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Molecular with ultrahigh

Single-walled carbon nanotubes (SWNTs) had been considered for the crossbar components of the defect-tolerant molecular computers but they have been found to be too difficult to handle due to their insolubility and their tendency to form bundles or ropes. Instead, metallic nanowires have become the materials of choice used in the construction of the crossbar devices, with ultrahigh-density lattices and circuits being built, having groups of nanowires 8 nm in diameter and 16 nm apart in layers perpendicular to each other to create nanowire junction densities of 1011 per cm2.52 The process does not depend on self-assembly but rather on molecular beam epitaxy. [Pg.87]

In order to verify the existence of this barrier to dissociation, we have used molecular beam techniques coupled with ultrahigh vacuum surface electron spectroscopies to monitor the extent of dissociation as a function of the transla-... [Pg.52]

Warner, J. H., Ito, Y., Riimmeli, M. H., Buchner, B., Shinohara, H., and Briggs, G. A. D. 2009. Capturing the motion of molecular nanomaterials encapsulated within carbon nanotubes with ultrahigh tempoi al resolution. ACS Nano 3 3037-3044. [Pg.489]

The wear resistance of zirconia is inferior to that of alumina. In ceramic/ceramic combinations the wear rate of zirconia can be significantly higher than that of alumina. In combination with ultrahigh-molecular-weight polyethylene (UHMWPE) excessive wear of the polymer occurs. [Pg.640]

DMS described above [10]. It is important to note that the structural isomers of xylene (meta-, para-, and ortho-) have the same molecular weight, but they differ in position of the second methyl group. Ortho-xylene is 1,2-dimethylbenzene meta-xylene is 1,3-dimethylbenzene and para-xylene is 1,4-dimethylbenzene. At low electric field, they have similar cross section and can only be separated by an ion mobility spectrometer with ultrahigh resolving power. However, owing... [Pg.2259]

Kuznetsov et al. (2001) used composite membranes, coated with poly(2-dimethyl-amino ethyl)methacrylate (PDMA) and ladder polyorganosiloxane (LP) onto micro-porous aromatic PAI support and PAN, as PV membranes for separating mixtures of methanol and MTBE. It was noticed that the PAI and PAN supports of the multilayer m branes have opposite effects on the total selectivity. High membrane permeability of the multilayer membranes was attained by virtue of the thinness of the interlayer or coating diffusion layer of PDMA with ultrahigh molecular weight. [Pg.284]

Warner JH, Ito Y, Riimmeli MH, Buchner B, Shinohara H, Briggs GAD. Capturing the motion of molecular nanomalerials encapsulated within carbon nanotubes with ultrahigh temporal resolution. ACS Nano 2009 3 3037-44. [Pg.154]

Inverse emulsion polymerization is used for the preparation of polymers with ultrahigh molecular masses. For this type of polymerization, the expression dispersion polymerization is often used in the literature [410]. A concentrated monomer solution (about 40% monomer in water) is dispersed under intensive stirring in aliphatic or aromatic hydrocarbons in the presence of additives (emulsifiers, protective colloids). Polymerization can be initiated by either water-soluble or oil-soluble initiators [411-418]. The advantage of this process is based on the constant viscosity of the reaction mixture, as the increase of viscosity takes place only in the dispersed phase. By the use of additives (tensides), the dispersion inverts when the emulsion is stirred into water. Precipitation from the aqueous solution yields a polymer with ultrahigh molar mass. The quality of polymer made by inverse emulsion polymerization is influenced by the following factors (1) species and concentration of initiator, (2) species and concentration of additives (emulsifiers, protective colloids), (3) type of oil phase, and (4) particle size of the dispersed water phase. Because of the easy modification of all these parameters, much attention has been given in recent years to water-in-oil emulsion polymerization of AAm and MAAm. [Pg.286]

When potassium titanate whiskers modified by a coupling agent are filled into PE material with ultrahigh molecular weight, the hardness of composite material increases significantly, as shown in Table 4.5. [Pg.187]

Zhao, Y. Y., Q. B. Yang, X. F. Lu, C. Wang, and Y. Wei (2005). Study on correlation of morphology of electrospun products of polyacrylamide with ultrahigh molecular weight. Journal of Polymer Science Part B Polymer Physics... [Pg.385]

Fig. 36. Electrical conductivity of PANI(DBSA)i q solution blended in decanol with ultrahigh-molecular-weight polyethylene. Adapted from Y. Cao, P. Smith, and A. J. Heeger, U.S. Patent 5,232,631,1993. Fig. 36. Electrical conductivity of PANI(DBSA)i q solution blended in decanol with ultrahigh-molecular-weight polyethylene. Adapted from Y. Cao, P. Smith, and A. J. Heeger, U.S. Patent 5,232,631,1993.
The solubility in common solvents allows preparation of polymer blends based on solvent casting. Figure 36 shows the conductivity of PANI(DBSA)i,o solution blended with ultrahigh-molecular-weight polyethylene (UHMWPE) at different concentrations after evaporation of the xylene solvent [187, 188]. A low percolation limit can thus be obtained in solution processing of commodity polymers. Corresponding results are also obtained in blends with other polymers, such as polystyrene and polyamide 12. [Pg.202]

There is another beautiful experiment which is even more convincing in its support of the reptation model. Fluorescence microscopy enables the motion of fluorescently stained single chains to be directly observed. The technique was applied to a concentrated solution of monodisperse DNA-molecules with ultrahigh molecular weight corresponding to a contour length in the 100 /xm-range. On one end of the chain, an especially coated 1 /xm-diameter... [Pg.286]


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See also in sourсe #XX -- [ Pg.17 ]




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