流量替代渗透率评价破碎性储层工作流体伤害程度

若地层岩石整体强度偏低,在力学环境改变后岩石易破碎成不规则破裂体,则储存油气资源的此类破碎地层被称为破碎性储层。由于破碎性储层在纵向上存在着较强的非均质性,通过测试单个柱塞岩样在工作流体伤害前后的渗透率变化难以体现工作流体对储层的整体伤害程度。为此,利用达西定律先从理论上探讨用流量替代渗透率定量表征储层伤害程度的可行性,再开展单层开采、双层及三层并采的流量测试实验,评价工作流体对单层、多层储层的整体伤害程度,并将流量损害率与渗透率损害率进行对比以求证流量替代渗透率的可行性。研究结果表明:①单层开采时,流量损害率与渗透率损害率基本一致,渗透率损害率是流量损害率的一种特殊形式;②双层及三层并采时,单层各自稳定流量损害率与渗透率损害率接近,且流量损害率可以定量表征并采储层的整体伤害程度,而渗透率损害率则无法定量表证;③稳定流量损害率较累积流量损害率更接近渗透率损害率。结论认为,测定稳定流量可以替代测定渗透率评价工作流体对破碎性储层的伤害程度,从而为优选工程技术与评价工作流体的适应性提供了方法依据。     

物质平衡-拟压力近似条件法确定气藏储量

物质平衡法作为一种有效的手段被广泛应用于气藏储量或井控储量的确定。为简便准确地确定气藏储量，笔者从物质平衡原理出发导出了"物质平衡条件"，求解气体渗流数学模型，得到了"拟压力近似条件"。将二者结合，提出了"物质平衡-拟压力近似条件法"（MB-QAC方法）。利用该方法，通过边界控制流阶段（产量波动相较于边界作用可忽略）的生产数据便可准确地计算气藏储量。定产量、定流压以及复杂生产计划条件下的数值模拟数据以及气藏实例验证了其有效性。在生产数据记录可靠的条件下，储量计算误差一般小于5%。同时，数值模拟结果表明，动态物质平衡方程是一种近似关系，拟压力近似条件对于模拟的各种情形均成立。由于考虑了岩石和束缚水的压缩性、气井产量的波动和气体性质的变化，MB-QAC方法具有一定的理论基础，对于异常高压和正常压力系统的气藏均适用，但不适用于水体活跃的气藏。     

基于GF-1数据的三峡库区水体信息精细化提取

为实现江河类狭长型水体信息的精细化提取，利用GF-1卫星数据，采用支持向量机和目视解译相结合的方法对三峡库区及重庆市水体信息进行了精细化提取。使用总体分类精度、Kappa系数、错分误差、漏分误差、制图精度和用户精度等指标对库区水体信息粗提取结果进行验证分析。结果表明:4个试验区水体提取的总体分类精度均超过90%，除试验区4的Kappa系数为0.884 1以外，其余试验区均超过0.9，提取精度较高。结合目视解译的方法，在粗提取结果的基础上对各问题进行精细化处理，得到精度高、完整性好的三峡库区以及重庆市水体信息数据，可为后续该区域的精细化遥感业务开展提供有效资料。     

Pressure transient analysis for asymmetrically fractured wells in dual-permeability organic compound reservoir of hydrogen and carbon

In this paper, a comprehensive semi-analytical model was presented to investigate pressure transient behavior for asymmetrically fractured wells in organic compound reservoir of hydrogen and carbon with dual-permeability behavior. Stehfest inversion algorithm can be used to transform it back into time domain to obtain pressure solution. The presented solution was validated well with numerical solutions. Flow characteristics for asymmetrically fractured wells in dual-permeability organic compound reservoir of hydrogen and carbon were divided into five regime. The effects of some important parameters on dimensionless pressure and its derivative curves were analyzed in details, including inter-porosity flow coefficient from matrix to natural fractures λ, storage coefficient ω, fracture asymmetry factor θ and permeability ratio κ. The presented model can be used to predict production performance and do well test analysis in the development of dual-permeability organic compound reservoir of hydrogen and carbon.     

