微波消解- 火焰原子吸收光谱法测定蜂胶中金属元素含量

目的:测定一种原产地为加拿大的蜂胶中金属元素的含量,为进一步研究蜂胶营养价值提供数据,同时改进测量方法。方法:用微波消解法处理样品,用硝酸和过氧化氢的混合物作为消解剂进行微波消解,并优化消解条件,然后用火焰原子吸收光谱法测定蜂胶制品中钙、铁、镁、锌、钠、钾、铜的含量。结果:七种元素相对标准偏差为0.85%~2.33%(n=7),回收率在96.5%~104.7%之间。试验结果表明该蜂胶中含有丰富的金属元素,且与河南产蜂胶相比,加拿大产蜂胶中多种金属元素含量远低于河南产蜂胶。结论:使用本文方法测定蜂胶中的金属元素含量,结果准确,方法可靠。为进一步探讨蜂胶制品金属元素与其保健功能的关系提供了有用数据。     

微波消解－火焰原子吸收光谱法测定蜂胶中金属元素含量

目的：测定一种原产地为加拿大的蜂胶中金属元素的含量,为进一步研究蜂胶营养价值提供数据,同时改进测量方法。方法：用微波消解法处理样品,用硝酸和过氧化氢的混合物作为消解剂进行微波消解,并优化消解条件,然后用火焰原子吸收光谱法测定蜂胶制品中钙、铁、镁、锌、钠、钾、铜的含量。结果：七种元素相对标准偏差为O．85％～2．33％（n=7）,回收率在96．5％～104．7％之间。试验结果表明该蜂胶中含有丰富的金属元素,且与河南产蜂胶相比,加拿大产蜂胶中多种金属元素含量远低于河南产蜂胶。结论：使用本文方法测定蜂胶中的金属元素含量,结果准确,方法可靠。为进一步探讨蜂胶制品金属元素与其保健功能的关系提供了有用数据。     

微波消解-FAAS法测定普通甘薯和紫甘薯中的金属元素

采用微波消解法处理普通甘薯和紫甘薯样品,运用火焰原子吸收光谱法测定其中的K、Ca、Mg、Fe、Mn、Zn、Cu 7种对人体有益的金属元素含量。结果表明,普通甘薯和紫甘薯中K、Ca、Fe、Mg元素含量较高,Mn、Zn、Cu元素含量较低,且7种金属元素含量在两者之间存在一定的差异,各元素在紫甘薯中的含量均比普通甘薯中含量高。方法的加标回收率介于98.5%～103.2%,相对标准偏差(RSD)不大于3.14%。可为普通甘薯与紫甘薯的品质评价提供理论参考。     

利用原子吸收光谱法和电镜能谱仪法分析重金属Pb、Cd在水稻颖果不同部位中的分配

比较研究了传统原子吸收光谱法与电镜能谱仪法分析重金属Pb、Cd在水稻籽粒不同部位中的分配情况,研究结果表明:两种方法均显示,Pb、Cd在水稻颖果中的分配为胚>糊粉层>果皮>近糊粉层处胚乳>颖果中心,其中,胚、糊粉层和果皮Pb、Cd含量差异较小,整个胚乳Pb、Cd含量变化也不大,但胚、糊粉层和果皮Pb、Cd含量显著高于胚乳.扫描能谱仪能够准确反映重金属在植物不同部位分布的差异,结果与原子吸收光谱法无显著差异.扫描能谱仪法的优点在于操作方便快捷,但是只能用于定性,不能定量测定出某一部位重金属的准确含量,因此,不能代替传统的原子吸收光谱法.     

