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地聚物胶凝材料能够替代水泥基胶凝材料作为固化剂应用于狭窄肥槽回填等工程问题中,有效降低水泥生产过程中的污染及能耗,但目前对于流态地聚物固化土胶凝材料的研究较少。采用3种新型绿色胶凝材料联合碱激发剂固化工程渣土形成流态地聚物固化土,通过对比其无侧限抗压强度,探究每种胶凝材料对于固化土强度特性的影响,同时建立强度预测模型,分析不同因素对于强度的影响程度。研究结果表明：固化土的强度随着碱激发剂模数的增加先提高后降低;固化土强度随着高炉矿渣（GGBS）、粉煤灰、稻壳灰掺量的增加均呈上升趋势,随着稻壳灰粒径的增长呈下降趋势;碱激发剂模数增至1.2、GGBS掺量增至10%、粉煤灰掺量增至8%和稻壳灰掺量增至11%时,固化土强度提升最为显著;强度预测模型预测结果的平均相对误差仅为5.57%,预测结果较为精准;预测模型中各层权值的计算结果表明养护龄期对于固化土强度影响最大,稻壳灰粒径影响程度最小。研究结果可以为固化土在实际工程的应用提供理论支持。 相似文献
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矿渣胶凝材料固化软土的力学性状及机制 总被引：4，自引：0，他引：4
利用矿渣胶凝材料固化软土,既可利用工业废渣,又能减少水泥的用量。以矿渣胶凝材料固化黏土、砂土二种软土。发现矿渣胶凝材料加固软土的效果远好于水泥、石灰,其9 %掺量的固化土28 d的无侧限强度达到2.0 MPa以上,普遍高于15 %掺量的水泥固化土,且其28 d固化土的软化系数普遍高于90 %以上,固化黏土后CBR值远高于同掺量的石灰固化土。X衍射结构分析表明,矿渣胶凝材料水化时产生的高强难溶的矿物晶体是其固化软土效果好的主要原因。因此,矿渣胶凝材料是一种性能优异的软土加固材料。 相似文献
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湖泊底泥改性固化的强度特性和微观结构 总被引：1，自引：0，他引：1
将灰渣胶凝材料作为改性剂应用于湖泊环境疏浚底泥的固化处理,研究了改性淤泥的强度特性,探讨灰渣胶凝材料对淤泥的改性机理。改性淤泥的抗压强度试验结果表明,当灰渣胶凝材料质量掺入比为5 %时,能够显著提高改性淤泥的各个龄期强度;当掺入质量比为12.5 %时,28天强度可以达到1.55 MPa。改性淤泥的早期强度较高,后期强度能持续增长,同时具有良好的耐水浸泡性能。SEM分析表明,灰渣胶凝材料能与底泥颗粒中的活性物质发生火山灰反应,形成高强难溶的胶结物,使改性淤泥中大孔隙数量减少,改善了淤泥土颗粒之间的胶结性能。这说明灰渣胶凝材料是一种性能优异的底泥改性材料。 相似文献
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分析丁木素类化灌材料的胶凝机理，并对硫木素、糠脲木素、酚醛木素等化灌材料进行了探索研究，给出了这几种浆材的配方、抗压强度、胶凝时间等参数，并分析了其影响因素。 相似文献
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聚氨酯是一种高聚物,可以通过填充孔隙、胶结土颗粒的作用达到提高强度和整体性的目的。采用聚氨酯对海砂进行固化处理,设计无侧限抗压强度试验和三轴剪切试验,分析不同胶凝时间和不同固化剂含量下固化海砂的强度特性和变形特性。试验结果表明,随着胶凝时间的增加,固化海砂的强度提高,在固化时间3 h时就可达到稳定强度的80%以上,并且在试验所采取的质量比范围内,质量比越高,固化效果越好;聚氨酯泡沫填充到孔隙中使颗粒之间的咬合力增大,增强了黏聚力;颗粒重排列的阻力增大,使得海砂抵抗变形的能力增加,峰值强度提高,静力特性发生明显变化。 相似文献
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本文结合镁质胶凝材料方面的一些实验资料,从热力学角度讨论了MgO+SiO_2蒸发生成滑石、纤维蛇纹石;白云石的滑石化、纤维蛇纹石化和白云石与滑石间的相互转变。提出以白云石代替MgO作合成生产镁质胶凝材料更加经济。 相似文献
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固化疏浚淤泥作为堤防填筑材料,既解决淤泥的处置,又可解决堤防建设中填土的缺乏。用灰渣胶凝材料（HAS）固化淤泥并测试固化淤泥土的主要物理力学性质,发现掺6 %灰渣胶凝材料固化后的淤泥土,在自然堆积28 d后的液塑限达到60 %,有机质含量降低到2 %,淤泥由原来的有机质高液限黏土（CHO）变成高液限粉质黏土（MH）,其28 d的无侧限抗压强度普遍大于1.4 MPa,凝聚力c≥100 kPa,内摩擦角?＞35°,渗透系数小于10-6 cm/s,远高于提防填筑材料的标准,表明灰渣胶凝材料固化改性淤泥成为堤防填土是可行的。 相似文献
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有机质干扰是困扰森林沼泽景观区化探工作多年的问题。对有机质对元素表生地球化学特征的影响机制进行了初步研究,结果表明:有机质主要通过直接吸附元素和改变环境的物理化学条件这两种方式对元素表生地球化学特征产生影响,两者之间又存在着密切的关系。研究结果较好地解释了由于有机质的干扰而使化探异常发生的变化。 相似文献
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Jane C. Shearer Timothy A. Moore Thomas D. Demchuk 《International Journal of Coal Geology》1995,28(2-4)
Floral character in mires has changed progressively through time. In the Carboniferous, pteridophytes, sphenophytes and lycophytes were dominant but by the Permian gymnosperms were an important component of mire flora. During the early Mesozoic gymnosperms remained the characteristic mire vegetation, together with pteridophytes, and conifers became dominant during the Jurassic. Cretaceous and Paleocene vegetation are similar, with taxodiaceous flora being important in mire vegetation. From the Eocene onwards, however, angiosperms were increasingly dominant in mire communities and in the Miocene herbaceous vegetation began to play a significant role. Together with these changes in floral character at least three aspects of coal character also appear to vary sequentially with time and are distinctive in the Tertiary: (1) proportions and thickness of vitrain banding, (2) coal bed thickness and (3) proportions of carbonised material. A compilation has been made of data from the coal literature comparing older coals with those of the Tertiary, in order to give a perspective in which to examine Tertiary coals. It was found that only Tertiary coals contain significant proportions of coal devoid of vitrain bands. In addition, Tertiary coals are the thickest recorded coal beds and generally