三氟氯氰菊酯农药中微量杂质的液相色谱－质谱法鉴定

用高效液相色谱－质谱联用技术研究了三氟氯氰菊酯农药的杂质及含量,并用源内碰撞诱导解离（CID）技术鉴别了所存在的微量杂质。方法实用性强,色谱分离效果好,可用于该农药各成分的定性、定量分析。     

SPME/GC-MS鉴别地沟油新方法(Ⅱ)

采用固相微萃取/气相色谱-质谱(SPME/GC-MS)方法测定地沟油中的微量杂质成分,通过对各种纯正植物油中的内源性微量成分与不同地区地沟油中的外源性杂质成分的对比分析,以及对地沟油中杂质成分来源的分析,确定了广州、贵州、深圳、北京等地区地沟油的特征成分,并作为鉴别指示成分。该方法灵敏度高、特征性强,在卫生部组织的地沟油检测盲样考核中,对阳性样品判断的准确率高达95.5%。     

赛默飞发布环境水样中的碘、硫氰酸和高氯酸的检测方案

<正>赛默飞世尔科技(以下简称赛默飞)不久前发布了基于Thermo ScientificTM Q ExactiveTM Focus组合型四极杆Orbitrap质谱仪的药物杂质分析解决方案,帮助用户快速高效地采集隐藏在大量母药中微量杂质的质谱信息,并对其进行有效的鉴定和定量分析。     

高纯氧化钨中微量杂质的ICP—MS法测定

报道了高纯氧化钨中铅，等微量杂质的电感耦合等离子体质谱测定方法。连择了仪器最佳操作参数，考察了质谱干扰和基体效应，选用标准加入法可克服基体效应。方法不经分离富集，各元素测量值与标准值相吻合，相对误差小于５％，方法快速，准确。     

A Novel Method for the Identification of Gutter Oils Using SPME/GC - MS ( Ⅱ )

采用固相微萃取/气相色谱-质谱(SPME/GC- MS)方法测定地沟油中的微量杂质成分,通过对各种纯正植物油中的内源性微量成分与不同地区地沟油中的外源性杂质成分的对比分析,以及对地沟油中杂质成分来源的分析,确定了广州、贵州、深圳、北京等地区地沟油的特征成分,并作为鉴别指示成分.该方法灵敏度高、特征性强,在卫生部组织的地沟油检测盲样考核中,对阳性样品判断的准确率高达95.5％.     

松毛虫性信息素微量成分鉴定方法的研究

采用气相色谱-质谱分析确认了顺-5-,反-7-十二碳二烯乙酸酯是思茅松毛虫性信息素腺体的主要成分（次要成分由于含量极微且受杂质干扰,未能获得全扫描质谱图）。利用高分辨率毛细管气相色谱分析了思茅松毛虫性信息素腺体提取物的酯基转移和乙酰化反应的衍生物,进一步确认了顺-5-,反-7-十二碳二烯醇是思茅松毛虫性信息素腺体中的微量成分。探讨了功能团相互转换微量化学反应法鉴定松毛虫性信息素腺体中微量成分功能团和立体构型的优点。强调了性信息素微量成分鉴定工作在昆虫化学通讯系统研究中的重要性。     

程序涂渍气相色谱柱的应用——微量有机物的定量分析

关于程序涂渍气相色谱柱理论研究已做了一系列的工作,其应用也已经引起了色谱工作者的关注。由于程序涂渍色谱柱具有分析速度快、分离效能高的特点,很适合于有机物中微量杂质的测定,尤其微量杂质在主组分之后出峰的情况下更能显示出程序柱的优越性。     

二环己胺中微量苯胺等杂质的气相色谱与气-质联用分析

二环己胺可由苯胺催化加氢制得,故产物中有苯胺等杂质存在。苯胺等杂质对二环己胺产品质量有严重的影响,因此二环己胺纯度需达到99．5％以上,苯胺的含量应低于0．1％。本文以苯甲醇为内标,建立了二环己胺产品中微量苯胺的气相色谱分析条件,并且采用气相色谱一质谱(GCMS)分析了各杂质峰的归属,发现二环己胺产品纯度达不到     

DEIP中微量杂质的GC/MS分析

研究了间苯二甲酸二乙酯(DEIP)中微量杂质的化学成分,用减压精馏的方法对样品进行分离浓缩,用气相色谱-质谱法(GC/MS)进行分析,结合生产工艺,谱库检索及人工解谱进行鉴定,鉴定出DEIP中主要11种杂质,用归一化法进行定量,建立了用GC/MS方法检测DEIP中微量杂质的方法。     

