应用FTIR-XRD-XRF分析测试技术研究新型仿制绿松石的矿物学特征   总被引：4，自引：3，他引：1  

严俊  刘晓波  王巨安  方飚  刘培钧  杨彬彬 《岩矿测试》2015,34(5):544-549

近年来绿松石及其仿制品的鉴定工作较多局限于应用傅里叶变换红外光谱对仿制品进行简单的筛选,前人报道的仿制绿松石的矿物组成主要为单一的矿物相(如异极矿、三水铝石、磷铝石、羟硅硼钙石、菱镁矿等)。本文应用傅里叶变换红外光谱(FTIR)、X射线粉晶衍射(XRD)与X射线荧光光谱(XRF)对当前珠宝市场上几种新型仿制绿松石进行了初步分类,并对不同类别的仿制绿松石的具体矿物组成、物相及晶型特征作了对比研究。结果表明,这些新型仿制绿松石可分为三大类:一类主要由硅酸盐(斜硅钙石)与碳酸盐(方解石)两种矿物组成;另一类为白云石与方解石两种碳酸盐矿物的混合相;第三类以硅酸盐类为主要矿物,并含有钡长石、辉石与石英。显然,新型仿制绿松石的矿物组成明显相异于传统仿制品,可见仿制绿松石的矿物组成日趋多样性、复杂化,该现状必然对新型仿制样品的物相鉴定提出了更高的要求。  相似文献   

基于FTIR和MODIS数据估算新疆沙漠宽波段地表比辐射率     

李火青  吴新萍  买买提艾力&#  买买提依明  霍文  杨兴华  杨帆  何清  刘永强 《中国沙漠》2017,37(3):523-529

基于FTIR和MODIS数据,建立了新疆沙漠宽波段（8～13.5 μm）地表比辐射率的最优估算模型。首先,利用傅立叶变换热红外光谱仪观测的塔克拉玛干沙漠地表比辐射率光谱数据,结合同期MODIS温度/比辐射率产品MOD11A1的29、31和32波段比辐射率值和MOD09A1的第7波段反射率值,建立宽波段地表比辐射率估算模型,并分别采用观测数据和光谱库数据验证了模型的精度,估算结果的均方根误差分别为0.0041和0.0081。其次,选择最优估算模型,利用MODIS数据,估算了新疆4个沙漠的宽波段地表比辐射率,得到了沙漠地表比辐射率的空间分布特征。结果表明：塔克拉玛干沙漠和库鲁克库姆沙漠气候干燥稳定,地表比辐射率分布较为均匀,范围为0.850～0.915;古尔班通古特沙漠受到植被和地表水分的影响,比辐射率空间分布不均匀,范围为0.890～0.915;库木塔格沙漠的地表比辐射率分布与其羽状地表类似,范围为0.860～0.910。  相似文献   

Chemical and spectroscopic characterization of dissolved humic substances in a mangrove-fringed estuary in the eastern coast of Hainan Island, China   总被引：1，自引：0，他引：1  

张耀玲  杜金洲  彭浡  张芬芬  赵欣  张经 《中国海洋湖沼学报》2013,31(2):454-463

Mangrove-derived dissolved organic matter(DOM) has an important effect on estuarine and coastal area on a large scale.In order to improve the understanding of origin,composition,and fate of DOM in mangrove-fringed estuarine and coastal areas,dissolved humic substances(DHS) were isolated from one mangrove pore-water sample and one near-shore seawater sample downstream the mangrove pore-water site in the eastern coast of Hainan Island,South China.Fulvic acids,humic acids and XAD-4 fractions were obtained from the two water samples by using a two-column array of XAD-8 and XAD-4 resins.Chemical and spectroscopic methods were used to analyze the features of these DHS.Compared to the mangrove pore-water DHS,the near-shore seawater DHS were found rich in 13 C with lower C/N ratios and more aliphatic compounds and carbohydrates,but less aromatic structures and carboxyl groups.As for the three fractions of the two DHS,XAD-4 fractions contain more aliphatics,carbohydrates,carboxyl groups,and enrich in 13 C with respect to both fulvic and humic acids.Photo-oxidation transformation and contribution from marine-derived DOM were considered as the main reasons resulted in the difference in compositional features for these DHS in this study.  相似文献   