分光光度法和光度滴定法联合测定湿法炼锌流程中钴渣浸出液中锌钴镍

湿法炼锌流程中钴渣浸出液中含有高浓度的Fe²⁺和Mn²⁺,用分光光度法测定Co²⁺和Ni²⁺时,Fe²⁺-EDTA会严重干扰Co²⁺和Ni²⁺的测定;在用光度滴定法测定Zn²⁺和Co²⁺合量时,Ni²⁺对二甲酚橙指示剂具有封闭作用,Mn²⁺亦与EDTA螯合,导致滴定结果偏高。为消除Fe²⁺和Mn²⁺对Zn²⁺、Co²⁺和Ni²⁺测定的干扰,实验进行氧化分离Fe²⁺和Mn²⁺预处理,在NaAc/Hac缓冲体系下,以EDTA作显色剂用分光光度法测定Co²⁺、Ni²⁺。在波长466nm处,Co²⁺的线性范围为50~500mg/L时与吸光度呈线性,相关系数R²为0.9992;在384nm处,Ni²⁺的线性范围为50~500mg/L时与吸光度呈线性,相关系数R²为0.9998。根据分光光度法测出Ni²⁺物质的量,加入1.1倍的丁二酮肟以除去Ni²⁺,用二甲酚橙为指示剂,EDTA鳌合-光度滴定法测定Zn²⁺、Co²⁺合量,扣减Co²⁺含量得出Zn²⁺含量。选取4个锌湿法炼锌流程中钴渣浸出液实际样品,按照实验方法中的分光光度法测定Co²⁺和Ni²⁺,光度滴定法测定Zn²⁺、Co²⁺合量,Zn²⁺、Co²⁺和Ni²⁺测定结果的相对标准偏差(RSD,n=6)均不大于0.70%,加标回收率分别为99.59%~100.41%、99.69%~100.64%、99.92%~100.08%。     

电感耦合等离子体原子发射光谱法测定土壤中8种组分

为满足土地质量调查的需求,实现土壤中多组分的同时消解及准确测定,提高大批量样品的分析效率,建立了土壤样品经高压密闭消解后,采用电感耦合等离子体原子发射光谱法(ICP-AES)测定K₂O、Na₂O、CaO、MgO、Ba、Mn、Cu、Zn的方法。通过对消解体系、酸用量、消解温度等方面的考察,确定最佳实验条件;并对待测液中共存元素Al、Fe的干扰进行探讨,两者均不干扰测定。各组分校准曲线线性相关系数均大于0.999;检出限为0.01~10μg/g。实验方法用于测定土壤标准样品GBW07385、GBW07386、GBW07388中K₂O、Na₂O、CaO、MgO、Ba、Mn、Cu、Zn,测定结果的相对标准偏差(RSD,n=12)为1.1%~4.3%,相对误差RE为-4.0%~4.6%。采用实验方法对土壤实际样品中K₂O、Na₂O、CaO、MgO、Ba、Mn、Cu、Zn进行测定,结果的RSD(n=6)为1.2%~4.6%;并与地矿行业标准方法DZ/T 0279.2—2016测定结果进行比对,测得结果基本一致。     

高炉喷吹煤粉燃烧性与反应性的研究与应用

为了研究高炉喷吹煤粉的冶金性能，采用热重分析法对6种无烟煤和1种烟煤进行燃烧性与反应性研究。结果表明，与无烟煤相比，烟煤在不同温度下的燃烧性和反应性均明显高于无烟煤。混煤的燃烧率实测值大于加权值，使用混煤可以发挥无烟煤和烟煤各自的优点，加快燃烧过程，提高混煤燃烧率。随着混煤中粒度小于74 μm煤粉所占比例的增加，燃烧率增大。在高煤比喷吹条件下，混煤煤粉粒度小于74 μm的比例控制在75%左右。结合无烟煤的燃烧性和反应性试验结果，建议喷吹煤粉采购中应尽可能多地采购无烟煤C资源，同时控制无烟煤E的采购量；高炉提煤比操作中应将无烟煤C确定为喷吹用无烟煤的首选煤种，以提升混煤燃烧率和发挥未燃煤粉保护焦炭的作用。     

Twenty-five years of total antioxidant capacity measurement of foods and biological fluids: merits and limitations

This review summarises 25 years of investigations on antioxidants research in foods and biological fluids and critically analyses the merits and limitations of using the total antioxidant capacity (TAC) measurement in the metabolomic era. An enormous bulk of knowledge was produced regarding the antioxidant capacity of foods and large TAC databases were developed. A direct link between a food TAC value and any health benefit is erroneous and has led to several cases of consumer deception. However, the striking epidemiological evidence associating a high dietary TAC with some disease prevention and the availability of well-constructed TAC databases deserve attention and must be taken into account to establish the usefulness of measuring TAC in both foods and biological samples. The in vivo TAC measurement, usually performed in plasma, is influenced by many external factors, such as dietary habits, as well as environmental and behavioural factors, which are integrated towards homeostatic control by fine physiological mechanisms with high inter-individual variability. Therefore, plasma TAC cannot be considered as a unique biomarker of individual antioxidant status. However, the combined evaluation of plasma TAC with known markers of disease, individual metabolism, inflammation and genetics, as well as with markers of gut microbiota composition and activity, may lead to the identification of populations that are more responsive to food/diet TAC. In this framework, the appropriate use of TAC measurement both in food and in vivo can still provide support for the interpretation of complex phenomena and be a tool for sample screening when making a quick decision toward in-depth research investigations. © 2018 Society of Chemical Industry