天然维生素E制品中杂质的分离与鉴定

利用高效液相色谱、气相色谱-质谱联用与高分辨质谱对天然维生素E制品中的杂质进行了分离分析与结构鉴定。采用正相高效液相色谱法分离天然维生素E的4种异构体及2种杂质,并对杂质馏分进行富集纯化。将气相色谱-质谱联用与高分辨质谱检测相结合,用于获得杂质的结构信息。通过比较杂质精确相对分子质量和解析质谱碎片离子,推断杂质为芝麻素及其同分异构体表芝麻素。经与芝麻素对照品保留时间及碎片离子数据比对,确证了对杂质结构的推断。所建立的杂质鉴定方法快捷、有效,可应用于天然维生素E制品的食品安全控制。     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

PHONONS IN POLYACENIC CHAINS

We have theoretically resolved phonon excitations in quasi-two-dimensional organic crystals of polyacenic semiconductor material which may be obtained by the pyrolytic treatment of phenol-formaldehyde resin. A model for studying the dynamical properties using three polyacene chains is proposed with the aim to present the vibrational properties of this structure. It employs the formalism of solid states in two dimensions which admit phonons. A simulation process of the two-dimensional lattice structure shows that elastic waves may explain the existence of vibrational modes in the frequency range 100-400 cm-1. The presence of acoustic and optical like phonons is discussed in terms of the elastic force constants. A hyperfine resonance structure is obtained. It allows the analysis of the dynamical evolution in thin films of polyacene. It is found that the behavior of the phonon density of states exhibits resonance between modes in the structure.     

液晶聚合物/柔性链聚合物共混体系相分离形态

利用元胞动力学方法在二维情况下对浓度、取向序参量的含时Ginzberg-Landau方程进行数值求解,研究了液晶聚合物/柔性链聚合物共混体系的相分离动力学,考察了浓度、取向有序过程的耦合对相分离形态的影响.结果表明,此耦合作用对相分离的时间进程以及相分离图样的空间排布都有影响.液晶聚合物的取向有序相当于增加了两组分间的不相容性而促进两相分离;两个序参量在热力学方面的耦合使液晶聚合物趋向于沿着界面方向取向,而动力学方面的耦合使液晶聚合物分子沿着其取向方向扩散,相分离图样的空间排布由这两种效应共同决定通过极化率张量的定义用数值方法模拟得到了相分离体系的小角光散射图样,结果表明,散射强度分布具有方位角依赖性,它是由浓度、取向序参量的空间变化共同决定的.     

Investigations of the Mechanism of Alternating Copolymerization with Charge-Transfer Interaction of the Monomers

The applicability of the method of Giese to the measurement of the influence of monomer reactivity is examined. The reaction of alkyl mercuric salts with sodium borohydride permits the production of alkyl (cyclohexyl and butyl) radicals. Since hydrogen radicals are present in high concentration, the addition of alkenes to the reaction mixture leads to radicals from the alkenes. Further addition of alkene (polymerization) can be nearly completely excluded in this way. The composition of the reaction products is determined by gas chromatography. The addition rate of the alkenes relative to styrene allows correlation with the e value of the Q-e scheme of Alfrey and Price. The method answers the question of how far addition of the monomer complex occurs in one step or as separate addition of both monomers during copolymerization in the presence of charge-transfer (CT) complexes of the monomers. The investigations are performed by using the styrene/acrylonitrile/ZnCl₂system, and it is demonstrated that the reactivity of the complexed     

Contributions to the Chemistry of the Binary Compounds of the Transition Elements

Phase and structural relationships of the sulfur, selenium, and tellurium compounds of the 4d and 5d transition elements of groups IV to VII of the periodic system are discussed. Homologous elements behave very similarly with respect to the chalcogens, and this is particularly the case for niobium and tantalum, and for molybdenum and tungsten. However, zirconium, niobium, and molybdenum have a greater tendency towards formation of chalcogen-poor phases than their homologues hafnium, tantalum, and tungsten. Subchalcogenides are known only for zirconium and niobium. The number of phases and the tendency towards formation of solid solutions are considerably smaller among the tellurides than among the sulfides and selenides. The crystal structures of the telluride phases also differ from those of the sulfide and selenide phases of analogous composition. In addition, a review of the phase and structural relationships of the arsenic and antimony compounds of the 4d and 5d transition elements of groups V to VII is given.     