Study of the Interaction Mechanism in the Biosorption of Copper(II) Ions onto Posidonia oceanica and Peat     

Marta Izquierdo  Paula Marzal  Carmen Gabaldón  Margherita Silvetti  Paola Castaldi 《洁净——土壤、空气、水》2012,40(4):428-437

A systematic approach was used to characterize the biosorption of copper(II) onto two biosorbents, Posidonia oceanica and peat, focusing on the interaction mechanisms, the copper(II) sorption–desorption process and the thermal behavior of the biosorbents. Sorption isotherms at pH 4–6 were obtained and the experimental data were fitted to the Langmuir model with a maximum uptake (q_max) at pH 6 of 85.78 and 49.69 mg g^?1, for P. oceanica and peat, respectively. A sequential desorption (SD) with water, Ca(NO₃)₂, and EDTA was applied to copper‐saturated biosorbents. Around 65–70% copper(II) were desorbed with EDTA, indicating that this heavy metal was strongly bound. The reversibility of copper(II) sorption was obtained by desorption with HCl and SD. Fourier transform IR spectroscopy (FTIR) analysis detected the presence of peaks associated with OH groups in aromatic and aliphatic structures, CH, CH₂, and CH₃ in aliphatic structures, COO^? and COOH groups and unsaturated aromatic structures on the surface of both biosorbents, as well as peaks corresponding to Si? O groups on the surface of peat. The results of SEM‐EDX and FTIR analysis of copper‐saturated samples demonstrated that ion exchange was one of the mechanisms involved in copper(II) retention. Thermal analysis of biosorbent samples showed that copper(II) sorption–desorption processes affected the thermal stability of the biosorbents.  相似文献   

Effects of mechanical and chemical processes on the degradation of plastic beach debris on the island of Kauai, Hawaii   总被引：3，自引：0，他引：3  

David A Cooper  Patricia L Corcoran 《Marine pollution bulletin》2010,60(5):650-654

Plastic debris is accumulating on the beaches of Kauai at an alarming rate, averaging 484 pieces/day in one locality. Particles sampled were analyzed to determine the effects of mechanical and chemical processes on the breakdown of polymers in a subtropical setting. Scanning electron microscopy (SEM) indicates that plastic surfaces contain fractures, horizontal notches, flakes, pits, grooves, and vermiculate textures. The mechanically produced textures provide ideal loci for chemical weathering to occur which further weakens the polymer surface leading to embrittlement. Fourier transform infrared spectroscopy (FTIR) results show that some particles have highly oxidized surfaces as indicated by intense peaks in the lower wavenumber region of the spectra. Our textural analyses suggest that polyethylene has the potential to degrade more readily than polypropylene. Further evaluation of plastic degradation in the natural environment may lead to a shift away from the production and use of plastic materials with longer residence times.  相似文献   

墨绿色仿翡翠品的宝石学特征     

李锐  ;徐志  ;熊燕  ;张佩文  ;张跃峰 《地质科学译丛》2014,(5):49-54

我国玉器市场的繁荣发展,使得玉器优劣并存,导致大量墨绿色“石材”充斥市场,充当翡翠销售.在广东玉器加工批发集散市场上收集了多种墨绿色仿翡翠原料,挑选具有代表性的4件原料进行测试分析.通过宝石显微镜观察、折射率、密度以及红外光谱、X射线粉末衍射、偏光显微镜薄片鉴定等测试方法进行对比研究.该4件样品的密度、折射率与翡翠一致,红外反射光谱与绿辉石非常相似,但其结构特征、矿物组成明显区别于翡翠.综合国标判定,该4件样品均为仿翡翠品.笔者提醒,常规宝石学测试和红外光谱测试不易区分此类制品,而加强基础性研究、提高镜下鉴定能力是防范检测风险的有效途径.  相似文献   

Ground-based FTIR Measurements with High Temporal Resolution     

W. Bell  C. Paton Walsh  P.T. Woods  T.D. Gardiner  M.P. Chipperfield  A.M. Lee 《Journal of Atmospheric Chemistry》1998,30(1):131-140

