 2.85-28.5, 0.316-3.16, and 0.316-3.16 microgml-1 with detection limits of 1.27, 0.08 and 0.13 microgml-1 for diazepam, bromazepam and clonazepam, respectively. Corresponding average errors of 2.60, 5.26 and 3.93 and relative standard deviations (R.S.D.s) of 2.79, 2.12 and 2.83, respectively, were obtained. Fluorimetric methods gave linear calibration graphs in the ranges of 0.03-0.34, 0.03-0.32 and 0.03-0.38 microgml-1 with detection limits of 7.13, 5.67 and 16.47 ngml-1 for diazepam, bromazepam and clonazepam, respectively. Corresponding average errors of 0.29, 4.33 and 5.42 and R.S.D.s of 1.27, 1.96 and 1.14 were obtained, respectively. Statistical Students t-test and F-test have been used and satisfactory results were obtained.     

Effect of certain chemical compounds on secondary metabolites of Penicillium janthinellum and P. duclauxii

The secondary metabolites of Penicillium janthinellum and P. duclauxii were affected by different concentrations of cadmium nitrate, sodium chloride, and sucrose. The fungal culture characteristics including mycelial fresh and dry weight, colony diameter, colony spore mass and reverse color, number of spores, and secondary metabolites were affected as well. Cyclopenin, carlosic acid, erythroskyrin, kojic acid, and patulin were produced by P. janthinellum on cadmium nitrate-free medium. However, cyclopenin, carlosic acid, frequentin, and islandicin were produced at 100 ppm, and cyclopenin at 500 ppm. On the other hand, the secondary metabolites produced by P. duclauxii were 9 on cadmium nitrate-free medium, 7 on medium containing 100 and 500 ppm of cadmium nitrate, and 4 at 1000 ppm cadmium nitrate concentration. Secondary metabolite brevianamide A was produced in the presence and absence of cadmium nitrate. The duclauxin, patulin, terrestic acid, and xanthomegin were produced only on cadmium nitrate-free medium. However, mycophenolic acid was produced only on cadmium nitrate-containing medium. The kojic acid was produced by P. janthinellum at 0.0%, 0.5%, 1.0%, 2.0%, 3.0%, and 5.0% concentrations of sodium chloride. The carlosic acid, erythroskyrin, and patulin were produced only at 0.0% and 1.0%. While carolic acid and islandicin were produced at 1%, 2%, and 3% and frequentin was produced only at 2% and 3%. On the other hand, 8 secondary metabolites were produced by P. duclauxii at 0.0%, 0.5%, 1.0%, and 2.0% concentration of sodium chloride and only 4 were produced at 3%. The secondary metabolites produced by P. janthinellum were 7 at 10% and 20%, 6 at 30%, and 2 only at 40% concentrations of sucrose. However, 8 secondary metabolites were produced by P. duclauxii at 10%, 20%, 30% and 3 at 40% concentrations of sucrose.     

The Book Corner

Abstract

Liquid Chromatography/Mass Spectrometry, Techniques and Applications, A. L. Yergey, C. G. Edmonds, I. A. S. Lewis, and M. L. Vestal, Modern Analytical Chemistry Series, D. Hercules, Editor, 306 pages, Plenum Press, New York and London, 1989. $65.00; price 20% higher outside USA and Canada.

Analytical Microbiology Methods, Chromatography and Mass Spectrometry, A. Fox, S. L. Morgan, L. Larsson and G. Odham, Editors, Plenum Press, New York and London, 1920, 280 pages. $65.00; prices 20% higher outside USA and Canada.

Ion Chromatography, H. Small, Modern Analytical Chemistry Series, D. Hercules, Editor, Plenum Press, New York and London, 1990, 376 pages. $49.50; prices 20% higher outside USA and Canada.     

