Ca(OH)2解吸并固定混合吸收液中CO2的实验研究

CO₂化学吸收法分离纯度高,技术成熟,但能耗过高及成本是困扰该技术发展的瓶颈.在常压条件下对利用Ca（OH）₂直接矿物碳酸化固定MDEA/PZ混合吸收富液中CO₂进行了一系列实验研究,考察了吸收液负荷、Ca（OH）₂投加量、pH、温度及搅拌速率等因素对解吸率的影响,并利用动态吸收-解吸循环实验研究了其CO₂吸收性能和循环使用稳定性,最后对碳酸化反应产物进行了XRD、TEM分析.结果表明,在常压条件下,Ca（OH）₂可以通过液相直接矿物碳酸化对CO₂进行直接固定,并实现吸收富液的再生;随着负荷的升高及Ca（OH）₂投加量、pH、搅拌速率的增大,解吸率随之增加;随着溶液温度升高,解吸率下降;经过5次动态吸收-解吸循环实验后CO₂吸收量可以达到并保持在0.57 mol·L^-1,显示出了良好的循环稳定性.     

Effect of substituents in hydroxyl radical-mediated degradation of azo pyridone dyes: Theoretical approaches on the reaction mechanism

Understanding the degradation behavior of azo dyes in photocatalytic wastewater treatment is of fundamental and practical importance for their application in textile-processing and other coloration industries. In this study, quantum chemistry, as density functional theory, was used to elucidate different degradation pathways of azo pyridone dyes in a hydroxyl radical (HO^?)-initiated photocatalytic system. A series of substituted azo pyridone dyes were synthesized by changing the substituent group in the para position of the benzene moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The effect of dye molecular structure on the photocatalytic degradation reaction mechanism was analyzed and quantification of substituent effects on the thermodynamic and kinetics parameters was performed. Potential energy surface analysis revealed the most susceptible reaction site for the HO^? attack. The calculated reaction barriers are found to be strongly affected by the nature of substituent group with a good correlation using Hammett σ_p constants and experimentally determined reaction rates. The stability of pre-reaction complexes and transition state complexes were analyzed applying the distortion-interaction model. The increased stability of the transition state complexes with the distancing from the substituent group has been established.     

Plasmonic silver/silver oxide nanoparticles anchored bismuth vanadate as a novel visible-light ternary photocatalyst for degrading pharmaceutical micropollutants

The degradation of pharmaceutical micropollutants is an intensifying environmental problem and synthesis of efficient photocatalysts for this purpose is one of the foremost challenges worldwide. Therefore, this study was conducted to develop novel plasmonic Ag/Ag₂O/BiVO₄ nanocomposite photocatalysts by simple precipitation and thermal decomposition methods, which could exhibit higher photocatalytic activity for mineralized pharmaceutical micropollutants. Among the different treatments, the best performance was observed for the Ag/Ag₂O/BiVO₄ nanocomposites (5 wt.%; 10 min's visible light irradiation) which exhibited 6.57 times higher photodegradation rate than the pure BiVO₄. Further, the effects of different influencing factors on the photodegradation system of tetracycline hydrochloride (TC-HCl) were investigated and the feasibility for its practical application was explored through the specific light sources, water source and cycle experiments. The mechanistic study demonstrated that the photogenerated holes (h⁺), superoxide radicals (?O₂^?) and hydroxyl radicals (?OH) participated in TC-HCl removal process, which is different from the pure BiVO₄ reaction system. Hence, the present work can provide a new approach for the formation of novel plasmonic photocatalysts with high photoactivity and can act as effective practical application for environmental remediation.     