微波消解-FAAS法分析并比较旱芹(Apium graveolens L.)不同部位八种金属元素的含量

采用微波消解法处理旱芹根、茎、叶,并用火焰原子吸收法测定其中的Na、K、Ca、Mg、Fe、Mn、Zn、Cu 8种金属元素的含量。结果表明:旱芹中富含人体必需的Na、K、Mg、Fe、Ca等元素,各元素在不同部位含量有一定差异。Fe元素在旱芹根中含量为883.57μg.g-1,明显高于茎和叶;Ca、Zn和Mn元素在旱芹叶中的含量分别为11 103.74,214.04,88.07μg.g-1,明显高于茎和根;K、Na和Mg元素在旱芹茎中的含量高于根和叶中,Cu元素含量在各部位差异不大。方法的加标回收率为96.8%～105.8%,相对标准偏差(RSD)≤3.36%。     

黔西南红土型金矿硬叶小金发藓对几种金属元素的吸收、富集特征

利用原子吸收法测定黔西南红土型金矿硬叶小金发藓(Pogonmon neesii(C.Muell)Dozy)植株及其土壤中的Au、Pb、Cu、、Zn、Ca、Mg、Hg和As等8种金属元素含量,并分析它们之间的相关性及植物对金属的富集能力.结果表明:硬叶小金发藓体内的金属元素含量普遍较高,对不同金属元素的吸收、富集具有较大的差异,Ca-Mg呈极显著正相关,Cu-Zn、Hg-As呈显著正相关.该植物对Hg和As均具有强烈的富集作用.     

深圳福田红树植物群落特征及金属元素分布状况

通过对深圳福田红树林群落特征的研究,对红树植物的区系组成、群落的外貌和结构、群落的主要类型和分布进行了概述,并对该红树林中的桐花树+秋茄+白骨壤+老鼠簕+海漆混交群落林地土壤和红树植物的金属元素分布进行分析。结果发现,该林地土壤金属元素含量分布具有一定规律性,元素K、Na、Ca、Mg在各层土壤中分布均匀;必需金属元素Fe、Mn在各层土壤中含量变化不明显;非必需重金属元素Cr、Ni、Pb、Hg、Cd和必需元素Zn、Cu含量从底层至表层逐步提高;金属元素在该林地红树植物中分布也具有一定规律性,元素K、Na、Ca、Mg在五种红树植物的不同部位均大量存在;必需金属元素Fe、Mn、Zn、Cu在各种红树植物中含量FeMnZnCu;非必需重金属元素Cr、Ni、Pb、Hg、Cd在各种红树植物中含量表现出差异性,秋茄和海漆中Ni含量较大,白骨壤中Pb含量最大,桐花树中Cr含量最大,老鼠簕Cu含量最大,Cd和Hg在五种红树植物中含量都最低;植物中金属元素含量分布和土壤中金属元素含量分布具有相关性。     

黑果枸杞中十三种元素含量的测定

采用原子吸收法测定了黑果枸杞中钙、镁、铜、锌、锰、铁、铅、镍、镉、钴、铬、钾、钠等元素的含量 ,为对其深入研究提供了科学资料。结果表明 :黑果枸杞中钙、镁、铜、锌、铁等元素的含量远高于宁夏枸杞中相应各元素的平均含量 ,钾、锰含量远低于其平均值 ,钠含量与其相当。钴含量远高于绿叶蔬菜的含量 ,铬含量较牛奶中含量低。镍含量比谷物、腌肉、蔬菜中的高。镉、铅含量较普通植物中的略低 ,不构成污染。     

