Adsorption of aluminium by a latosol as affected by phosphate and glutamic acid

The effect of phosphate and glutamic acid on adsorption of aluminium onto a latosol was investigated as a function of pH and ligand concentrations through batch equilibrium experiments. The results showed that adsorption of aluminium by the soil was enhanced after addition of phosphate at low pH, and this promotive effect was gradually eliminated with the increase in pH. The positive effect of phosphate on aluminium adsorption onto latosol was attributed to phosphate-induced surface negative charge and formation of ternary surface complexes involving aluminium and phosphate. While using silica as adsorbent, the inactive surfaces for phosphate, promotion of adsorption of aluminium by phosphate was also found. Then it was proposed that additional aluminium might bind to the phosphate adsorbed onto the silica in the form of surface complexes silica–aluminium–phosphate again, and the mechanism might operate in the soil systems as well. Glutamic acid exhibited no influence on the adsorption of aluminium by the soil at low pH. After increasing the pH, adsorption of aluminium was inhibited especially with the highest addition of glutamic acid, probably owing to weak affinity of complexes between glutamic acid and aluminium to the soil.     

光催化降解乐果的动力学研究

采用30 W石英紫外灯作为光源,研究了乐果在二氧化钛悬浮体系中光催化降解反应的动力学规律。考察了乐果起始浓度、TiO2用量、溶液pH值及温度对乐果光催化降解速率的影响,结果表明,乐果光催化降解符合表观零级动力学规律。由于速率常数k与乐果起始浓度有关,表明乐果光催化降解反应不是一个简单的零级反应。     

A study on the adsorption of chromium on laterite from Guizhou Province,China

The adsorption behaviors of Cr(VI) on laterite from Guizhou Province were studied in this paper, and the adsorption mechanism was discussed as well. Results showed that different mineral compositions in the laterite would cause differences in the capacity of laterite to absorb Cr(VI). Gibbsite, iron oxide minerals and non-crystalloids are the main contributors to enhancing the capacity of laterite to absorb Cr(VI). The pH of the solution is an important factor affecting the adsorption of Cr(VI) on laterite. Acidic environment (pH=2–5) is favorable to the adsorption of Cr(VI). The amount of adsorbed Cr(VI) decreases with increasing pH of the solution. With increasing initial concentrations of Cr(VI), the amount of adsorbed Cr(VI) increases first, and then decreases. The optimal adsorption concentration of Cr(VI) on laterite is 250 μg/mL. The adsorption of Cr(VI) on laterite is a rapid process, about 80% Cr(VI) will be adsorbed within 2 hours. And the adsorption of Cr(VI) on kaolinite is a slow process.     

塔里木盆地库车坳陷中生界烃源岩生烃动力学参数研究

根据封闭体系黄金管热模拟实验结果,应用Kinetics专用软件,研究了塔里木盆地库车坳陷中生界不同类型烃源岩的生烃特征与动力学参数。库车坳陷侏罗系煤、碳质泥岩、泥岩及三叠系湖相泥岩具有各自的活化能分布和频率因子,揭示出其生烃行为的差异性。利用GOR-IsotopeKinetics软件,推导了库车坳陷侏罗系煤、泥岩和三叠系湖相泥岩3类烃源岩的碳同位素动力学参数。上述参数的获取,为盆地模拟、烃源岩评价、生烃量计算及资源量预测提供了重要的基础地球化学数据。      

Copper(II) humate mobility in kaolinite soil

An investigation of the influence of humate on the mobility of copper(II) ions in a kaolinite soil using leaching tests and electrokinetic experiments is reported. The data are interpreted in terms of humate–copper–clay interactions and humate electrical charge. Humate is mostly immobile below pH8 but is more mobile in alkaline conditions (sorption to kaolinite reduces its mobility in neutral conditions). Copper humate complexes are mobile in both acidic and alkaline conditions, but not in neutral conditions where they are sorbed. The dissolved copper humate complexes that form in acidic conditions are positively charged. The net effect of humate is to increase cupric ion mobility in kaolinite soil, especially in alkaline conditions.     

