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用于正向渗透汲取液的聚丙烯酸钠(PSA)包覆磁性纳米颗粒的合成

Synthesis of Poly-Sodium-Acrylate (PSA)-Coated Magnetic Nanoparticles for Use in Forward Osmosis Draw Solutions.

作者信息

Ban Irena, Markuš Sabina, Gyergyek Sašo, Drofenik Miha, Korenak Jasmina, Helix-Nielsen Claus, Petrinić Irena

机构信息

Faculty of Chemistry and Chemical Engineering, University of Maribor, Smetanova ulica 17, SI-2000 Maribor, Slovenia.

Department for Materials Synthesis, Jožef Stefan Institute, SI-1000 Ljubljana, Slovenia.

出版信息

Nanomaterials (Basel). 2019 Aug 31;9(9):1238. doi: 10.3390/nano9091238.

Abstract

The synthesis of magnetic nanoparticles (MNPs) coated with hydrophilic poly-sodium-acrylate (PSA) ligands was studied to assess PSA-MNP complexes as draw solution (DS) solutes in forward osmosis (FO). For MNP-based DS, the surface modification and the size of the MNPs are two crucial factors to achieve a high osmolality. Superparamagnetic nanoparticles (NP) with functional groups attached may represent the ideal DS where chemical modifications of the NPs can be used in optimizing the DS osmolality and the magnetic properties allows for efficient recovery (DS re-concentration) using an external magnetic field. In this study MNPs with diameters of 4 nm have been prepared by controlled chemical co-precipitation of magnetite phase from aqueous solutions containing suitable salts of Fe and Fe under inert atmosphere and a pure magnetite phase could be verified by X-ray diffraction. Magnetic colloid suspensions containing PSA-coated MNPs with three different molar ratios of PSA:MNP = 1:1, 1:2 and 1:3 were prepared and assessed in terms of osmotic pressure, aggregation propensity and magnetization. Fourier Transform Infrared Spectroscopy (FTIR) confirmed the presence of PSA on coated MNPs and pristine PSA-MNPs with a molar ratio PSA:MNP = 1:1 exhibited an osmotic pressure of 30 bar. Molar ratios of PSA:MNP = 1:2 and 1:3 lead to the formation of less stabile magnetic colloid solutions, which led to the formation of aggregates with larger average hydrodynamic sizes and modest osmotic pressures (5.5 bar and 0.2 bar, respectively). After purification with ultrafiltration, the 1:1 nanoparticles exhibited an osmotic pressure of 9 bar with no aggregation and a sufficient magnetization of 25 emu/g to allow for DS regeneration using an external magnetic field. However, it was observed that the amount of PSA molecules attached to the MNPs decreased during DS recycling steps, leaving only strong chelate-bonded core-shell PSA as coating on the MNPs. This demonstrates the crucial role of MNP coating robustness in designing an efficient MNP-based DS for FO.

摘要

研究了包覆亲水性聚丙烯酸钠(PSA)配体的磁性纳米颗粒(MNP)的合成,以评估PSA-MNP复合物作为正向渗透(FO)中汲取溶液(DS)溶质的性能。对于基于MNP的DS,MNP的表面改性和尺寸是实现高渗透压的两个关键因素。带有官能团的超顺磁性纳米颗粒(NP)可能代表理想的DS,其中NP的化学修饰可用于优化DS渗透压,并且磁性特性允许使用外部磁场进行高效回收(DS再浓缩)。在本研究中,通过在惰性气氛下从含有合适的铁盐和亚铁盐的水溶液中控制化学共沉淀磁铁矿相来制备直径为4nm的MNP,并且可以通过X射线衍射验证纯磁铁矿相。制备了含有PSA包覆的MNP的磁性胶体悬浮液,其中PSA与MNP的摩尔比为三种不同比例:1:1、1:2和1:3,并对其渗透压、聚集倾向和磁化强度进行了评估。傅里叶变换红外光谱(FTIR)证实了包覆的MNP上存在PSA,摩尔比为PSA:MNP = 1:1的原始PSA-MNP表现出30 bar的渗透压。PSA:MNP = 1:2和1:3的摩尔比导致形成稳定性较差的磁性胶体溶液,这导致形成平均流体动力学尺寸较大且渗透压适中的聚集体(分别为5.5 bar和0.2 bar)。用超滤纯化后,1:1的纳米颗粒表现出9 bar的渗透压,无聚集,并且具有25 emu/g的足够磁化强度,以允许使用外部磁场进行DS再生。然而,观察到在DS循环步骤中附着在MNP上的PSA分子数量减少,仅留下强螯合键合的核壳PSA作为MNP上的涂层。这证明了MNP涂层坚固性在设计用于FO的高效基于MNP的DS中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/754b/6781102/2e592e527724/nanomaterials-09-01238-g001.jpg

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