傅立叶变换中红外漫反射光谱法定量检测褐煤的六个关键指标

采用傅立叶变换中红外漫反射光谱法同时对褐煤中的内水分、挥发分、含硫量、高位发热量、低位发热量和折合率6个指标进行了基于最小二乘法(PLS)的定量分析。结果显示,内水分、挥发分、含硫量、高位发热量、低位发热量和折合率的相对误差分别为3.4%、2.0%、4.0%、1.4%、2.5%和2.2%,得到了满意的预测结果。采用中红外光谱分析的方式实现了一种快速分析煤炭品质的新方法,为工业在线分析煤炭品质论证了可行性。     

Supergene and hypogene alteration in the dual-use kaolin-bearing coal deposit Angren, SE Uzbekistan

The Jurassic Angren coal–kaolin deposit, Uzbekistan, is one of the largest producers of coal and kaolin suitable for refractories and industrial ceramics in central Asia. The Major coal seam, attaining a thickness between 4 and 24 m, is encased by kaolin-bearing bedsets which have been derived from supergene pre- and hypogene post coal kaolinization. Joint clay-mineralogical and coal petrographic analyses formed the basis of the environment analysis of this coal–kaolin series and constrained the physico-chemical conditions existing during the Triassic through Jurassic period of time. Massive kaolin I underneath the coal seam is a typical residual kaolin or underclay with arsenic Fe-disulfides and siderite indicative of a reducing swampy depositional environment developing under moderately hot climatic conditions. Towards the top, kaolin I became reworked fluvial by processes. The Major coal seam developed in swamps interfingering with a fluvial drainage system of suspended to mixed-load deposits. The maximum temperature for the post-depositional alteration of the carbonaceous material is 70 °C. Post-coal kaolinization (kaolin II) affecting trachyandesites and trachytes is of low-temperature origin and low-sulphidation-type. The temperature of formation was well below 200 °C, deduced from the absence of dickite in the clay mineral assemblage. Basaltic dykes intersected the coal–kaolin series and account for contact metamorphic reactions in the proximal parts of the aluminum-bearing wall rocks reaching sanidinite-facies conditions with temperatures around 1000 °C.     

土壤中可挥发污染物抽气清除法的数值模拟

抽气清除法(SVE)是最常用的清除土壤非饱和区中可挥发污染物的方法之一。介绍和分析了该法的基本原理和工艺过程,建立了描述该法中气体渗流场、污染物相间交换以及污染物随气流场运移3个主要过程的物理模型。分别采用Galerkin法和Laplace变换Galerkin法推导了模拟气体渗流场和污染物随气流运移过程的有限元数值模型,编制了三维有限元程序,给出了1个典型的三维计算实例。     

气相色谱-质谱法分析香蕉叶挥发油化学成分

采用气相色谱 质谱法 (GC/MS)分析了香蕉叶中挥发油的化学成分 ,鉴定了 2 2个化合物 ,主要成分是十七烷、二十一烷、二十八烷、三十四烷、10 甲基 十九烷、3,7,11,15 四甲基十六烷、十五烷基环己烷等 ,占整个挥发性物质的 6 1.4 5% ;其次是 2 ,6 二叔丁基 4 甲基苯酚 ,占总挥发性物质的 14 .74 %。确认了C2 0 H42 同分异构体。     

The ‘orogenic andesite’ puzzle of C. E. Tilley: 1—Is the volatile phase the missing piece?