准噶尔盆地陆东-五彩湾石炭系烃源岩特征及生烃动力学研究

准噶尔盆地陆东-五彩湾地区石炭系具有良好的勘探前景,该地区石炭系烃源岩有机质丰度较高,成熟度范围宽,主要处于成熟-高成熟演化阶段,主要由Ⅲ型有机质组成。在对烃源岩样品进行常规评价的基础上,用开放体系进行了热解实验和动力学模拟,对陆东-五彩湾地区的生烃特征进行了研究,尝试了高成熟烃源岩生烃过程研究及Ⅲ型干酪根液态烃排烃时间的估计,并对石炭系地层产烃率进行了计算。结果显示,陆东-五彩湾地区石炭系最早在二叠纪（距今264 Ma左右）开始生烃,后期由于地层抬升,在古近纪早期（距今61 Ma左右）结束生烃。下石炭统产烃率大,液态烃排出时间估计在距今232~196 Ma之间;上石炭统产烃率较小,液态烃排出时间估计在距今196~178 Ma 之间,但天然气生成相对较晚,有利于天然气的保存。天然气可能主要来源于上石炭统烃源岩。     

A simulation experimental study on oxidative kinetics of sphalerite under hypergene condition

The sphalerite oxidative kinetics under hypergene condition was simulated and studied by means of a mixed flow reactor over a pH range of 1.0 7.8,and at dissolution temperatures from 20 to 55℃,ferric ion concentrations from 1.0×10-5 to 1.0×10-2 mol/L,O 2 flux of 0.5 L/min,and oxidants of ferric ion and O 2.It is indicated that with ferric ion as oxidant,the oxidation rate of sphalerite increases with increasing ferric ion concentration,temperature and decreasing pH value,and under the studied conditions,the dissolution rates of Zn and Cd are approximately identical,with the values of activation energy being 41.75 and 42.51 kJ·mol-1,respectively,suggesting that the oxidation rate of sphalerite is controlled by chemical reactions on mineral surface.However,with O 2 as oxidant,the oxidation mechanism of sphalerite varies with pH value.Oxidation rate decreases with increasing pH value when pH is lower than 5.95,whereas the increase of pH value results in an increase in oxidation rate when pH value is higher than 7.The oxidation rate of sphalerite can be expressed as:R Zn =10 1.1663 [Fe3+] 0 0.154 ·[H+] 0.2659 ·e-41.75/RT or R Cd =10 1.7292 [Fe3+] 0 0.170 ·[H+] 0.2637 ·e-42.51/RT     

β-环糊精交联聚合物对氯苯的吸附特性

通过对水中含有微量氯苯的吸附特性研究,考察β-环糊精交联聚合物吸附氯苯的动力学、热力学及连续运行条件下的稳定性和再生性能。实验结果表明:β-环糊精交联聚合物吸附氯苯的过程符合准二级动力学模型,即化学吸附是吸附过程的控制步骤;β-环糊精交联聚合物上的等温吸附符合Langmuir吸附等温模型。在15、25、35℃时最大吸附量分别为23.36、28.17、27.85mg/g;动态模拟实验中,当氯苯质量浓度为10mg/L时,氯苯的去除率大于80%。乙醇作为溶剂可以使吸附饱和的β-环糊精交联聚合物再生。     

Acid leaching of ash and coal: Time dependence and trace element occurrences

The leaching of coal and coal/asphaltite/wood-ashes in sulfuric acid (pH 1.0, 25 °C, S/L, 1:10) was studied as a function of time; acid consumption and extracted metal concentrations are presented. Whole coals consumed acid rapidly during the first few minutes, followed by slow acid consumption. Wood-, lignite-, and asphaltite-ashes consumed acid in two stages, the rapid phase extending < 30 min and the slow phase extended up to 10 days. The rapid phase was dominated by the dissolution of Ca, K and Mg ions for wood-ash, by Ca, Al and Mg ions for lignite-ash and Ca and Mg ions for asphaltite-ash. The sulfur concentration in solution and the concentrations of Ca, Fe, K, Mg, Na, P, Al and Mn in the aqueous phase verified the neutralizing capacity of the untreated ashes as well as the formation of insoluble sulfates in the residues. The slow phase kinetics differed for different fuels and exhibited leaching of several abundant elements—Fe, Al, K, Na and Mn. Trace elements (Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, Th, U, V, Zn) sometimes required up to 32 h for maximal extraction from ashes. Suggestions are presented regarding the chemical nature of trace elements in the untreated coals and ashes and suitable residence times for economical industrial processes. We think it possible to combine bacteriological oxidation of sulfidic concentrates of acid leaching from ash of various qualities or even whole coals.     

煤生烃动力学研究进展

化学反应动力学是评价煤的生烃过程和生烃特性行之有效的方法。目前,煤生烃动力学模型理论研究和标定得到了不断的深化,煤生烃动力学研究在认识煤源岩成烃规律方面也有长足发展,并在煤源岩评价中初见成效。但是在压力条件下,关于生烃动力学在煤源岩定量和动态评价方面的研究则报道较少。另外,对单体化合物形成动力学的研究还处于探索之中。这些研究将代表煤源岩生烃动力学领域未来发展的重要方向。