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Ion exchange and membranes最新文献

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Development of SIRA process for brackish water demineralization by ion exchange. 离子交换法脱盐微咸水SIRA工艺的研究进展。
Pub Date : 1975-12-01
G Boari, L Liberti, R Passino
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引用次数: 0
Editorial: Hazards in polymer chemistry. 社论:聚合物化学中的危害。
Pub Date : 1975-12-01
J Mikes
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引用次数: 0
Pore flow models and their applicability. 孔隙流动模型及其适用性。
Pub Date : 1975-12-01
M N Sarbolouki

Pore flow models are classified and concisely reviewed, and it is shown that despite their apparent differences, they are equivalent. It is proven that the difference between the classic formula of Guerout-Elford-Ferry and the most recent ones developed by Pappenheimer-Ussing and Kedem-Katchalsky, is due to the introduction of a more proper viscosity coefficient for the water inside the membranes in the newer formulae. Fundamental assumptions involved in the models are restated and criteria for their applicability are mentioned. Arguments regarding the fundamental validity of the pore size formulae when applied to tight membranes, where continum hydrodynamics become questionable, are reviewed. Recent theoretical analysis of the situtation by Mikulecky, where he shows the calculated pore size merely reflects the extent of the membrane-water interaction is briefly presented. It is argued that since his analysis neglects the influence of the membrane-water interaction on the viscosity coefficient, his treatment is far from conclusive. In support of this argument, the results of the Kinetic studies of Levitt based on direct simulation through molecular dynamics is presented where water molecules (considered as non-interacting hard spheres of 1A radius) are observed in a rigid cylindrical pores of 3.2A in radius and 11A long. The pore size, calculated following the procedures of pore flow models, is in good agreement with the physical size of the simulated pore. It is then concluded that the fundamental validity of the pore flow models in the case of tight membranes is yet unsettled, theoretically, but empirically its validity seems confirmed in some instances.

本文对孔隙流动模型进行了分类和简要评述,表明它们虽然有明显的差异,但却是等效的。事实证明,guout - elford - ferry的经典公式与Pappenheimer-Ussing和kedemm - katchalsky最近开发的公式之间的差异是由于在新公式中引入了更合适的膜内水的粘度系数。对模型中涉及的基本假设进行了重述,并提出了适用这些模型的标准。关于孔径公式的基本有效性的争论,当应用于紧膜时,连续流体力学变得可疑,进行了审查。Mikulecky最近对这种情况进行了理论分析,他简要介绍了计算孔径仅反映膜-水相互作用的程度。有人认为,由于他的分析忽略了膜-水相互作用对黏度系数的影响,他的处理远远没有结论性。为了支持这一观点,提出了基于分子动力学直接模拟的Levitt动力学研究的结果,其中水分子(被认为是半径为1A的非相互作用硬球体)在半径为3.2A,长为11A的刚性圆柱形孔隙中观察到。根据孔隙流动模型计算的孔隙尺寸与模拟孔隙的物理尺寸吻合较好。然后得出结论,在致密膜的情况下,孔隙流动模型的基本有效性在理论上尚未确定,但在某些情况下,它的经验有效性似乎得到了证实。
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引用次数: 0
Determination of the inner surface of macroporous ion exchange resins. 大孔离子交换树脂内表面的测定。
Pub Date : 1975-12-01
F Martinola, A Meyer

Study on macroporours IX resins and the pore structure. In addition to ion exchange reactions, macroporous ion exchange resins also show adsorptive properties which are due to the large pores of the resin beads and to the inner surface inside the beads. To measure this surface and the pore radii requires very precise fixation of the condition existing prior to the drying of the water-moist resin beads. Such stabilizing fixation can be achieved by displacing the regain water by isopropyl alcohol and subsequent drying for measuring the pore data.

大孔树脂及其孔隙结构的研究。除了离子交换反应,大孔离子交换树脂也表现出吸附性能,这是由于树脂珠的大孔和珠内表面。为了测量这个表面和孔半径,需要非常精确地固定在水湿树脂珠干燥之前存在的条件。这种稳定固定可以通过用异丙醇置换回水并随后干燥以测量孔隙数据来实现。
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引用次数: 0
On the properties of solid and liquid ion exchangers. II. Infrared and NMR studies of lithium and cesium salts of dinonylnaphtalene sulfonic acid in heptane. 固体和液体离子交换剂的性质。2庚烷中二烷基萘磺酸锂盐和铯盐的红外和核磁共振研究。
Pub Date : 1975-12-01
V Soldatov, L Odberg, E Högfeldt

Infrared and NMR measurements on solutions of lithium and cesium dinonylnaphtalene sulfonates (DNNS-salts) in heptane show that the state of water in these systems is in several respects similar to its state in solid ion exchange resins and in some respects also similar to that in ordinary water. The two cations differ in their interaction with the sulfonic acid group at low water contents, the interaction being stronger for Li+. Spin-lattice relaxation measurements on LiDNNS show that the state of lithium both in DNNS and in solid resins is quite different from that of lithium salts in aqueous solutions of the corresponding concentration.

对正庚烷中的锂和铯二烷基萘磺酸盐(dnns -盐)溶液的红外和核磁共振测量表明,这些体系中的水的状态在某些方面与固体离子交换树脂中的状态相似,在某些方面也与普通水中的状态相似。两种阳离子在低含水量时与磺酸基的相互作用不同,对Li+的相互作用更强。对LiDNNS的自旋晶格弛豫测量表明,锂在DNNS和固体树脂中的状态与锂盐在相应浓度水溶液中的状态有很大不同。
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引用次数: 0
A novel technique for the study of dry process membranes during their nascent phases. 研究干法膜初生阶段的新技术。
Pub Date : 1974-01-01
R E Kesting
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引用次数: 0
On the mechanism of ion exchange in crystalline zirconium phosphates. IX. The effect of crystallinity on Cs+ H+ exchange of alpha-zirconium phosphate. 结晶磷酸锆离子交换机理的研究。9结晶度对α -磷酸锆Cs+ H+交换的影响。
Pub Date : 1974-01-01
A Clearfield, A Oskarsson
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引用次数: 0
Chitosan membranes. 壳聚糖膜。
Pub Date : 1974-01-01
R A Muzzarelli, A Isolati, A Ferrero
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引用次数: 0
Transport phenomena in ion exchange membranes. Membrane potentials and solvent transference. 离子交换膜中的输运现象。膜电位和溶剂转移。
Pub Date : 1974-01-01
S D'Alessandro
{"title":"Transport phenomena in ion exchange membranes. Membrane potentials and solvent transference.","authors":"S D'Alessandro","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":77184,"journal":{"name":"Ion exchange and membranes","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1974-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15949589","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Noise measurements on ion transport across ion exchange membranes. 离子在离子交换膜上传输的噪声测量。
Pub Date : 1974-01-01
M E Green
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引用次数: 0
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Ion exchange and membranes
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