四种金花茶组植物叶片金属元素含量及富集特性研究

以四种金花茶组植物为研究对象,采用原子吸收光谱法和原子荧光法,测定其嫩叶、老叶及对应土壤中Mg、Ca、Mn、Fe、Zn、Ni、Se、Pb、Cd、Hg、As共11种元素的含量,并分别计算嫩叶和老叶对土壤金属元素的富集系数.结果表明:(1)4种金花茶组植物叶片富含Mg、Ga、Mn、Fe、Zn、Ni等营养元素,各元素在叶片中含量为Ca>Mg>Mn>Fe>Zn>Ni>Se;Pb、Cd、As、Hg等重金属元素含量较低,均达到无公害茶叶标准.(2)老叶和嫩叶中各金属元素含量差异较大,老叶中的Ca、Mn、Fe、Zn、Pb、Cd、Hg、As、Se元素含量均大于嫩叶,尤以Ca、Mn、Fe差异显著;嫩叶中的Mg和Ni含量大于老叶.(3)金花茶组植物对不同金属元素的富集能力不同,对各元素富集能力强弱为Ca、Mn、Mg>Zn、Ni、Hg>Pb、Se>Fe、As,老叶和嫩叶的富集规律存在差异.(4)不同金花茶组植物对金属元素的富集能力有较大差异,龙州金花茶(Camellia longzhouensis)和黄花抱茎茶(C.murauchii)对Mg、Ca、Mn、Zn、Ni、Se、Pb的富集能力均大于金花茶(C.nitidissima)和毛籽金花茶(C.ptilosperma).其中,龙州金花茶对Mg、Mn、Se的富集能力最强,黄花抱茎茶对Ca、Pb、Hg富集能力最强,金花茶对Hg的富集能力较强,对其它元素的富集能力均较弱;毛籽金花茶对Ca、Mn、Ni、Zn的富集能力均最弱.该研究结果为金花茶组植物的进一步开发和利用提供了理论依据.     

满江红金属元素含量的种间差异及其富集特性研究

为揭示满江红属(Azolla Lam.)植物资源材料对金属元素吸收积累特性差异,该研究采用ICP-MS的方法,对8种21个满江红品系的12种金属元素含量进行测定分析,比较不同种类满江红中金属元素含量的差异及富集特性,通过主成分分析确定满江红属品系的特征金属,并采用聚类法对供试材料进行分类。结果表明:(1)满江红属植物中金属元素含量变异系数大于30%的有8种,其中Mo含量在品系间差异最大(127.73%),Ca含量在品系间差异最小(18.94%)。(2)满江红属植物对土壤中不同金属元素的富集能力不同,富集系数大小依次为Mn>Mg>Mo>K>Cd>Ca>1。(3)不同种满江红对金属元素K、Mg、Mn、Zn、Mo的富集能力存在显著差异(P<0.05)。(4)满江红的特征金属元素为Cd、Hg、Ca、Mn、Cu、Zn、K和Cr。(5)基于特征金属元素含量的聚类结果显示,当遗传距离为15时,可将21份满江红资源分为3类,与传统分类基本吻合,其中品系‘3006’和‘MH3-1’对重金属Cd、Cr和Hg的富集能力较强,聚为一类。研究认为,满江红对金属元素的富集存在种间差异,且这种差异可以作为满江红品种分类的参考依据。     

猕猴自然感染肝片吸虫诱发胆管结石的形成

在研究肝片吸虫诱发猕猴自发性胆结石形成的病理学基础上,采用红外光谱分析、原子吸收光谱分析和组织化学染色对胆结石的成分及结构进行了测定,初步探讨了本病发生的机理。在一只９岁雌性猃猴肝总胆管内发现４条肝片吸虫（Ｆａｓｃｉｏｌａ ｈｅｐａｔｉｃａ）,胆囊胆汁中检出大量肝片吸虫虫卵。左侧胆管内有一颗棕黑色结石,直径为１ｃｍ、长约２．５ｃｍ圆柱形。肝细胞灶性坏死伴有轻度结缔组织增生,胆管腺体重度增生,上皮细     

Instrumental analysis of microbiologically influenced corrosion

Appropriate application of techniques for detection andmonitoring of microbiologically influenced corrosion isessential for understanding the mechanistic nature of theinteractions and for obtaining control methods. This paperreviews techniques and methods applied tomicrobiologically influenced corrosion in recent years.The techniques presented in this paper includeelectrochemical noise measurement, concentric electrodes,scanning vibrating electrode mapping, electrochemicalimpedance spectroscopy, atomic force microscopy,confocal laser microscopy, Fourier transform infraredspectroscopy, x-ray photoelectron spectroscopy, Augerelectron spectroscopy, extended x-ray absorption finestructure and utilization of piezoelectric materials. Thesetechniques are reviewed regarding the heterogeneouscharacteristics of microbial consortia and their possibleinfluences on metal substrata. We hope this review willmotivate application and combination of new techniquesfor practical detection and on-line monitoring of theimpact of biofilms on engineering alloys.     

