Cl/Br of scapolite as a fluid tracer in the earth's crust: insights into fluid sources in the Mary Kathleen Fold Belt,Mt. Isa Inlier,Australia

A combination of analytical methods, including trace element analysis of Br in scapolite by LA‐ICP‐MS, was employed to unravel the fluid–rock interaction history of the Mary Kathleen Fold Belt of northern Australia. Halogen ratios in the metamorphic and hydrothermally derived scapolite from a range of rock‐types record interaction between the host rocks and magmatic‐hydrothermal fluids derived from granite plutons and regional metamorphism. The results show that halite‐dissolution supplied at best only minor chlorine to fluids in the Fold Belt. Chlorine/bromine ratios in metamorphic scapolite indicate that fluids were dominantly derived from basinal brines formed from sub‐aerial evaporation of seawater beyond the point of halite saturation. This bittern fluid infiltrated the underlying sedimentary sequences prior to regional metamorphism. Zoned scapolite in a major late metamorphic mineralized shear‐zone records three discrete pulses of magmatic and metamorphic fluid, and it is suggested that fluid mixing may have assisted mineralization along and around this shear‐zone. As a crucial prerequisite for halogen fluid tracer studies using scapolite, we find in our samples that Cl and Br do not fractionate when incorporated in scapolite. Furthermore, unaltered rims of heavily retrogressed scapolite show indistinguishable Cl/Br signatures compared with fresh grains from the same sample indicating retrograde metamorphism did not significantly affect Cl and Br signatures in scapolite group minerals.     

流动注射夹层带进样方式分光光度法测定溴

采用流动注射夹层带进样方式研究了酚红法测定溴的化学条件和流路参数，所建立的方法具有灵敏度高、精密度好、试剂消耗量少和分析速度快的特点。在所选实验条件下，Ｂｒ－的质量浓度为０２～１００ｍｇ／Ｌ时有良好的线性关系，检出限和相对标准偏差（２０ｍｇ／ＬＢｒ－，ｎ＝１１）分别为０１１ｍｇ／Ｌ和０８８％，测定速度为６０～９０／ｈ。对化学试剂ＫＣｌ和ＮａＣｌ中的杂质溴进行了测定，加标回收率为９５％～１０５％。     

溴素的有机化学Ⅵ.多溴代邻羟基苯甲酸—2,3,5,6—四溴—1,4—苯二酯的合成

由邻羟基苯甲酸、１，４—苯二酚和溴素起始，经溴代、氧化—溴代、形成酰氯和酰化等步骤，合成了三种新的多溴代邻羟基苯甲酸—２，３，５，６—四溴—１，４—苯二酯。通过对产物溴含量、ＩＲ和１ＨＮＭＲ的分析，验证了产物的结构     

中国含盐盆地卤水溴元素分布与物源

中国含盐盆地赋存丰富的盐湖卤水和深部卤水资源,卤水中富集溴(Br)元素,具有潜在的开发利用价值。Br作为盐湖卤水中重要的资源元素,目前对其分布规律和物质来源的系统对比研究鲜有报道。本文以柴达木盆地察尔汗盐湖四个区段晶间卤水为研究对象,分析整个湖区Br元素分布规律和物质来源,对比中国不同含盐盆地卤水Br资源变化和物源联系,并总结不同卤水开发利用价值。结果表明：① 察尔汗盐湖Br含量呈东高西低特征且不同区段差异明显;② 别勒滩和达布逊区段卤水低Br受河流补给并经蒸发富集,而察尔汗和霍布逊区段高Br受北部断裂带上涌富Ca泉水补给;③ 中国含盐盆地(柴达木盆地、库车盆地、江汉盆地、吉泰盆地)大部分深部卤水高Br值主要受水- 岩反应、沉积物及有机质中Br的解吸获得;④ 盐湖晶间卤水虽远不及深部卤水Br含量高,但其优点在于便于开发、综合利用率高,尤其浓缩卤水及老卤中的Br含量可预见性的高于工业开采品位,是当下和今后值得关注的资源。     

The F,Cl, Br and I Contents of Reference Glasses BHVO‐2G,BIR‐1G,BCR‐2G,GSD‐1G,GSE‐1G,NIST SRM 610 and NIST SRM 612

Halogen contents for the widely distributed reference glasses BHVO‐2G, BIR‐1G, BCR‐2G, GSD‐1G, GSE‐1G, NIST SRM 610 and NIST SRM 612 were investigated by pyrohydrolysis combined with ion chromatography, total reflection X‐ray fluorescence analysis, instrumental neutron activation analysis, the noble gas method, electron probe microanalysis and laser ablation‐inductively coupled plasma‐mass spectrometry. Glasses BHVO‐2G, GSD‐1G and GSE‐1G have halogen contents that can be reproduced at the 15% level by all bulk techniques and cover a significant range in halogen mass fractions for F (~ 20–300 μg g^?1), Cl (~ 70–1220 μg g^?1) and Br (~ 0.2–285 μg g^?1) and I (~ 9–3560 ng g^?1). The BIR‐1G glass has low F (< 15 μg g^?1), Cl (~ 20 μg g^?1), Br (15 ng g^?1) and I (3 ng g^?1). The halogen contents for the silica‐rich NIST SRM 610 and 612 glasses were poorly reproduced by the different techniques. The relatively high Cl, Br and I abundances in glasses GSD‐1G and GSE‐1G mean that these glasses are well suited for calibrating spatially resolved micro‐analytical studies on silicate glasses, melt and fluid inclusions. Combined EPMA and laser ablation‐inductively coupled plasma‐mass spectrometry data for glass GSE‐1G demonstrate homogeneity at the 10% level for Cl and Br.     

