应用彩色红外航空像片进行城市居民生活条件调查和分析

本文介绍了应用彩红外航片对城市居民生活条件进行调查和分析,其基本方法是:首先通过直接和间接判读标志,对居民物质生活条件和精神生活条件进行解译,然后从方便度和舒适度两项评价指标入手,选取八项评价因子,进行定量的综合评价和空间分析,最后提出改善实验区居民生活条件的建议。     

热红外测量海表面温度中的ε修正

提出了一种简单的用红外辐射计获得海表面温度的方法。该方法应用了一个快速、均匀搅拌的水浴与一支精密的水银温度计，获取海表面温度的反演系数(又称等效比辐射率)，避开了海水辐射率、大气温度和红外辐射计的响应函数等问题。在未知辐射率、大气温度、响应函数的情况下，仍可得到高于0.2℃的精度。     

Characterization of minerals and organic phosphorus species in marine sediments using soft X-ray fluorescence spectromicroscopy

Phosphorus Near Edge X-ray Fluorescence Spectroscopy (P-NEXFS) data were collected on phosphorus containing phases including organic and inorganic compounds and minerals. Although phases containing P in the plus five oxidation state P(V) in a tetrahedral PO₄ structure have similar primary fluorescence peak positions, the size, shape, and positions of secondary spectral features are diagnostic for different compounds and minerals. In particular, calcium phosphates exhibited a notable post-peak shoulder at 2154.5 eV, while oxidized iron phosphates had a distinctive pre-peak feature at 2148 eV. Polyphosphates have a broad secondary peak located approximately 2 eV higher in energy than a similar feature in phosphate esters and diesters. Compounds containing P(V) in structures other than PO₄ tetrahedra such as phosphonates have a primary peak shifted about 1 eV lower than corresponding organo-phosphates. Organo-phosphates with P in the plus three oxidation state P(III) such as phosphines had primary fluorescence peaks shifted still further down in energy (2–3 eV). The substitution of aromatic carbon groups in close proximity to P structures in organic compounds generated both pre- and post-peak features as well as a number of secondary peaks. In addition, X-ray fluorescence mapping of P, Si, Al, Mg, and Na was conducted on a marine sediment sample with sub-micron spatial resolution. Phosphorus was heterogeneously distributed in the sample and not correlated on a broad scale with any other element examined. Much of the P present in the sample was located in small, 0.6–8 μm size, P-rich domains. Several P-rich regions were examined with P-NEXFS using a focused beam with 60 nm resolution and were found to consist of either calcium phosphate or polyphosphate phases. The presence of significant polyphosphate-dominated regions in a marine sediment sample supports the recent observations that such phases can play an important role in marine P cycling. The combination of fluorescence mapping and P-NEXFS data collection on fine particles provides a powerful new tool for environmental phosphorus studies.     

Revised ab initio models for H2-H2 collision-induced absorption at low temperatures

A revised ab initio calculation of the H₂-H₂ collision-induced absorption results in significant differences compared with the work of J. Borysow et al. [Borysow, J., Trafton, L., Frommhold, L., Birnbaum, G., 1985. Astrophys. J. 296, 644-654] for wavenumbers greater than 600 cm⁻¹ and temperatures below 120 K. The revision has significant influence on the spectra of Uranus and Neptune, and essentially removes the need for models with “super-solar” helium abundances or stratospheric hazes to explain the spectrum of Uranus.     

ICP—AES光谱法测定磷矿石中多元素组分

对磷矿石中P2O5、Al2O3,caO、MgO、Fe2O3、Cd测定方法进行研究,确定试验最佳条件。元素回收率95．3％～105．4％,相对标准偏差（n=12）为2．53％-5．80％,检出限为0．5×10^-6-7．86×10^-6。经几种国家标准物质及矿石样品分析验证,结果满意。     

土体腐殖酸组分对水泥土强度影响效果试验

摘 要:工程实践发现水泥固化软土受土体腐殖酸成分的影响。当前,土体腐殖酸组分对水泥土固化影响已成为岩土工程研究的重要课题之一。通过在实际工程采样对水泥加固土腐殖酸组分进行定性、定量对比试验分析,以研究不同水泥掺量、不同地域水泥固化土腐殖酸组分的影响效果。试验结果表明:由红外光谱（IR）试验表现在水泥环境中胡敏酸组分的羧基量增多,水泥土阳离子交换量（CEC）随水泥掺量增加而增大;在5%、10%、20%水泥掺入比之水泥土中,由神经网络预测模型预测结果证实,富里酸组分对水泥土无侧限抗压强度影响效果较强。水泥土腐殖酸组分可与水泥产物Ca2+、AI3+反应,在水泥土环境生成钙、铝键等复合体,它们可能影响水泥水解水化反应,削减水泥所能达到的固化效果。 关键词:腐殖酸组分;红外光谱（IR）;电子扫描显微镜（SEM）;阳离子交换量（CEC）;水泥土。     