The measurement of multiple spray deposits by sequential application of metal chelate tracers

Chelates of the transition metals copper, cobalt, manganese and zinc, available as foliar feeds, were identified as the most suitable spray tracers for comparisons of deposits arising from up to four sequential applications to a single target. Their use minimised many of the disadvantages associated with other commonly used tracers such as visible and fluorescent dyes, and it was possible to quantify each tracer when present on the target in ratios of up to 100:1. Each spray solution contained a single chelate at a metal concentration of 1 g litre^?1. The recovery of metal chelates from plant tissue may not be quantitative, as a consequence of absorption or adsorption by leaves for example. The food colorant tartrazine, at a concentration of 10 g litre^?1, was shown to be a suitable internal standard for estimation of percentage recovery. Combined spray deposits were recovered readily from apple leaves and fruit by aqueous extraction and analysed by atomic absorption spectroscopy. The spray deposit of each metal tracer was calculated from the raw analytical data using procedures for generating calibration curves designed to optimise the accuracy of the analysis.     

Definitive Structural Identification toward Molecule‐Type Sites within 1D and 2D Carbon‐Based Catalysts

Developing facile preparation routes and atomic‐level characterization methods for single‐atom catalysts is highly desirable but still challenging. Herein, a general strategy is proposed to construct transition metal single atoms within 1D and 2D carbon supports. The carbon supports, typically graphene and carbon nanotubes, are coated with various transition metal‐containing bimetal hydroxides, followed by polydopamine coating and high‐temperature pyrolysis. X‐ray absorption fine structure spectroscopy measurements and simulations efficiently indicate that single atoms (Co, Fe, or Cu) are captured within the applied carbon supports, distinctively forming exclusive molecule‐type sites. As a proof‐of‐concept application, the obtained catalysts exhibit remarkable performance for electrochemical oxygen reduction reaction, even surpassing commercial Pt/C catalyst. The developed versatile route opens up new avenues for the design of carbon‐based catalysts with definite molecular active sites. The atomic‐level structural identifications provide significant guidance for mechanistic studies toward single‐atom catalysts.     

Physical and chemical characterization of soil and poultry litter humic and fulvic metal complexes

Summary Humic and fulvic-zinc complexes obtained from soil and poultry litter were characterized by I.R. spectroscopy, determination of stability constant and the free energy change associated with their formation. Infrared spectroscopy confirmed that both electrovalent, coordinate-covalent bonds of Zn²⁺ with the carboxylate, phenolic hydroxyl and amine groups lead to the formation of their stable complexes. This is evident from the changes in absorption bands at 1700 cm^–1, 1725 cm^–1, 1625 cm^–1 and 1400 cm^–1 of their infrared spectra.The stability constants of complexes are pH-dependent. Interaction of Zn with humic and fulvic acid involved the formation of mononuclear complexes. The values of stability constants of these complexes are lower than those reported earlier.The calculation of the free-energy change associated with salts and complex formation indicates the spontaneity of both reactions, although a higher probability of complex reaction than that of salt formation is evident. The implications of the complexation of metal ions by these naturally occurring polydisperse plyaanions in regulating the movement of metal ions from the ambient soil matrix to plant roots and biological system in terresterial and aquatic environments are indicated.Journal paper no. 2, Department of Soil Science and Agricultural Chemistry, Rajendra Agricultural University, Tirhut College of Agriculture, Dholi, Muzaffarpur, Bihar, India.     

