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Ultrafine Particle Recovery Using Thin Permeable Films

机译:使用薄透膜的超细颗粒回收

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摘要

The selective recovery of ultrafine, <10 μm, particles remains a significant challenge in the minerals industry. Indeed, these particles often report to tailings impoundments, resulting in under-utilization of mined resources and the need for tailings dams. Recently, a technique has been developed offering the potential to selectively recover particles down to <1 μm in size. This technique, originally inspired by oil agglomeration, uses a high internal-phase water in oil emulsion as a binder to selectively agglomerate hydrophobic particles. Due to the significant concentration of the dispersed aqueous phase, ~95%, the continuous organic phase forms a network of very thin, permeable films, estimated to be 60 nm thick. These are stabilized by an emulsifier. In the high shear field of the agglomeration process, the binder is fragmented into smaller hydrophobic portions, delivering its thin film coating to the adhering hydrophobic particles. Permeation of water across the thin films eliminates the viscous hydrodynamic resistance, permitting sub-micron particle recovery to occur at rates similar to those for particles considerably larger in size. This recovery occurs within seconds under intense mixing. In this study, a model system consisting of magnetite, with a Sauter mean diameter of 11.4 μm, was agglomerated using the water in oil emulsion binder. The binder, which contained the emulsifier sorbitan monooleate, appeared to also act as a collector for the magnetite, thus no separate particle conditioning step was required. Curiously, however, the binder requirements were higher than expected. Further investigations concerning the stability of the binder revealed that the magnetite particles were causing rapid binder degradation. Therefore, prior to agglomeration using the binder, the particles were conditioned with sorbitan monooleate to render them hydrophobic. This pre-conditioning led to significant reductions in the binder dosage required to achieve agglomeration. Moreover, the resulting dosage matched that predicted by a model silica system for the same specific hydrophobic surface area, thus allowing a model to be validated based on the required binder dosage for a known hydrophobic surface area. Examination of binder stability in the presence of conditioned magnetite revealed that the now hydrophobic particles stabilized the binder.
机译:<10μm的超细颗粒的选择性回收仍然是矿物工业中的重大挑战。确实,这些颗粒经常报告给尾矿库,导致开采资源的利用不足以及对尾矿坝的需求。近来,已经开发出一种技术,该技术提供了选择性地回收尺寸小于1微米的颗粒的潜力。该技术最初是受油团聚的启发,它使用高内相油包水乳液作为粘合剂来选择性地凝聚疏水性颗粒。由于分散的水相的浓度很高(约95%),连续的有机相形成了非常薄的可渗透膜网络,估计厚度为60 nm。这些通过乳化剂稳定。在附聚过程的高剪切场中,粘合剂会破碎成较小的疏水部分,从而将其薄膜涂层输送到粘附的疏水颗粒上。水在薄膜上的渗透消除了粘性的流体动力阻力,使亚微米级颗粒的回收率与大得多的颗粒相似。在强烈混合下,这种恢复在几秒钟内发生。在这项研究中,使用油包水型乳液粘合剂将由Sauter平均直径为11.4μm的磁铁矿组成的模型系统团聚。包含乳化剂脱水山梨糖醇单油酸酯的粘合剂似乎也可作为磁铁矿的集电器,因此不需要单独的颗粒调节步骤。然而,奇怪的是,粘合剂的要求高于预期。关于粘合剂稳定性的进一步研究表明,磁铁矿颗粒导致粘合剂快速降解。因此,在使用粘合剂附聚之前,用脱水山梨糖醇单油酸酯调节颗粒以使其疏水。这种预处理可显着减少实现团聚所需的粘合剂剂量。此外,所得剂量与模型二氧化硅系统预测的相同比疏水表面积相匹配,因此可以基于已知疏水表面积所需的粘合剂剂量对模型进行验证。在条件磁铁矿的存在下对粘合剂稳定性的检查表明,现在的疏水性颗粒使粘合剂稳定。

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