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首页> 外文期刊>European journal of mineralogy >Influence of gel-strength and magnesium doping on the organization of calcite/hydrogel mesocrystal composites
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Influence of gel-strength and magnesium doping on the organization of calcite/hydrogel mesocrystal composites

机译:凝胶强度和镁掺杂对方解石/水凝胶间晶体复合材料组织的影响

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Calcite growing in biomimetic hydrogel environments incorporates the gel during its growth. The amount of occluded gel within the composite is mainly determined by the interaction between gel strength and crystallization pressure, with the latter being directly related to supersaturation and growth rate. In previous work we established a direct correlation between increased amounts of occluded gel with misorientations in the growing calcite crystals or aggregates. The presence of Mg2+ in the growth environment adds complexity to the internal structuring of the mineral. In this contribution we examine the effects of Mg2+ on the mechanical parameters of gelatin hydrogel and silica hydrogel by mechanical shear stress tests, we determine characteristics of the gel fabric occluded in the calcite using selective etching techniques and high-resolution field emission scanning electron microscope (FE-SEM) imaging, and we use electron backscatter diffraction (EB SD) to study co-orientation or misorientation in the calcite crystals or aggregates. We show that two independent mechanisms are responsible for the complex impact of Mg2+ in the growth medium on the calcite/gel composites. First, addition of 0.1 M Mg2+ reduces the yield-strength of the gels by about 50%. While gelatin gel shows continuous strain hardening in a similar way for Mg-bearing and Mg-free systems, the silica-gel weakens after reaching an ultimate shear strength, where the strain associated with the maximum in strength shifts by 350% to higher values. The decreased gel strength in the Mg-bearing systems leads to decreased amounts of occluded gel. Second, incorporation of Mg2+ in the growing calcite (i) increases its solubility and thus decreases crystallization pressure, and (ii) introduces small angle grain boundaries due to misfit strains which lead to "split growth", i.e. misoriented subunits of the calcite or ultimately spherulitic growth. Our study further clearly shows that Mg not only influences the o
机译:仿生水凝胶环境中的方解石生长在其生长过程中含有凝胶。复合材料内的封闭凝胶的量主要由凝胶强度与结晶压力之间的相互作用决定,后者与过饱和和生长速率直接相关。在以前的工作中,我们在越来越多的方解石晶体或聚集体中,建立了增加的封闭凝胶量增加的堵塞凝胶的直接相关性。生长环境中Mg2 +的存在增加了矿物质内部结构的复杂性。在这一贡献中,我们通过机械剪切应力测试检查Mg2 +对明胶水凝胶和二氧化硅水凝胶的机械参数的影响,我们使用选择性蚀刻技术和高分辨率场发射扫描电子显微镜确定方解石中封闭的凝胶织物的特性( FE-SEM)成像,我们使用电子反向散射衍射(EB SD)研究方解石晶体或聚集体中的共同取向或杂散。我们表明,两个独立的机制负责Mg2 +在方解石/凝胶复合材料上的生长培养基中的复杂影响。首先,添加0.1M Mg2 +将凝胶的产率强降低约50%。虽然明胶凝胶以类似的方式显示连续应变硬化,但是在达到最终剪切强度后,二氧化硅 - 凝胶在达到最终剪切强度之后削弱,其中与强度最大的菌株将350%偏移到更高的值。 Mg轴承系统中的凝胶强度降低导致堵塞凝胶的量减少。其次,在生长方解石(I)中掺入Mg2 +增加其溶解度并因此降低结晶压力,并且(ii)由于错误的菌株引起了小角度晶界,这导致了“分裂生长”,即石材的无主管的亚基或最终嗜铬生长。我们的研究进一步清楚地表明MG不仅影响o

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