Preparation and Optical Characterization of Core–Shell Bimetal Nanoparticles

Chemical approaches allow for the synthesis of highly defined metal heteronanostructures, such as core–shell nanospheres. Because the material in the metal nanoparticles determines the plasmon resonance-induced absorption band, control of particle composition results in control of the position of the absorption band. Metal deposition on gold or silver nanoparticles yielded core–shell particles with modified optical properties. UV–vis spectroscopy on solution-grown, as well as surface-grown, particles was conducted and provided ensemble measurements in solution. Increasing the layers of a second metal leads to a shift in the absorption band. A shell diameter comparable to the original particle diameter leads to a predominant influence by the shell material. Extent of shell growth could be controlled by reaction time or the concentration of metal salt or reducing agent. Besides optical characterization, the utilization of atomic force microscopy, scanning electron microscopy, and transmission electron microscopy yielded important information about the ultrastructure of nanoparticle complexes. Surface-grown core–shell particles were superior in terms of achievable shell thickness, because of difficulties encountered with solution-grown particles due to salt-induced aggregation.     

Unraveling the Rapid Redox Behavior of Li‐Excess 3d‐Transition Metal Oxides for High Rate Capability

Li‐excess 3d‐transition metal layered oxides are promising candidates in high‐energy‐density cathode materials for improving the mileage of electric vehicles. However, their low rate capability has hindered their practical application. The lack of understanding about the redox reactions and migration behavior at high C‐rates make it difficult to design Li‐excess materials with high rate capability. In this study, the characteristics of the atomic behavior that is predominant at fast charge/discharge are investigated by comparing cation‐ordered and cation‐disordered materials using X‐ray absorption spectroscopy (XAS). The difference in the atomic arrangement determines the dominance of the transition metal/oxygen redox reaction and the variations in transition metal–oxygen hybridization. In‐depth electrochemical analysis is combined with operando XAS analysis to reveal electronically and structurally preferred atomic behavior when a redox reaction occurs between oxygen and each transition metal under fast charge/discharge conditions. This provides a fundamental insight into the improvement of rate capability. Furthermore, this work provides guidance for identifying high‐energy‐density materials with complex structural properties.     

Self-assembly of a peptide sequence,EKKE, composed of exclusively charged amino acids: Role of charge in morphology and lead binding

The self-assembly of peptides is influenced by their amino acid sequence and other factors including pH, charge, temperature, and solvent. Herein, we explore whether a four-residue sequence, EKKE, consisting of exclusively charged amino acids shows the propensity to form self-assembled ordered nanostructures and whether the overall charge plays any role in morphological and functional properties. From a combination of experimental data provided by Thioflavin T fluorescence, Congo red absorbance, circular dichroism spectroscopy, dynamic light scattering, field emission-scanning electron microscopy, atomic force microscopy, and confocal microscopy, it is clear that the all-polar peptide and charged EKKE sequence shows a pH-dependent tendency to form amyloid-like structures, and the self-assembled entities under acidic, basic and neutral conditions exhibit morphological variation. Additionally, the ability of the self-assembled amyloid nanostructures to bind to the toxic metal, lead (Pb²⁺), was demonstrated from the analysis of the ultraviolet absorbance and X-ray photoelectron spectroscopy data. The modulation at the sequence level for the amyloid-forming EKKE scaffold can further extend its potential role not only in the remediation of other toxic metals but also towards biomedical applications.     

Nickel localization on tissues of hyperaccumulator species of Phyllanthus L. (euphorbiaceae) from Ultramafic Areas of Cuba

Two species of perennial Phyllanthus (Euphorbiaceae) (Phyllanthus orbicularis and Phyllanthus discolor, both endemic to ultramafic areas of Cuba, and their natural hybrid, Phyllanthus xpallidus) were selected for metal localization microanalysis. Different plant tissues were analyzed by X-ray fluorescence, inductively coupled plasma—atomic emission spectroscopy, and scanning electron microscopy coupled with an energy-dispersive X-ray probe. All of the studied taxa are nickel (Ni) hyperaccumulators and significant concentrations of this element were found in different leaf and stem tissues. The highest Ni content was found in the laticifer tubes, whereas leaf epidermis Ni content resulted to be much more relevant in terms of total metal storage. Calcium and magnesium were found more evenly distributed in leaf and stem tissues.