基于高分二号卫星数据的煤矿区地质灾害信息提取研究

随着遥感数据获取技术和能力的全面提高,遥感数据呈现出明显的大数据特征。发展适应于遥感大数据的智能分析和信息挖掘技术,成为当前遥感技术研究的前沿。高分二号（GF-2）卫星数据是我国首颗自主研发的亚米级高分辨率卫星数据,具有观测幅宽、重访周期短、高辐射精度、高定位精度等优势,为未来我国地质灾害的长期、动态地监测和研究提供了高精度、稳定可靠的数据源。本文选取安徽谢桥煤矿2015年1月8日的GF-2卫星影像为研究数据,在对煤矿区主要地质灾害遥感地学分析的基础上,采用面向对象的影像分析方法对研究区由采煤活动所诱发的地质灾害信息进行自动提取。结果表明：利用GF-2卫星数据能够有效地识别地质灾害体的位置、范围、形态等空间分布特征;面向对象的自动提取方法对于煤矿区大面积的积水塌陷盆地、小规模的塌陷坑和线性的地裂缝都有很高的提取精度,识别精度达90% 以上;基于逐层剔除的思路构建的提取规则,为GF-2数据在地质灾害调查和大数据分析中的应用提供了很好的技术支持,也为其它地物目标的提取提供了参考,但在特征的选择和阈值的设定上需要具体分析。     

Visual MODFLOW在煤矿建设地下水环境影响评价中的应用 ——以甘肃省灵台县安家庄煤矿为例

结合甘肃省灵台县安家庄煤矿地下水环境影响评价实例,建立了评价区水文地质概念模型,并基于Visual MODFLOW对评价区地下水进行了数值模拟计算和验证;预报了设计开采条件下研究区不同含水层的地下水水位。预报结果表明:矿坑排水使得煤层所在含水层出现疏干现象,并且疏干范围随着开采范围的增加而不断扩大;在煤矿开采作用下,随着模拟时间的延续,煤系层上覆白垩系洛河组—宜君组含水层地下水位降落漏斗的范围及地下水位下降幅度不断增大,但降落漏斗的范围基本上不超过采空区范围;煤矿开采对白垩系环河组含水层无影响,至矿区开采期结束,未引起含水层水位下降;对上部孔隙、裂隙潜水含水层也无影响,至矿区开采期结束未引起含水层水位下降。     

几内亚福雷卡里亚YML铁矿区的富铁矿床地质特征及找矿前景探讨

YML铁矿区位于几内亚福雷卡里亚省,富铁矿以条带状赤铁矿和铁角砾岩矿为主。矿区内共发育7条矿体,条带状赤铁矿体6条,铁角砾岩矿体1条。条带状赤铁矿体赋存部位多为向形地段,次级紧密褶皱发育,沿走向和倾向有逐渐变薄和尖灭的趋势;铁角砾岩矿体覆盖于地表,以风化壳的形式出现。矿床类型属复合类型,即海底热液喷气沉积叠加后期构造变质型+风化淋滤型。该区具备铁矿形成和保存的地质条件,且已发现具一定储量、品位较高的条带状赤铁矿和大面积的铁角砾岩分布区,区内铁矿找矿远景较好。     

基于ASTER与Sentinel-2A融合数据的云南普朗铜矿化蚀变信息提取

云南普朗铜矿区是我国提高战略性金属矿产铜矿资源的主要潜力地段,该矿区位于多云多雨山地高原区,采用传统地面调查方法开展找矿勘查工作受限较大,而遥感技术可在其中发挥重要作用。鉴于此,本研究选取ASTER和Sentinel-2A多光谱遥感数据,在光谱协同统一两种数据源的地表反射率基础上,采用高通滤波(High-Pass Filtering,HPF)的融合方法兼顾两种数据在短波红外波段和可见光近红外波段的优势,获取了具有高空间分辨率和高光谱保真度的ASTER-Sentinel-2A融合数据集;进而利用"比值+主成分分析法"与"主成分分析+能谱-面积法",开展了普朗铜矿区矿化遥感蚀变信息识别,并通过深入分析及野外验证,提出了对普朗铜矿蚀变信息分布特征及找矿潜力地带的新认识:(1)在原蚀变填图工作中判定为青磐岩化带的东部区域,重新进行了蚀变带的划分;(2)东部区域中新划分的钾化硅化带和绢英岩化带,具有较大找矿潜力。本研究可为普朗铜矿找矿勘查提供参考。     

蚀变矿物填图技术在斑岩型铜矿找矿勘查中的应用—以滇西北香格里拉松诺矿床为例

松诺铜矿区位于香格里拉格咱斑岩铜矿带红山-普朗铜多金属成矿亚带中段,矿区剥蚀程度较低,具有寻找斑岩型铜矿的潜力。本次蚀变矿物填图工作采用近红外光谱矿物分析技术,识别出绿泥石、绿帘石、高岭石、云母类、蒙脱石类及伊利石等6类主要蚀变矿物,蚀变类型为青磐岩化、绢英岩化;结合物探、化探异常分布,圈定3处找矿靶区,经对KHT2、KHT3钻孔验证,深部均圈定多层铜矿化体。结果表明,近红外光谱矿物分析技术在斑岩型铜多金属矿床勘查评价中可以较好地划分热液矿化蚀变带,进一步明确斑岩型矿化-蚀变中心,为探矿工程部署提供依据。     

