Interface-mediated formation of basic cobalt carbonate / polyethyleneimine composite microscrolls by strain-induced self-rolling

2021 ◽  
Author(s):  
Viktoria Gruen ◽  
Nicolas Helfricht ◽  
Sabine Rosenfeldt ◽  
Anna S Schenk

Polyethyleneimine aids the gas diffusion precipitation of nano-structured basic cobalt carbonate sheets at the air/solution interface. Upon drying, these mineral films undergo self-rolling into 3D coiled structures. Exploring this principle...

Author(s):  
Brigid R. Heywood ◽  
S. Champ

Recent work on the crystallisation of inorganic crystals under compressed monomolecular surfactant films has shown that two dimensional templates can be used to promote the oriented nucleation of solids. When a suitable long alkyl chain surfactant is cast on the crystallisation media a monodispersied population of crystals forms exclusively at the monolayer/solution interface. Each crystal is aligned with a specific crystallographic axis perpendicular to the plane of the monolayer suggesting that nucleation is facilitated by recognition events between the nascent inorganic solid and the organic template.For example, monolayers of the long alkyl chain surfactant, stearic acid will promote the oriented nucleation of the calcium carbonate polymorph, calcite, on the (100) face, whereas compressed monolayers of n-eicosyl sulphate will induce calcite nucleation on the (001) face, (Figure 1 & 2). An extensive program of research has confirmed the general principle that molecular recognition events at the interface (including electrostatic interactions, geometric homology, stereochemical complementarity) can be used to promote the crystal engineering process.


The Analyst ◽  
2020 ◽  
Vol 145 (1) ◽  
pp. 122-131 ◽  
Author(s):  
Wanda V. Fernandez ◽  
Rocío T. Tosello ◽  
José L. Fernández

Gas diffusion electrodes based on nanoporous alumina membranes electrocatalyze hydrogen oxidation at high diffusion-limiting current densities with fast response times.


1999 ◽  
Vol 2 (3) ◽  
pp. 263-275 ◽  
Author(s):  
Vladimir Koulich ◽  
Jose L. Lage ◽  
Connie C. W. Hsia ◽  
Robert L. Johnson, Jr.

Tellus B ◽  
2010 ◽  
Vol 62 (1) ◽  
Author(s):  
Natchaya Pingintha ◽  
Monique Y. Leclerc ◽  
John P. Beasley ◽  
Gengsheng Zhang ◽  
Chuckree Senthong

1982 ◽  
Vol 14 (4-5) ◽  
pp. 257-272 ◽  
Author(s):  
G Belfort ◽  
A Paluszek ◽  
L S Sturman

The Automated Hollow Fiber Ultrafiltration (AHFU) method is proposed here as a simple, efficient and rapid virus concentration technique from tap and drinking water sources. The results reported here extend the testing of the AHFU method to include two Picornaviruses [Poliovirus 2 (vaccine) and Echovirus 1] and Reovirus 3. Their respective mean virus recoveries from between 3 and 100 l of tap water is 88 ± 26, 79 ± 60, and 104 ± 48%. Various approaches including membrane surface modification, changes in backwash hydrodynamics, modification of the feed and backwash composition, and the use of S35-methionine labelled Poliovirus 2, are used to study the recovery of sorbed Poliovirus 2 from the hollow fiber/solution interface. An increase in the backwash pH to between 9.5 and 10.5 significantly improved Poliovirus 2 recovery. This, together with the labelled experiments, indicates that the virus-membrane interactions are probably electrostatic in nature. Convective polarization during filtration probably brings the virus close enough to the surface for these interactions to occur since virus losses were not detected for a non-permeation recycle experiment. Because very low Reynold's numbers are used, the flow is in the creeping-flow-regime for both filtration and backwashing (axial and radial). Unless significantly higher Reynolds could be used, enhanced recovery due to purely hydrodynamic forces is unlikely. High Reynold's numbers, of course, are limited by the pressure constraints of the hollow fibers.


1988 ◽  
Vol 53 (6) ◽  
pp. 1217-1228
Author(s):  
Petr Uchytil ◽  
Petr Schneider

Transport characteristics of four porous samples with bidisperse or broad monodisperse pore structure were determined by combination of diffusion and permeation measurements with simple gases and compared with results obtained from diffusion of toluene or α,α,α-trifluorotoluene in cyclohexane in liquid phase. From comparison of both types of results it followed that all pores are decisive for the rate of diffusional transport in liquids, whereas only the wide transport pores are significant in gas diffusion.


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