Some 65 years ago, C. E. Tilley, in his 1950 Presidential Address to the Geological Society of London, brought into sharp focus the then perhaps-not-fully-recognised problem of the origin of what he termed the ‘orogenic andesites’—and, in particular, their commonly constituent calc-alkaline lineage of lavas and pyroclastic materials. In spite of much investigation and progress since, the problem remains not fully resolved. The two most conspicuous features of such orogenic—i.e. island arc—volcanism are its copious, explosive, degassing and, as Tilley noted, its copious development of andesites and their more felsic associates. If these rock types were derived from basalt, the principal relevant changes in major element composition are reductions in Fe, Ca and Mg, and increases in Si, Al and (Na + K). Four principal mechanisms for inducing these changes have been proposed: (1) magmatic differentiation induced by fractional crystallisation, (2) magma mixing, (3) partial melting of an ultramafic-derived basaltic parent, and (4) crustal contamination. A fifth postulate—long recognised but only occasionally seriously considered—is that loss in the volatile phase during eruption and later degassing may make a significant contribution to the overall process. On the basis that Tilley's (and others’) orogenic basalt–andesite–dacite–rhyolite series constitutes a linear arrangement on the conventional FeO_t–MgO–(Na₂O + K₂O) diagram it is shown on numerical grounds that fractional crystallisation alone cannot account for the observed compositional trend—that, while accumulates are neither uncommon nor insubstantial in amount in modern arcs, they are olivine-rich, not magnetite-rich, and that numerical, petrological and field evidence indicates that the high oxidation/magnetite subtraction hypothesis of orogenic andesite genesis can no longer be seriously entertained. The partial melting hypothesis encounters contrary numerical evidence, closely analogous with that adduced for fractional crystallisation. Magma mixing eventually encounters the difficulty of the nature of the felsic material required for rhyolite formation, and assimilation of the preservation of primitive isotope ratios as lava evolution progresses. A fifth mechanism—volatile loss—may make a significant contribution to the relevant compositional change, perhaps in combination with one or more of the other proposed processes. Geochemical, petrological and field evidence pertaining to this is reviewed and examined, and it is postulated that indeed a combination of fractional crystallisation as the principal mechanism, volatile loss as a contributing factor, provides a plausible process. A case is made for an exploratory experimental investigation of the possibility of significant loss in a gas/vapour phase.     

3种海洋硅藻不同培养阶段挥发性成分的比较分析

本文应用顶空固相微萃取气相色谱-质谱联用技术,对威氏海链藻Thalassiosira weissflogii、小新月菱形藻Nitzschia closterium、角毛藻Chaetoceros calcitrons 3种硅藻的挥发性成分进行分析。结果表明,在3种硅藻的培养过程中,其挥发性成分除了壬醛及醇类呈现先增后降的趋势外,大多数不饱和醛类的含量在不断增加,烷烯烃类物质在不断减少,而乙酸乙酯、2-甲基-2-丙酸甲酯这类酯类化合物在角毛藻衰败期会显著富集。通过对代表性饵料硅藻的挥发性成分进行研究,可为海水养殖过程中微藻投喂种类、投喂时机的选择提供理论依据,并为海洋硅藻的进一步开发奠定基础。     

Reactive trace element enrichment in a highly modified, tidally inundated acid sulfate soil wetland: East Trinity, Australia

This study examines the abundance of trace elements in surface sediments of a former acid sulfate soil (ASS) wetland subjected to marine tidal inundation. Sediment properties of this highly modified study site are compared with those of an adjacent unmodified, intertidal mangrove forest. Whilst some trace elements (Al, Cd, Mn, Ni and Zn) were clearly depleted due to mobilisation and leaching in the previous oxic-acidic phase, other trace elements (As and Cr) displayed significant enrichment in the tidally inundated ASS. Many trace elements were strongly associated with the reactive Fe and acid volatile sulfide (AVS) fractions, suggesting that trace elements may be adsorbed to abundant reactive Fe phases or sequestered as sulfide minerals. These findings provide an important understanding of the fate and mobility of reactive iron, AVS and trace elements during tidal remediation of a formerly acidified Great Barrier Reef (GBR) catchment.     

某石油化工场地土层挥发性有机物的污染特征

在调查华北平原一个污染年限超过35年的石油化工场地时,采用便携式仪器土层测气方法,快速、准确地测定了场地内40多个钻孔不同深度土层中挥发性有机物(VOCs)的浓度。基于对场地地质水文地质条件的认识,以及通过对大量数据的分析对比和应用空间变异分析方法,得出了对场地土层介质中VOCs污染特征的如下认识:(1)土层VOCs浓度的垂向变化可概括为污染源淋滤型、包气带扩散污染型、地下水波动带污染型和混合污染型四种污染类型;(2)在包气带砂土层和粉土层中,VOCs的扩散规律可近似用指数模型描述;(3)包气带土层中VOCs优先积聚在渗透性强的砂性土层中,砂土层中VOCs浓度是粉土层中VOCs浓度的1.5～12倍,平均3.76倍;(4)土层VOCs浓度的水平变异性表现为包气带土层的变异性要比地下水波动带土层大,且水平变异性能在25m尺度内得到充分显示;而土层VOCs浓度的垂向变异性随地而异,变化复杂,很难用统一的一个量化尺度来表征。本文对这一典型污染场地的剖析,有助于从事污染场地调查人员认识我国华北平原石油化工类场地的污染特征,并为调查与治理类似污染场地提供技术依据。     