斑岩铜矿围岩蚀变绿帘石的光谱特征——以德兴铜矿富家坞矿区为例

斑岩型矿床具有十分广泛和明显的热液蚀变带,青磐岩化通常位于中心钾化带外侧,可分为三个亚带,绿帘石是青磐岩化带最重要的蚀变矿物之一,但目前对青磐岩化带内各亚带之中的绿帘石的特征研究较为薄弱。近年来,短波红外光谱技术(SWIR)已经广泛应用于热液蚀变矿物的识别,但由于短波红外光谱通过识别特定的基团进而识别含此基团的矿物,难以识别斑岩中部分关键蚀变矿物,如钾长石、钠长石和硬石膏。X射线衍射技术(XRD)能识别大部分蚀变矿物,可对红外光谱技术在斑岩矿床中的应用进行补充。本文以江西省德兴地区富家坞矿区为研究对象,提出应用SWIR和XRD分析辅助蚀变填图。富家坞矿区发育了十分广泛的绿帘石化,根据其共生矿物组合及空间分布,划分了三种绿帘石类型。第Ⅰ类:矿物组合为绿帘石-钠长石-石英-方解石,绿帘石和钠长石以脉状形式产出于钾化花岗闪长斑岩体内,穿切钾长石斑晶;第Ⅱ类:矿物组合为绿帘石±绿泥石-石英-方解石,绿帘石和绿泥石以集合体形式交代早期岩体内黑云母、斜长石的方式产出,并保留有原生矿物晶型,伴有方解石、石英等矿物;第Ⅲ类绿帘石共生矿物主要为石英、方解石、沸石等,含少量高岭石,主要呈不规则脉状,分布于蚀变花岗闪长斑岩外侧。通过对以上三类绿帘石进行系统SWIR和XRD分析,发现类型Ⅰ绿帘石大部分表现出较大的Fe-OH吸收峰位值(Pos2252 2255),类型Ⅱ和类型Ⅲ绿帘石大部分表现为较小的Fe-OH吸收峰位值(Pos2252 2255)。XRD结果显示绿帘石晶体特征更为明显,特征衍射峰位值{■13}晶面表现出相对集中的特征,但是次峰{022}晶面表现出一定的差异性,且绿帘石{022}晶面2. 40?衍射峰半高宽(FWHM-2)与绿帘石Dep2334/Dep2252值呈现负相关的关系。故本文认为绿帘石的次峰{022}晶面2. 40?衍射峰值及其半高宽(FWHM-2)可以作为讨论斑岩矿床围岩蚀变矿物绿帘石的结晶度的主要参数。三种绿帘石结晶指数的差异可能是热液流体演化过程中温度降低和距离岩体中心的远近造成的。     

荒漠植物花棒耐盐性的傅立叶红外光谱法研究

试验以荒漠植物花棒幼苗为材料,应用傅立叶红外光谱（FTIR）法研究了NaCl胁迫下花棒叶片主要有机化合物含量和蛋白质结构的变化以及叶片K+和Na+含量。结果表明,叶片Na+、K+含量随着0~255 mM NaCl盐胁迫逐渐增强而变化,导致Na+/K+比值逐渐降低,显示出盐胁迫下花棒幼苗具有”吸钾排纳”特性。花棒幼苗再170 mM NaCl的高浓度胁迫下24 h,叶片中蛋白质、酯类和碳水化合物含量大幅度增加。花棒的蛋白质二级结构中1 665/1 638 cm-1比值的逐渐降低。揭示出花棒植株通过增强蛋白质、酯类和碳水化合物合成代谢调控能力抵御盐胁迫的损伤,而且花棒蛋白质二级结构更趋稳定,与叶片中Na+/K+比值的变化趋势显著相关。因此花棒为了适应高浓度盐胁迫,具有叶片蛋白质、酯类快速合成以及蛋白质构象更趋于稳定的积极响应。     

用红外云图估测小区域雨强及其在短时预报中的应用

在吸收国内外对卫星估测降水的经验和方法的基础上,利用深圳自动气象站网观测资料,对卫星云图资料进行分析、对比、反演,得到小区域红外云图对流云云顶亮温与降水强度的统计关系,建立了一个利用红外云图云顶亮温,结合空气水汽含量,云顶亮温的变化进行自动短量估测小区域对流云团降雨强度的方法;利用这种方法对深圳本地的短时强降雨的估测取得较好的效果。并在此基础上,运用云团移动外推的办法预测未来小区域云顶亮温的变化,     

Pressure dependence of hydroxyl solubility in coesite

 The solubility of hydroxyl in coesite was investigated in multianvil experiments performed at 1200 °C over the nominal pressure range 5–10 GPa, at an f _O2 close to the Ni-NiO buffer. The starting material for each experiment was a cylinder of pure silica glass plus talc, which dehydrates at high P and T to provide a source of water and hydrogen (plus enstatite and excess SiO₂). Fourier-transform infrared (FTIR) spectra of the recovered coesite crystals show five sharp bands at 3606, 3573, 3523, 3459, and 3299 cm⁻¹, indicative of structurally bonded hydrogen (hydroxyl). The concentration of hydrogen increases with pressure from 285 H/10⁶ Si (at 5 GPa) to 1415 H/10⁶ Si (at 10 GPa). Assuming a model of incorporation by (4H)_Si defects, the data are fit well by the equation C _OH=Af ² _H2<\INF>Oexp(−PΔV/RT), with A=4.38 H/10⁶ Si/GPa, and ΔV=20.6 × 10⁻⁶ m³ mol⁻¹. An alternative model entailing association of hydrogen with cation substitution can also be used to fit the data. These results show that the solubility of hydroxyl in coesite is approximately an order of magnitude lower than in olivines and pyroxenes, but comparable to that in pyropic garnet. However, FTIR investigations on a variety of ultrahigh pressure metamorphic rocks have failed in all cases to detect the presence of water or hydrogen in coesite, indicating either that it grew in dry environments or lost its hydrogen during partial transformation to quartz. On the other hand, micro-FTIR investigations of quartz crystals replacing coesite show that they contain varying amounts of H₂O. These results support the hypothesis that preservation of coesite is not necessarily linked to fast exhumation rates but is crucially dependent on limited fluid infiltration during exhumation. Received: 23 August 1999 / Accepted: 10 April 2000