典型铅锌矿化区不同土地利用类型土壤重金属污染特征与评价

选取云南者海典型铅锌矿区周边冶炼区（A）、粮食主产区（B）、保护区（C）三个区域土壤为研究对象,分析三个区域内林地（LD）和耕地（GD）土壤pH、总碳（TC）、总氮（TN）、总磷（TP）和5种重金属（Hg、Cd、Pb、Zn、Cu）含量,利用典范对应分析（CCA）研究不同土地利用类型下它们之间的关系,基于系统熵值与重金属生物毒性改进灰色聚类评价法对研究区重金属污染程度进行评价。结果表明,A、B、C三区土壤的5种重金属均超过云南省土壤背景值,且含量A区 > B区 > C区,所有土壤样品Hg、Cd、Pb、Zn、Cu平均含量分别为7.24、1.53、1 794、2 892、210 mg/kg;LD土壤重金属含量普遍高于GD。研究区土壤pH总体呈弱酸性,但A区土壤受矿业活动影响呈弱碱性。TC、TN含量和C/N值均表现出LD大于GD,但TP含量表现为GD显著大于LD （P<0.05）。CCA分析表明LD和GD土壤pH与Cd和Cu呈负相关,与Zn和Pb呈正相关,且pH对重金属含量的影响最大;TC、TP与重金属Cd和Cu在LD土壤中呈正相关,在GD土壤中呈负相关。改进灰色聚类评价结果表明重金属污染程度均表现为LD大于GD;A区污染最严重且均呈重度污染,B区次之,C区污染程度最轻。经比较本文改进的灰色聚类评价法在准确性和灵敏度方面优于传统方法。     

安徽月山地区成岩-成矿作用关系研究

安徽月山地区的成岩-成矿作用在长江中下游地区具一定的典型性。本文论述了月山地区成岩-成矿的时空关系，探讨了岩浆岩及岩浆演化的成矿作用显示，并从成矿地球化学角度深入研究了闪长质岩浆（岩）对两类铜矿床成矿物质来源的贡献，从而确定了月山地区成岩-成矿作用的内在联系，评价了岩浆岩体的成矿潜力。     

层控矿床的成岩成矿

本文从成岩分异,成岩交代,自生、脱水、泄水、压实、挤压、扩散和胶结作用等方面,论述层控矿床的成岩成矿作用。     

再论永梅会矿集区的找矿方向

永梅会矿集区具有独特的成矿地质背景，有望成为华南又一个以Cu为主的矿业基地。为实现这一国家目标．力争使矿产储量有较大幅度的增长，这就要求地质科学研究从战略与战术上紧密配合。在新一轮矿产资源调查中，拓宽找矿思路，明确找矿主攻目标。为此，提出四点建议：1．大胆探索找寻第二个紫金山式浅成低温热液型Cu、An矿床；2．拓展视域找寻浅埋、品位均一的斑岩型Cu（Au、Mo）矿床；3．找寻层位稳定的层控型复成因Cu多金属矿床；4．找寻其他新的矿床类型，诸如钱成高温型Sn、Cu矿床；与早侏罗世火山沉积岩盆地内层位性复成因矿床和火山岩盆地边缘或剥蚀残留火山岩盆地之下的基底地层内矿床。     

元素地球化学不活动组分判别——以库布苏金矿中矿带研究为例

本文从探讨元素不活动组分的原理出发 ,利用Gresens(196 7)质量平衡方程及Brimhall等 (1987)提出的元素不活动组分ΔX -fv 图解 ,对复杂热液成矿体系的元素不活动组分进行了深入探讨。指出了复杂体系内部各个子体系间元素不活动组分及体积变化上的差异。并结合实际 ,对库布苏金矿中矿带元素不活动组分进行了研究。同时对一些矿床地质现象的形成及成矿物质来源从元素地球化学角度进行了解释和判断。     

论岩浆的逆向演化及其成矿作用

长江中下游的岩浆岩在某些地区表现为由酸性→中性→基性的演化顺序,我们称之为岩浆的逆向演化.本文讨论了岩浆逆向演化的地质、地球化学背景及其产生机制,同时也论证了岩浆逆向演化与内生成矿作用的关系.