Contrasting water–rock interaction behaviors of antimony and arsenic in contaminated rivers around an antimony mine,Hunan Province,China

Although antimony (Sb) and arsenic (As) exhibit similar geochemical behavior and toxicity in the environment, growing evidence suggests that their water–rock interaction behavior in contaminated rivers is quite different. Twenty-nine river water samples were collected between September and November 2018 from contaminated rivers around an antimony mine in Hunan Province, China. The concentrations of As and Sb were inversely proportional to the water flow distance. The rates and magnitudes of Sb decrease were more prominent than those of As. Silicate mineral dissolution from rocks such as silicified limestone increased the As and Sb concentration of in-mine-district (IMD) water. Dissolution of carbonate minerals, ion exchange, and competitive adsorption were the major water–rock interactions, resulting in rapidly decreasing As and Sb concentration in IMD direct impacted water and IMD indirect impacted water. The behaviors of As and Sb during water–rock interaction were dissimilar for areas dominated by carbonate and silicate minerals.     

黄原胶改性微米铁修复地下水中Cr(Ⅵ)污染的试验

为了解决微米铁的重力沉降问题,提高微米铁修复地下水Cr（Ⅵ）污染的原位修复效果,本文利用黄原胶对微米铁进行改性,并通过沉降实验探究改性微米铁浆液的稳定性,同时选择Cr（Ⅵ）作为目标污染物,探究黄原胶改性微米铁去除地下水Cr（Ⅵ）污染的降解能力。实验结果显示：当黄原胶的投加质量浓度分别为0.0、1.0、1.5、2.0、2.5、3.0、6.0 g/L时,改性微米铁浆液的悬浮稳定性逐渐得到加强,在5 h沉降实验结束时,对应的相对分光光度值分别为0.05、0.25、0.46、0.57、0.65、0.73和0.87;黄原胶具有抑制微米铁吸附Cr（Ⅵ）的能力,其可促进Cr（Ⅵ）的还原,提高Cr（Ⅵ）的去除率;随着黄原胶投加质量浓度的增加,对应的Cr（Ⅵ）去除率分别为33.4%、41.2%、47.4%、51.1%、53.0%、63.9%和64.1%;6.0 g/L黄原胶改性的微米铁浆液具有最佳的悬浮稳定性,黄原胶的投加提高了微米铁的反应活性,但当黄原胶投加质量浓度超过3.0 g/L时,其对Cr（Ⅵ）的去除率没有显著提高;黄原胶投加质量浓度越大,黄原胶的缓冲作用就越明显。     

对甘肃矿山生态保护修复资金管理的思考及建议

矿山开采生产的生态保护与修复工作,涉及自然资源、生态环境、水利、林草等多部门,结合矿政管理工作实际,梳理了矿山生态保护修复资金类型,总结剖析了目前不同部门分头管理存在的问题,在此基础上,提出应整合各部门矿山生态保护修复方案及资金,形成管理合力,把生态保护修复工作贯穿到从地质勘查、矿山建设、开采、闭坑、管护的全过程,边开采边治理,整体保护,综合整治,系统修复。     

白云鄂博矿床东矿段深部及白云向斜核部探矿的可行性探讨

白云鄂博东矿（铁矿石）已属于轻度危机矿山,解决白云鄂博东矿的资源接续问题已迫在眉睫。依据老地质资料和生产过程中的新发现,参考多位矿床成因研究专家的成果,笔者等认为在白云鄂博东矿体深部及白云向斜核部探矿是可行的。     

Adsorption of Pentachlorophenol onto Oxide and Clay Minerals： Surface Reaction Model and Environmental Implications

The adsorption of pentachlorophenol （PCP） onto quartz, kaolinite, illite, montmorillonite and iron oxides has been investigated by batch equilibrium techniques. The pH-dependent isotherms are curves with peak values, the position of which is at about pH = 5-6 depending on the mineral species. Based on distribution of both speciation of surface hydroxyls on minerals and PCP in solution a surface reaction model involving surface complexation and surface electrostatic attraction is presented to fit the pH-dependent isotherms, and both reaction constants are calculated. The results show that on quartz and phyllosilicate minerals the predominant adsorption reaction is surface complexation, meanwhile both of surface electrostatic attraction and surface complexation are involved on the iron oxide minerals. The reaction constants of surface electrostatic adsorption are usually one to three orders in magnitude, larger than that of surface complexation. The concentration-dependent isotherms can be well fitted by Langmnir equation with the correlation coefficient R〉0.93 for kaolinite and iron oxides. The maximum adsorption is found in the order： hematite 〉 lepidocrocite 〉 goethite 〉 kaolinite 〉 quartz 〉 montmorillonite ≈ illite, which can be interpreted by consideration of both reaction mechanism and surface hydroxyl density. The significant adsorption of PCP onto mineral surfaces suggests that clay and iron oxide minerals will play an important role as HIOCs are adsorbed in laterite or latertoid soil, which is widespread in South China.