3D printing to innovate biopolymer materials for demanding applications: A review

Biopolymers are widely available, low-/nontoxic, biodegradable, biocompatible, chemically versatile, and inherently functional, making them highly potential for a broad range of applications such as biomedicine, food, textile, and cosmetics. 3D printing (3DP) is capable of fabricating some customized, complex material structures composed of single or multiple material constituents that cannot be achieved by conventional methodologies (e.g. internal structures design); thus, 3DP can greatly expand the application of biopolymer materials. This review presents a comprehensive survey of the latest literature in 3DP technology for materials from biopolymers such as polysaccharides and proteins. The most commonly used 3DP techniques (i.e. inkjet printing, extrusion-based printing, stereolithography, selective laser sintering, and binder jetting) in biomedical and food fields are discussed. Critical factors affecting the quality and accuracy of 3D-printed constructs, including rheological characteristics, printing parameters (e.g. printing rate, and nozzle diameter, movement rate, and height), and post-printing processes (e.g. baking, drying, and crosslinking) are analyzed. The properties and the emerging applications of 3D-printed biopolymer materials in biomedical, food, and even wider applications (e.g. wastewater treatment and sensing) are summarized and evaluated. Finally, challenges and future perspectives are discussed. This review can provide insights into the development of new biopolymer-based inks and new biopolymer-based 3D-printed materials with enhanced properties and functionality.     

Stress-induced increase in the amounts of maysin and maysin derivatives in world premium natural compounds from centipedegrass

The red leaves of centipedegrass are known to produce compounds with stronger antibiotic effects than those produced by green leaves. Therefore, the aim of this study was to identify if stress methods (e.g., gamma irradiation, UV-B irradiation, and wounding) could effectively convert green leaves to red leaves, and thereby increase the production of maysin and maysin derivatives that have been known for antibiotic properties. Our results showed differential concentration changes for different compounds using these stress methods. The concentrations of luteolin increased from 0.014% to 0.019%, 0.022%, and 0.028% following gamma irradiation, UV-B irradiation, and wounding, respectively. The concentration of isoorientin increased from 0.898% to 1.938% and 2.538%, while the concentration of mixed rhamnosylisoorientin and orientin increased from 0.303% to 0.474% and 0.690%, following UV-B irradiation and wounding, respectively. Gamma irradiation produced concentrations of isoorientin, rhamnosylisoorientin, and orientin similar to those found in red leaves. The concentrations of derhamnosylmaysin increased from 0.004% to 0.009%, 0.015%, and 0.024% by gamma irradiation, UV-B irradiation, and wounding, respectively. The concentration of maysin increased from 0.515% to 0.714%, 0.583%, and 0.777% by gamma irradiation, UV-B irradiation, and wounding, respectively, while the concentration of luteolin-6-C-boivinopyranoside increased from 0.324% to 0.834%, 0.979%, and 1.493% by gamma irradiation, UV-B irradiation, and wounding, respectively. According to these results, wounding and gamma irradiation are promising methods for increasing the concentrations of maysin and maysin derivatives.     

Polymer-surfactant and protein-surfactant interactions

The phase behavior and some physicochemical properties of homopolymers (HP) and hydrophobically modified (HMP) polymers, as well as of polyelectrolytes (PE) and proteins (PR), in the presence of aqueous surfactants, or their mixtures, are discussed. Mixing the above components gives rise to the formation of organized phases, whose properties are controlled by polymer and/or surfactant content, temperature, pH, and ionic strength. Depending on the nature, concentration, and net charge of both solutes, molecular solutions, polymer-surfactant complexes, adsorption onto micelles and vesicles, gels, liquid crystalline phases, and precipitates are observed. Such rich polymorphic behavior is the result of a complex balance between electrostatic, excluded volume, van der Waals, and other contributions to overall system stability. It is also modulated by the molecular details and architecture of both the polymer and the surfactant. Different experimental methods allow investigation of the above systems and getting information on the nature of polymer-surfactant interactions (PSI). Surface adsorption and thermodynamic methods, together with investigation of the phase diagrams, give information on the forces controlling PSI and on the existence of different phases. Conductivity, QELS and viscosity allow estimating the size and shape of polymer-surfactant (protein-surfactant) complexes. Optical microscopy, cryo-TEM, AFM, NMR, fluorescence, and relaxation methods give more information on the above systems. Use of the above mixtures in controlling gelation, surface covering, preparing dielectric layers, and drug release is suggested.     