电流变液中悬浮颗粒的体积与形状的变化

基于偶极近似,运用电极化方法,定量研究了电流变液中悬浮颗粒在外电场作用下其体积和形状的变化,并计算了其体积和形状的相对变化率.研究结果表明:悬浮颗粒的体积和形状的相对变化率均与电场强度的平方成正比,并与ER本身的性质有关.一般情况下,颗粒的体积和形状的相对变化率分别为8.4%和12.5%,对总体积变化率的贡献为1.68%.这种变化对于ER系统的电涨和电热都作出了贡献,仅当将颗粒当作刚性球时,其自由能才与电场强度的平方成正比.     

A NOVEL APPROACH TO RHEOLOGICAL CHARACTERIZATION FOR THE GELATION IN POLYMER CRYSTALLIZATION

The isothermal crystallizations of three kinds of commercial isotactic polypropylene have been studied by DSC and rheometric experiments, in a range of temperatures where the rate of crystallization is moderate. As the crystallization proceeds, volume contraction induces tensile force upon the parallel plates. The tensile force relaxed quickly in liquid states,but after a critical amount of the relative crystallinity, it starts to accumulate in the static test, that is, with the motionless parallel plates. A new method to determine the liquid-solid transition by the static tensile force is proposed and compared with two dynamic methods of detecting liquid-solid transition, that is, the power-law modulus theory and the yield modulus model. The tensile force method predicted considerably earlier transition than the dynamic methods, and the corresponding DSC data indicate relative crystallinity of larger than 0.2 at the transition times. The limitation of dynamic methods and other possible errors have been analyzed. While the dynamic methods are suitable for slow crystallization, the tensile force method is more appropriate for the crystallization of moderate rates. Moreover, it has the advantage of almost not disturbing the crystallizing materials before the transition.     

Dielectric analysis of PMMA microcapsules containing an aqueous KCl solution to derive a distribution function of the release rate of KCl

Release of KCl from a batch of PMMA microcapsules containing an aqueous 3 mM KCl solution was studied with the following two methods: 1) dielectric measurements of suspensions of the microcapsules in distilled water. The electrical conductivity of capsule interior was estimated with this method. 2) Measurements of the conductivity of suspending medium of the microcapsule suspensions. These two kinds of experiments provided us with information about the amount of KCl remaining in the capsules and that diffused outside. Results of these experiments showed that the microcapsules varied in their release rate of KCl. A distribution function of the release rates was derived from the results of the dielectric measurements. That distribution function was successful in explaining the results of the measurements of the conductivity of suspending medium. Furrther examination revealed that the release rate increased with the increase in the thickness of capsule wall.     

Thermoelectric Properties of Czochralski GeSi Crystal

In order to discuss the application possibility of SiGe crystal in thermoelectric materials,we investigated the thermoelectric properties of several silicon-germanium alloys with different content,orientation and electric conductive type. As discussed in the experiment result,the absolute value of Seebeck coefficient fluctuates from 300 to 600 μV/K in the whole temperature range. In the present paper,the relationship of Seebeck coefficient against content,orientation and electric conductive type is summarized in detail. The Seebeck coefficient of the sample with <111> orientation is smaller than that in <100> at the same temperature. Absolute value of P-type is larger than that of N-type except pure Ge. But as the temperature increases,the absolute value of pure Ge decreases many times as quickly as that of other specimens. In addition,the specimens of bulk GeSi alloy crystals for experiment were grown by the Czochralski method through varying the pulling rate during the growing process.     

Chain dynamic parameters for some acrylic polymers

The dielectric relaxation data of Ishida et al. on a number of acrylic polymers are represented in terms of the relaxation function proposed by Havriliak and Negami using the multi-response techniques developed by Havriliak and Watts. Two of the parameters of this function are interpreted in terms of a temperature dependent distribution of relaxation times. In this method of interpretation the breadth of the distribution function is temperature-dependent while the skewness is not. The temperature dependence of the breadth of the distribution function is similar for most of these acrylic polymers.The parameters of the relaxation function are also interpreted in terms of Mansfield's model which represents intra- and inter-molecular interactions in terms of springs and dash pots. Briefly, increasing the side chain length for the methacrylate series increases the inter-molecular relaxation time which may be due to an increase in the entropy of activation for the orientation process. The difference between the one acrylate in this study and the four methacrylates of the series is a reduction in the intra-molecular relaxation time, apparently due to the lack of the alpha methyl group.