contain low percentages of carbonised material (many less than 5%) as compared to older coals. It is interesting to note that Paleocene coal beds are similar to Cretaceous coals in that they tend to be thinner and contain higher proportions of carbonised material than do younger Tertiary coals.The absence of vitrain bands in some Tertiary coal beds is thought to result from the floras dominated by angiosperms, which are relatively easily degraded as compared to gymnosperms. The thickness of Tertiary coals may be related to an increase in biomass production from the Carboniferous through to the Tertiary, as plants made less investment in producing lignin, an energy-intensive process. In addition, with less lignin in plants, easier degradation of biomass may have facilitated nutrient recycling which, in turn, led to greater biomass production. Increased biomass production may have also ‘diluted’ the carbonised material present in some Tertiary peats, leading to lower proportions in the coal. Another possible cause of decreased carbonised components in Tertiary coal is that decreasing lignin content resulted in decreased charring during fires, as lignin is particularly prone to charring. A third possibility is that the carbonised component of peat may be concentrated during coalification so that Tertiary coals, generally of lower rank than Mesozoic or Paleozoic coals, contain a smaller fraction of carbonised plant material. It is not at present clear which of these mechanisms may have affected carbonised material in peat and coal but it is clear that lignin type and content has had an important role in determining peat and coal character since the Paleozoic. 相似文献
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文章阐述了碳酸盐岩的形成演化不仅与生物进化相关,而且对于环境水中的重金属和氟的迁移有抑制作用,探讨其在改善水质量、防治地方病以及调节或平衡土壤和植物元素的浓度比等方面的作用具有重大意义。研究指出,碳酸盐岩有利于形成适合于生命活动的地质环境,其作为中药材,碳酸盐矿物是自然界分布最为广泛的生物无机矿物,含有人体所需的常量元素、多种微量元素、有机质和HCO3-等成分,因而具有药用和营养价值。同时指出,不同碳酸盐岩药材成分的种类、含量及赋存状态等方面的差异导致其性味和归经不同。因而碳酸盐岩药物对人体的药效还与其入药形式、人体内的环境特点,尤其是不同成分之间在体内的协同作用与拮抗作用有关。因此,碳酸盐岩的药理作用是其所有成分与人体介质综合作用的结果。研究认为,只有加强碳酸盐矿物在地质环境的演化特点、化学成分、结构的微观分析以及理论药理的综合研究,才有利于认识碳酸盐岩的生物价值。 相似文献
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T. Spietz T. Chwoła A. Krótki A. Tatarczuk L. Więcław-Solny A. Wilk 《International Journal of Environmental Science and Technology》2018,15(5):1085-1092
Amine post-combustion carbon capture technology is based on washing the flue gas with a solvent that captures CO2. Thus, a small fraction of this solvent can be released together with the cleaned flue gas. This release may cause environmental concerns, both directly and indirectly through subsequent solvent degradation into other substances in the atmosphere. The paper presents the ammonia emission from CO2 capture pilot plant (1 tonne CO2 per day) using 40 wt% aminoethylethanolamine solvent, along with the efficiency of the water wash unit. In addition, the temperature effect of lean amine entering the absorber on ammonia emission was studied. Furthermore, the concentrations of other compounds such as SO2, SO3, NO2, CS2 and formaldehyde were monitored. The literature review on the NH3 emission from a pilot plant using aminoethylethanolamine solvent has not been published. The results show that the main source of ammonia emission is the absorber and that emission (in the range 27–50 ppm) corresponds to typical NH3 release from CO2 capture pilot plant using an amine solvent. The emission of amines and amine degradation products is a complex phenomenon which is difficult to predict in novel solvents, and for this reason the significance of new solvents testing in a pilot scale has been highlighted. 相似文献
