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利用SiO2-Al2 O3-CaO-FeOx 四元体系研究了煤中矿物质热和黏温特性规律。利用热机械分析、差热、X射线衍射和热力学模拟以及高温旋转黏度计分析了矿物质的高温演化、反应和黏温特性(1700℃到固化温度)。结果表明，热机械分析和差热可以较好地在线考察矿物质高温特性。二氧化硅和氧化铝从低温矿物转变成高温形态，表现出稳定的结构和高黏度；另一方面，加入氧化钙或氧化铁可以起到助熔剂的作用，显著加快二氧化硅和氧化铝的反应和转化并降低黏度。氧化亚铁相比氧化铁和四氧化三铁表现出更明显的降低黏度的作用，而氧化铁还原成金属将显著提高体系黏度。三价铁离子与铝类似，可构成网架结构。另外，氧化铁在弱还原或高温下将产生部分二价铁离子对网架机构进行调整。氧化钙的存在可以加强四元体系中氧化铁的溶解能力，进而降低黏度。“,”In the present work, the synergistic effect of components on the mineral behavior in the SiO2-Al2 O3-CaO-FeOx quaternary system was tentatively evaluated. The mineral transformation and reaction were analyzed by thermo-mechanical analyzer ( TMA ) , differential scanning calorimetry ( DSC ) , X-ray diffraction ( XRD ) and thermodynamic calculation ( FactSage ) . In addition, the apparent viscosities of synthetic slags, expressed as a function of temperature and composition, were determined using a high temperature rotary viscometer with temperature ranging from 1 700℃ to re-solidifying temperature. The results demonstrated that the TMA and DSC approaches were applicable to characterize the mineral behavior under in-situ conditions. Silica and alumina preferred to be transformed to high temperature cristobalite and a-alumina with relatively stable structure and high viscosity, respectively. On the other hand, the reaction and transformation of silica and alumina could be accelerated by some valuable fluxing agents, particularly calcium oxide and iron oxides. The addition of ferrous oxide into synthetic slags could lower its viscosity compared with that of ferric oxide and ferroferric oxide. Furthermore, the reduction of iron oxides to metallic iron remarkably increased the viscosity. Ferric oxide may take part in the random glass network in a similar fashion with alumina. Besides, iron oxides with the oxidation state of Fe2+may also act as a modifier under slightly reducing conditions and higher temperatures. The sensitivity of viscosity of mineral matters to temperature excursion decreased with increasing calcium oxide content as calcium oxide was able to enhance the solution ability of iron oxides in the SiO2-Al2 O3-CaO-FeOx quaternary system.