中国69个城市地下水挥发性卤代烃污染检测与特征研究

为了初步掌握中国主要城市地下水挥发性卤代烃污染状况和特征,在中国69个城市开展了地下水挥发性卤代烃污染检测与特征研究,采集地下水样品791组,采样井均为工农业生产和生活饮用水水井;依据US EPA 8260B检测方法,采用气相色谱/质谱联用分析仪器(P&T-GC/MS),分析和测试了氯仿、四氯化碳、1,1,1-三氯乙烷、三氯乙烯、四氯乙烯和二氯甲烷等15种挥发性卤代烃的质量浓度。结果表明:在791组地下水样品中,有406组样品至少有一种挥发性卤代烃组分被检出,检出率为51.33%;各组分中,氯仿的检出率最高,为20.35%,其他组分的检出率为0.25%～5.06%;氯乙烯在所有样品中均未检出;有13组样品的单项组分超标,超标率为1.64%;超标率由高到低分别为四氯化碳(0.76%)、氯仿(0.25%)、1,2-二氯乙烷(0.25%)、三氯乙烯(0.13%)、1,1,2-三氯乙烷(0.13%)、1,2-二氯丙烷(0.13%);超标井均为非供水水源地水井。检测与研究结果表明:中国主要城市地下水挥发性卤代烃污染物检出率较高,检测的69个城市中71%的城市至少有一种挥发性卤代烃被检出,且潜水的检出率高于承压水,但总体超标率较低。     

Origin of light volatile hydrocarbon gases in mud volcano fluids, Gulf of Cadiz — Evidence for multiple sources and transport mechanisms in active sedimentary wedges

Widespread mud volcanism across the thick (≤ 14 km) seismically active sedimentary prism of the Gulf of Cadiz is driven by tectonic activity along extensive strike–slip faults and thrusts associated with the accommodation of the Africa–Eurasia convergence and building of the Arc of Gibraltar, respectively. An investigation of eleven active sites located on the Moroccan Margin and in deeper waters across the wedge showed that light volatile hydrocarbon gases vented at the mud volcanoes (MVs) have distinct, mainly thermogenic, origins. Gases of higher and lower thermal maturities are mixed at Ginsburg and Mercator MVs on the Moroccan Margin, probably because high maturity gases that are trapped beneath evaporite deposits are transported upwards at the MVs and mixed with shallower, less mature, thermogenic gases during migration. At all other sites except for the westernmost Porto MV, δ¹³C–CH₄ and δ²H–CH₄ values of ~ − 50‰ and − 200‰, respectively, suggest a common origin for methane; however, the ratio of CH₄/(C₂H₆ + C₃H₈) varies from ~ 10 to > 7000 between sites. Mixing of shallow biogenic and deep thermogenic gases cannot account for the observed compositions which instead result mainly from extensive migration of thermogenic gases in the deeply-buried sediments, possibly associated with biodegradation of C₂₊ homologues and secondary methane production at Captain Arutyunov and Carlos Ribeiro MVs. At the deep-water Bonjardim, Olenin and Carlos Ribeiro MVs, generation of C₂₊-enriched gases is probably promoted by high heat flux anomalies which have been measured in the western area of the wedge. At Porto MV, gases are highly enriched in CH₄ having δ¹³C–CH₄ ~ − 50‰, as at most sites, but markedly lower δ²H–CH₄ values < − 250‰, suggesting that it is not generated by thermal cracking of n-alkanes but rather that it has a deep Archaeal origin. The presence of petroleum-type hydrocarbons is consistent with a thermogenic origin, and at sites where CH₄ is predominant support the suggestion that gases have experienced extensive transport during which they mobilized oil from sediments ~ 2–4 km deep. These fluids then migrate into shallower, thermally immature muds, driving their mobilization and extrusion at the seafloor. At Porto MV, the limited presence of petroleum in mud breccia sediments further supports the hypothesis of a predominantly deep microbial origin of CH₄.