基于热重分析的菱镁矿分解动力学解析

本文利用热重(TG)分析方法,探讨了菱镁矿的热分解过程。根据热微商(DTG)曲线峰顶温度,结合Kissinger及Ozawa-Doyle方法拟合计算得到菱镁矿热分解的活化能和指前因子(lgA)分别为211.55 kJ/mol和11.07s-1。依次采用单曲线拟合、多元非线性拟合及Malek方法判定得出菱镁矿热分解过程属于三维相界反应模型(R3),其动力学方程为:dα/d T=(1011.07/β)·e-211.55×103/(8.314×T)·3(1-α)2/3。     

A Novel Concept for the Removal of Solvent Vapors from Exhaust Air

The emission of large amounts of solvent vapors with exhaust air from industrial production into the environment is a serious problem. In Germany, industry‐sector‐specific threshold values are applied and technical measures for pollution reduction are required. Different techniques for exhaust air cleaning are in use but still posing problems concerning costs and reliability. For these reasons, the development of processes for exhaust air treatment is the subject of the current research. A new concept for exhaust air cleaning is introduced that combines absorption of a solvent vapor by an organic fluid and a subsequent adsorption by a molecular sieve placed in the absorber. It was managed to close the loops of solvent recovery and sorbents regeneration. In laboratory‐scale experiments it was possible to reduce an initial ethylacetate pollution of 800 mg/m³ or 349 mg C/m³ below the limit value of 75 mg C/m³ over 60 h duration. Thermogravimetric measurements assisted to define optimum conditions for solvent recovery at 180°C from the molecular sieve. One unexpected positive finding was the considerable increase in the solvent release in the presence of the absorption fluid while adsorption isotherms revealed first insight into this process.     

矿物热分解动力学的研究方法探讨

:矿物分解动力学的研究可以大大提高我们对地质作用过程中矿物生长、元素和流体迁移等过程的了解。本文在介绍固相反应动力学原理的基础上 ,讨论了常压下研究矿物分解动力学的热重分析法和电导率法 ,指出精确确定高压下的反应分数 ,是研究高压下矿物热分解动力学的关键。提出了高压下确定反应分数的方法。     

基于模糊综合评判的煤自燃发火倾向性研究

自燃发火倾向性是煤自燃火灾的主要影响因素之一。通过对国内外煤自燃倾向性鉴定方法的分析, 指出了我国现行的煤自燃倾向性的不足之处。根据煤自燃机理的煤、氧复合理论,建立了依据煤在低温氧化过程中的吸氧率、放热强度和着火燃烧阶段的活化能作为鉴定煤自燃发火倾向性影响因素的模糊综合评判新方法。在此基础上,用热重分析方法测试了5种煤样在相同条件的指标参数,建立模糊综合评判模型,通过模糊运算得出评判5种煤样自燃发火倾向性的综合指标。验证表明,该方法有较强的实用性,其评判结果与5种煤样的实际自燃发火期趋势一致。      

铁矿石灼烧减量测试新方法——热重分析法

采用热重分析法(TGA)测量铁矿石样品灼烧减量,对保温时间、加热温度、加热速率和工作气氛等工作条件进行了系统研究,确立TGA法适宜的工作条件为:20℃/m in加热至1 000℃,保温30 min,全程选用高纯氮为工作气体。对多种进口铁矿石样品采用TGA法和常规马弗炉加热法进行测量,对比结果表明,TGA法具有方便快捷、准确可靠、适用范围宽、样品消耗量小等优点,且可以清楚监控样品失重全过程,为铁矿石挥发分的成分分析提供有力的数据参考。     

Chemical Characterisation of Geological Raw Materials Used in Traditional Ceramics

A wide range of natural raw materials is used in the manufacture of traditional ceramic products such as ceramic tiles, frits, glazes and pigments. The chemical composition of these raw materials needs to be strictly controlled to assure end-product quality and enable the identification of the origin of defects caused by impurities or contamination. Six types of ceramic raw materials (silica sand, clays and kaolin, feldspars and related minerals, calcium and magnesium carbonates, sodium and calcium borates, and zirconium silicates) have been analysed in this study. X-ray fluorescence (XRF), potentiometry, coulometry and atomic absorption spectrometry (AAS) were used in this chemical characterisation. A methodology has been established for characterising each studied raw material, by identifying the chemical elements to be determined, selecting the most appropriate technique and validating each measurement. The reference materials used for validation were BCS CRM 267, 313/1, 393 and 388 (BAS), GBW 03103, GBW 07404, NIST SRM 181, 201a and 1835, Euronorm CRM 782-1 and Syenite SY-2. The results showed that most of the elements present in the geological samples used as traditional ceramic raw materials could be determined by XRF. The determination of light elements, such as lithium, fluorine and boron, is more suitably conducted by ICP-AES/AAS, potentiometry or potentiometry/ICP-AES respectively. Organic and inorganic carbon could be determined by coulometry. Inorganic carbon (CO₂) could also be determined by coulometry or by thermogravimetry, if samples did not contain clay minerals. Loss on ignition was always determined by gravimetry.     

Thermal characterization of natural and synthetic humic substances

Thermogravimetric technique was used for the characterization of natural (humic) and synthetic (melanoidins) substances. The influence of pH on the thermal stability of humic substances was studied. A similarity in thermal behaviour of natural humic substances and of melanoidins (prepared from an excess of sugar) and the unique thermal properties of melanoidins (prepared from basic amino acids) was observed. Thermal behavior of natural and synthetic substances was compared with model compounds of sugar, peptide and kerogen types.     

阳离子交换容量和烷基链链数对有机蒙脱石性能的影响

已有研究表明影响有机蒙脱石性能的因素很多,除了有机改性剂的特性外,蒙脱石的晶体化学特征也是不容忽视的因素。为了探讨烷基链链数和阳离子交换容量与有机蒙脱石性能之间的关系,本文选择3种不同阳离子交换容量的蒙脱石为主体,4种季铵盐阳离子改性剂十八烷基三甲基溴化铵(S18)、双-十八烷基二甲基溴化铵(D18)、十二烷基三甲基溴化铵(S12)和双-十二烷基二甲基溴化铵(D12)为客体,在不同添加量条件下(0.2、0.5、1.0、1.5、2.0、2.5、3.0、4.0CEC)制备了多个系列的有机蒙脱石,并用XRD、TG-DTG等手段对产物进行表征。实验结果表明,阳离子交换容量与层间柱撑高度之间不存在明显的相关性,但对表面活性剂在蒙脱石上的吸附量有显著的影响,吸附量随着阳离子交换容量的增加而增加。双链表面活性剂对蒙脱石层的撑开能力比单链更强,在层间具有更复杂的自组装过程,导致其热分解过程更为复杂。     

真空抽提结合同位素分析技术研究风化剖面中水的氢氧同位素组成特征

沉积物不同赋存态水作为地球表生过程水岩相互作用的产物,其氢氧同位素组成对于探讨古气候、古环境演变有重要的意义。本文采用热重-真空抽提-液态水同位素测试三者联立技术,提取湖南风化剖面样品不同赋存态水,并测试其氢氧同位素组成。热重分析确立4段抽提温度区间:0~120℃、120~300℃、300~600℃和600~900℃;除120~300℃及300~600℃抽提出的赋存态水性质无法确定外,其余2个温度段赋存态水分别对应吸附水和结构水;0~120℃提取的吸附水主要为现代大气降水的蒸发残余水。由于同位素平衡分馏的原因,赋存态水与矿物晶格结合越紧密,其氢同位素值越偏负,氧同位素值越偏正。本研究方法可为地球表生过程和水循环研究提供依据。