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The effect of biomolecules on the mechanisms of the formation and nature of the transformation products of Al (oxy)hydroxides at the atomic and molecular levels and the impact on their nano-scale surface chemistry remain to be uncovered. In this article, the coordination structure of Al in Al (oxy)hydroxides formed under the influence of tannic acid was studied with X-ray absorption near edge structure (XANES) spectroscopy. Al K-edge and L-edge spectra show that as the tannate/Al molar ratio (MR) was increased from 0, 0.001, 0.01 to 0.1, the coordination number of Al changed from the sixfold coordination to mixed six-, five-, and/or fourfold coordination in the structural network of the Al (oxy)hydroxides formed under the increasing perturbation of tannic acid. In O K-edge spectra, the intensity of the peak assigned to the π∗ at 532.1 eV increased as the tannate/Al MR increased, with the spectrum of the Al precipitate formed at a tannate/Al MR of 0.1 being almost identical to that of tannic acid. These results indicate that tannate ligands are incorporated into the structural network of short-range ordered Al (oxy)hydroxides to perturb their structural configuration during the formation of Al precipitates under the influence of tannic acid. With increasing tannate/Al MR, the Al (oxy)hydroxides decreased in amount and developed structural defects and the Al-tannate precipitates increased in amount. The decrease in the coordination number of Al in the Al (oxy)hydroxides is attributed to steric and electronic factors which cause the change in Al-O bonding, because Al is complexed with tannate which has different functional groups and is much larger in size compared with OH and H2O ligands. The surface reactivity of a metal-O bond is related to its covalency and coordination geometry. The findings obtained in the present study are, thus, of fundamental significance in understanding the structural and surface chemistry of Al (oxy)hydroxides and their impact on the transformation, transport, and fate of nutrients and pollutions in the environment. 相似文献
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Although the relative length of digit impressions is often adopted as a binding character in ichnotaxa discrimination and trackmaker identification, it cannot be considered unequivocally operative. The reliability of this character has been evaluated by means of principal component analysis on several well‐preserved footprints (both manus and pes) referred to as Ichniotherium sphaerodactylum from the Early Permian Tambach Formation (Thuringia, Germany). The analysis reveals a substantial variability of digit impression length (especially in the manus), relativizing the validity of digit IV length as a diagnostic character as practised in different ichnological studies. Regarding the use of such a character, results clearly suggest the need to preliminarily conduct explorative analysis on the whole available ichnological material in order to detect which digit is the most consistent from an ichnotaxonomical standpoint, thus avoiding an arbitrary selection. Such a preliminary analysis should provide a better control on ichnotaxonomical splitting/lumping, particularly in the case of allied footprints, and can also be considered a valuable tool, if associated to functionality analysis, in improving and refining trackmaker identification. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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A rapid and simple method of analysis of silicate rocks using gold crucibles and fluoroboric acid as a solvent of the disintegrated material has been developed. The main elements are determined in a single treatment. The results obtained are comparable to the values recommended for samples of eleven standard rocks. 相似文献
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