青藏高原盐湖卤水中溴的分布特征及来源初探

溴是完备工业体系的关键必备元素。盐湖卤水是溴的重要来源。青藏高原盐湖众多,富含钾、锂、硼等资源元素,开发潜力巨大。然而,目前针对青藏高原盐湖溴浓度、分布特征及其物源的研究仍然薄弱。本次研究采集了26个青藏高原盐湖表卤水样品并分析其溴浓度,进一步总结其他64个已报道盐湖数据,系统分析了青藏高原盐湖溴浓度分布特征,并进一步探讨了溴的可能物源。结果表明:青藏高原盐湖表卤水溴分布在0.5～246.8 mg/L之间,平均为41.1 mg/L,其中,碳酸盐型盐湖卤水平均溴浓度最高(47.0 mg/L),且集中分布在高原南部,而氯化物型盐湖平均溴浓度最低(30.1mg/L),盐湖溴浓度呈现自南向北降低的趋势;青藏高原盐湖中溴有多种来源,高原南部富溴盐湖溴的来源可能主要与热泉补给有关,而柴达木盆地盐湖高溴来源可能主要与深部地层水(如油田水、背斜构造裂隙孔隙水、砂砾孔隙卤水、气田水等)补给有关。     

阴离子交换色谱-电感耦合等离子体质谱联用技术用于面粉中溴形态分析

建立的阴离子交换色谱-电感耦合等离子体质谱联用技术用于测量面粉中的痕量 BrO3-及Br-。使用DIONEX CarBoPac PA-100(4 mm×250 mm,i．d．)色谱柱,在流速1 mL／min 及5 mmol／L NH4NO3淋洗液下分离BrO3-和Br-。该方法在100μL进样量下BrO3-的检出限为 0．0027 μmoL／L(0．22μg／L),Br-为0．0067 μmoL／L(0．54μg／L)。对市场上部分面粉类样品的分析结果表明,所选面粉只有一种检出有BrO3-,其他样品中的BrO3-均低于检出限。方法的回收率可达到98％-109％。     

High resolution spectral features of a series of aromatic hydrocarbons and BrO: Potential interferences in atmospheric OH-measurements

Naphthalene (C₁₀H₈), several other hydrocarbons, mostly derivates of naphthalene, and bromine oxide (BrO) were analyzed for narrow band (0.01 nm) absorption lines in the wavelength range between 307.7 and 308.3 nm to study their potential impact on OH radical measurements by differential absorption spectroscopy.Only naphthalene showed narrow band absorption lines in this wavelength region. From nine naphthalene lines the differential absorption cross-section was determined.The strongest naphthalene line at 308.002 nm is close to the Q ₁(2) OH line, but about a factor of 200 weaker (=(65.2±15.3)×10^-20 cm²/molec). The corresponding detection limit for naphthalene is about 15 ppt. We re-evaluated some spectra of our OH measurement campaign in July 1987 with respect to naphthalene and obtained an upper limit of 30 ppt for its concentration.BrO was recorded in the larger wavelength interval between 307.7 and 308.7 nm. Structured absorptions were only observed at wavelengths above 308.2 nm and no significant structures were found in the vicinity of the Q ₁(2) and Q ₁(3) OH lines.     

南极大陆沿岸地面臭氧损耗事件的研究

利用南极大陆沿岸中山站2008-2013年的地面臭氧连续观测数据和相关资料,对地面臭氧损耗事件（ODE）进行研究。结果显示,春季南极中山站常发生臭氧损耗事件。在该事件发生期间,气象要素有明显的突变过程,包括气温明显下降,风向由偏东风转变为偏北风,风速随之下降。来自海冰区的偏北风增多,风速很小,使臭氧浓度维持在较低水平。地面臭氧损耗事件主要与南极沿岸海冰区的活性溴（BrO）浓度有关。春季南极大陆沿岸海冰冻融过程中形成的冰间水道和冰间湖,在低温的作用下会再次冻结,形成薄冰和霜花。卫星资料能够观测到薄冰区释放的活化海盐溴高浓度区,活性溴与臭氧发生化学反应形成地面臭氧损耗事件。臭氧损耗现象是在未受到人为影响的自然状态下发生的,与中高纬度地区光化学反应导致臭氧消耗有所不同。      

超声提取-离子色谱法测定铁矿石中水溶性氟氯溴及硝酸根

铁矿石样品经超声提取、离心机分离沉淀后,分别通过IC-RP柱、IC-Na柱及0.22μm微孔过滤膜过滤,25.00 mmol/L NaOH溶液作为淋洗液,利用AS-19型阴离子分离柱和ASRS 300-4 mm连续自动再生化学抑制器分离样品中氟、氯、溴和硝酸根多种水溶性阴离子和采集数据。经过IC-RP柱可吸附样品溶液中有机质,通过IC-Na柱可将溶液中重金属离子置换成Na+,使之与淋洗液的阳离子成分一致。对水溶性阴离子的提取效率进行实验,确定提取时间为30 min。在标准溶液及待测样品溶液中加入一定量相应的淋洗液,使溶液和淋洗液的电导值相匹配来消除水负峰的影响。F-、Cl-、Br-、NO3-的方法检出限分别为2.1、3.5、2.5、2.0μg/g,工作曲线的相关系数>0.999。用铁矿石标准样品GBW 07218a验证方法的准确度与精密度,测定值与标准值基本吻合,精密度(RSD,n=10)小于5%,加标回收率为96%～104%。用于实际样品的分析,测定值与离子选择电极法结果接近。方法线性范围宽,操作简单,快速高效,适用于实验室日常检测工作。