LISBP, Université de Toulouse, CNRS, INRA, INSA, Toulouse, France.
LISBP, Université de Toulouse, CNRS, INRA, INSA, Toulouse, France.
Water Res. 2017 Dec 1;126:399-410. doi: 10.1016/j.watres.2017.09.051. Epub 2017 Sep 28.
The treatment of nanoparticle (NP) polluted aqueous suspensions by flotation can be problematic due to the low probability of collision between particles and bubbles. To overcome this limitation, the present work focuses on developing an enhanced flotation technique using the surface-functionalized microbubbles - colloidal gas aphrons (CGAs). The CGA generator was adapted to be air flow rate controlled based on the classical Sebba system; thus it could be well adopted in a continuous flotation process. Cetyl trimethylammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) were employed for CGA creation. Positively surface-charged CTAB-CGAs (∼44.1 μm in size) and negatively surface-charged SDS-CGAs (∼42.1 μm in size) were produced at the optimum stirring speed of 8000 rpm. The half-life of CGAs varied from 100 s to 340 s under the tested conditions, which was largely sufficient for transferring CGAs from bubble generator to flotation cell. The air flow led to less stable CTAB-CGAs but apparently enhanced the stability of SDS-CGAs at higher air flow rates. In the presence of air flow, the drainage behavior was not much related to the type of surfactants. The continuous CGA-flotation trials highlighted the effective separation of silica nanoparticles - the removal efficiencies of different types of SiO NPs could reach approximately 90%-99%; however, at equivalent surfactant concentrations, no greater than 58% of NPs were removed when surfactants and bubbles were separately added into the flotation cell. The SiO NPs with small size were removed more efficiently by the CGA-flotation process. For the flotation with CTAB-CGAs, the neutral and basic initial SNP suspension was recommended, whereas the SDS-CGAs remained high flotation efficiency over all investigated pH. The good performance of CGA-flotation might be interpreted: most of the surfactant molecules well covered/coated on the surfaces of stable CGAs and thus fully contacted with NPs, resulting in the efficient utilization of surfactants.
纳米颗粒 (NP) 污染水悬浮液的浮选处理可能存在问题,因为颗粒与气泡之间碰撞的概率较低。为克服这一限制,本工作重点开发了一种使用表面功能化微泡-胶体气穴(CGA)的强化浮选技术。CGA 发生器根据经典 Sebba 系统进行了空气流量控制的适配,因此可以很好地应用于连续浮选过程。十六烷基三甲基溴化铵(CTAB)和十二烷基硫酸钠(SDS)用于 CGA 的制备。在最佳搅拌速度为 8000rpm 时,制备出带正电荷的 CTAB-CGA(尺寸约为 44.1μm)和带负电荷的 SDS-CGA(尺寸约为 42.1μm)。在测试条件下,CGA 的半衰期从 100s 到 340s 不等,这对于将 CGA 从气泡发生器转移到浮选槽来说已经足够长了。在空气流量的作用下,CTAB-CGA 的稳定性降低,但在较高的空气流量下,SDS-CGA 的稳定性明显增强。在空气流量存在的情况下,排水行为与表面活性剂的类型关系不大。连续的 CGA 浮选试验突出了硅纳米颗粒的有效分离-不同类型的 SiO NPs 的去除效率可达 90%-99%左右;然而,在等效表面活性剂浓度下,当表面活性剂和气泡分别添加到浮选槽中时,去除的 NPs 不超过 58%。CGA 浮选过程更有效地去除小尺寸的 SiO NPs。对于 CTAB-CGA 浮选,推荐使用中性和碱性初始 SNP 悬浮液,而 SDS-CGA 在所有研究的 pH 值下仍保持较高的浮选效率。CGA 浮选性能良好的原因可能是:大多数表面活性剂分子很好地覆盖/涂覆在稳定 CGA 的表面上,并与 NPs 充分接触,从而有效地利用了表面活性剂。