We outline how ground-based Fourier transform infrared (FTIR) measurements of stratospheric trace species, obtained with high temporal resolution, could be used to detect filaments of polar vortex air at mid-latitudes and therefore test high spatial resolution chemical transport models (CTMs). Vertical column abundances of HCl, ClONO2, HNO3, N2O and HF have been obtained from FTIR solar absorption measurements made throughout the day from Aberdeen, UK (57°N, 2°W) on several days during winter/spring 1993/94 and 1994/95. The short-timescale ( 2 hours) variability observed in the columns is attributed to real atmospheric variations and is often associated with the passage of high latitude air over Aberdeen. This is confirmed by 3D modelling studies which qualitatively reproduce and rationalise the observed changes in the column data on January 19 1994, January 20 1995 and February 26 1995. We describe the viewing geometry of ground-based FTIR measurements and we suggest a measurement strategy which should maximise the information retrieved on horizontal gradients in stratospheric trace species columns from FTIR measurements.  相似文献   

傅立叶变换红外光谱联用技术在化石燃料分析中的应用   总被引：2，自引：0，他引：2  

高志农  牛菲 《岩矿测试》1998,17(1):58-63

对傅立叶变换红外光谱联用技术在化石燃料分析中的应用进行了较全面的总结评述,重点介绍了气相色谱／红外光谱联机、高压液相色谱／红外光谱联机、薄层色谱／红外光谱联机、超临界流体色谱／红外光谱联机、裂解色谱／红外光谱联机、热重分析／红外光谱联机、气相色谱／红外光谱／质谱三机联用技术等在化石燃料的结构组分分析、成因机理研究及其勘探等诸方面的重要应用,尤其是在芳香族化合物和几何异构体的分离鉴定方面发挥出的突出功效。引用文献５９篇。  相似文献   

巴西绿欧泊的宝石学特征     

钟倩  亓利剑  邵慧娟  周彦 《地质科学译丛》2013,(4):29-36,91

近期国内珠宝市场上出现一种产自巴西的绿欧泊,该类绿欧泊表现出的宝石矿物学特征与传统的欧泊有着明显差异。采用常规宝石学测试手段,并结合电子探针、X射线粉末衍射、扫描电子显微镜、红外吸收光谱、紫外吸收光谱等测试分析方法,就其化学成分、物相、微结构、谱学特征及颜色成因等问题展开初步研究。结果表明,巴西绿欧泊的主要矿物组成为蛋白石,含不等量的α-方石英和α-鳞石英等次要矿物,整体呈不规则胶柬状结构,局部微波纹理发育;该类欧泊主要由直径约10～30nm的SiO2球粒聚集而成;由H2O和M—OH倍频振动致近红外吸收谱带位于7000cm-1处,由H2O合频振动致近红外吸收谱带分别位于5200,5612cm叫处,由M—OH与[SiO4]合频振动致近红外吸收谱带位于4600-4100cm-1范围内。笔者还对巴西绿欧泊的呈色机理一并给予了探讨。  相似文献   

具磷灰石假象绿松石的岩石矿物学及谱学特征     

申广耀  卢保奇  亓利剑 《上海国土资源》2013,(4):96-100

采用x射线粉晶衍射（XRD）、博里叶变换红外光谱（FTI码以及拉曼光谱等方法对安徽马鞍山具磷灰石假象的绿松石进行了研究。结果表明：其主要矿物组成为绿松石,保留了磷灰石六边形的形态特征。XRD~U试的特征谱线d值为36745～36748（111）、29008～29025（123）、34247～34293（2101、32709～32781（113）、61626～61781（011）3020130～20162（301）,与绿松石的标准衍射谱线基本致。红外光谱测试分析表明：3510～3465cm。间的谱带归属绿松石0（OH）的伸缩振动,3300～3070cm’间的谱带归属为绿松Nu（M-H。O）伸缩振动,1210-1012cm’间的谱带归属为绿松石U3口O。）ira缩振动,在838cm。附近的吸收谱带归属为绿松石6（OH）弯曲振动,655-480cm。间的谱带归属为绿松石u4（P04）弯曲振动。拉曼光谱测试分析表明：3466cm’附近的尖锐拉曼谱峰归属于绿松石（OH）基团的伸缩振动所致,宽缓的拉曼谱峰3281cm’~03078cm’归属于绿松石中水合络离子的伸缩振动,798cm’谱峰则是由于OH的弯曲振动所致。  相似文献