Pore structure organic polymer

The control of the pore size of porous silica gel by the structure of the organic polymer has been accomplished by using the so-called starburst dendrimer as an... 

Sol-gel processing forms the basis for various routes employed for the fabrication of a wide diversity of functional materials. To impart a structural organization at various length scales, the syntheses are performed using templates. Most consist of a self-organized ensemble of surfactants and co-polymers [1-10]. They have been successfully applied to control the geometry and dimensions of pores that are periodically arranged as in the initial structures. Mesoporous silica materials of the MCM family, which were first synthesized by a team from the Mobil oil company [11,12], are a well-known example. 

Small-pore zeolite Nu-6(2) has a NSI-type structure and two different types of eight-membered-ring channels with limiting dimensions of 2.4 and 3.2 A [54]. Gorgojo and coworkers developed mixed-matrix membranes using Nu-6(2) as the dispersed zeolite phase and polysulfone Udel as the continuous organic polymer phase [55]. These mixed-matrix membranes showed remarkably enhanced H2/ CH4 selectivity compared to the bare polysulfone membrane. The H2/CH4 selectivity increased from 13 for the bare polysulfone membrane to 398 for the Nu-6(2)/ polysulfone mixed-matrix membranes. This superior performance of the Nu-6(2)/ polysulfone mixed-matrix membranes is attributed to the molecular sieving role played by the selected Nu-6(2) zeoHte phase in the membranes. 

The differences of the intrusion and extrusion mechanisms are the main factors, leading to the different pathways (hysteresis) of the branches in Fig. 1.16A. Furthermore, this effect causes the pore size distribution obtained from the intrusion curve to be incorrectly shifted towards smaller pore sizes. Unlike some inorganic materials of very regular pore structure (e.g. zeolites), permanently porous organic polymers consist of a very complex network of pores of different sizes connected to each other. Correction of these falsifications in the results described above is virtually impossible, since it implies a detailed understanding of the network. 

The size-exclusion and ion-exchange properties of zeolites have been exploited to cause electroactive species to align at a zeolite—water interface (233—235). The zeolite thus acts as a template for the self-organization of electron transfer (ET) chains that may find function as biomimetic photosynthetic systems, current rectifiers, and photodiodes. An example is the three subunit ET chain comprising Fe(CN )g anion (which is charge-excluded from the anionic zeolite pore structure), Os( bipyridine (which is an interfacial cation due to size exclusion of the bipyridine ligand), and an intrazeolite cation (trimethylamino)methylferrocene+ (F+ ). A cationic polymer bound to the (CN)6 anion holds the self-assembled structure at an... 

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