含希夫碱侧基聚酯及其锌配合物的合成和性能

经多步反应合成2种新型含希夫碱侧基聚酯(P5,P6),进一步与醋酸锌反应得到2种聚酯锌配合物(P5-Zn,P6-Zn)。 采用元素分析、FT-IR、UV-Vis、¹H NMR、GPC、TG、DSC和荧光光谱等技术手段对其结构和性能进行表征。 P5和P6均溶于四氢呋喃(THF)、氯仿(CHCl₃)、N,N-二甲基甲酰胺(DMF)、N,N-二甲基乙酰胺(DMAc)、二甲基亚砜(DMSO)、N-甲基吡咯烷酮法(NMP)等有机溶剂,P5-Zn和P6-Zn部分溶于THF及CHCl₃,溶于DMF、DMAc、DMSO、NMP等有机溶剂。 P5和P6的重均相对分子质量M_w及相对分子质量分布指数PDI分别为4164、6148 g/mol和1.42、1.43。 P5、P6、P5-Zn和P6-Zn的5%失重温度分别为339、348、367和358℃。 P5、P6、P5-Zn和P6-Zn的玻璃化转变温度T_g分别为88.8、123.3、39.8和63.8 ℃。 P5和P6的DMF溶液(5×10^-5 mol/L)在418和416 nm处发射弱紫色荧光,P5-Zn和P6-Zn的DMF溶液(5×10^-5 mol/L)在505和506 nm处发射强绿色荧光,固体P5-Zn和P6-Zn在527和532 nm处发射强绿色荧光。     

Determination of carbohydrates and sweeteners in foods and biologically active additives by high-performance liquid chromatography

A method for the determination of large amounts of carbohydrates (glucose, lactose, maltose, mannose, sucrose, and fructose) and sweeteners (xylitol and sorbitol) by reversed-phase liquid chromatography with refractive index detection without derivatization has been developed. The limits of determination for glucose, fructose, and sucrose in liquid samples were 0.1 g/L, and for xylite, lactose, maltose, mannose, and sorbite, 1 g/L. In solid samples the limits of determination for glucose, fructose, and sucrose were 0.1%, and for xylite, lactose, maltose, mannose, and sorbite, 0.6%. The method is applicable to the analysis of samples of wine, juice, honey, cookies, dairy products, and biologically active additives. The developed method for the determination of carbohydrates and sweeteners in foods and biologically active additives was certified in the Mendeleev Institute for Metrology (St. Petersburg).     

Analysis of selected phytotoxins and mycotoxins in environmental samples

Natural toxins such as phytotoxins and mycotoxins have been studied in food and feed for decades, but little attention has yet been paid to their occurrence in the environment. Because of increasing awareness of the presence and potential relevance of micropollutants in the environment, phytotoxins and mycotoxins should be considered and investigated as part of the chemical cocktail in natural samples. Here, we compile chemical analytical methods to determine important phytotoxins (i.e. phenolic acids, quinones, benzoxazinones, terpenoids, glycoalkaloids, glucosinolates, isothiocyanates, phytosterols, flavonoids, coumestans, lignans, and chalcones) and mycotoxins (i.e. resorcyclic acid lactones, trichothecenes, fumonisins, and aflatoxins) in environmentally relevant matrices such as surface water, waste water-treatment plant influent and effluent, soil, sediment, manure, and sewage sludge. The main problems encountered in many of the reviewed methods were the frequent unavailability of suitable internal standards (especially isotope-labelled analogues) and often absent or fragmentary method optimization and validation.