Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Coordination polymer particles

A similar strategy was followed by Xin et al. to produce Zn(ICA) (ZIF-90, where ICA=iinidazole-2-carboxyaldehyde) with triethylamine (TEA) as the deprotonating agent at room temperatime. TEA was also employed to manipulate the particle size and shape of [Cu3(btc)2] and a coordination polymer particle by mixing 4,40-dicarboxy-2,20-bipyridine (H2dcbp) and Cu(OAc)2 in mixed solvents of water at room temperatme. ... [Pg.5]

Polymer Particle Balances (PEEK In the case of multiconponent emulsion polymerization, a multivariate distribution of pjarticle propierties in terms of multiple internal coordinates is required in this work, the polymer volume in the piarticle, v (continuous coordinate), and the number of active chains of any type, ni,n2,. .,r n (discrete coordinates), are considered. Therefore... [Pg.381]

Figure 8. Examples of electrostatic immobilization of POMs (a) on the surface of (Si/A102)" particles [107] and (b) within nanocage of on MIL-101 coordination polymer [126]. Figure 8. Examples of electrostatic immobilization of POMs (a) on the surface of (Si/A102)" particles [107] and (b) within nanocage of on MIL-101 coordination polymer [126].
Oh M, Mirkin CA. Chemically tailorable colloidal particles fi-om infinite coordination polymers. Nature 2005 438 651-654. [Pg.177]

Fig. 31. Computed conversion of the polymer particle as a function of the axial coordinate for cases with and without accounting for existing velocity and temperature gradients in the LEFR. Fig. 31. Computed conversion of the polymer particle as a function of the axial coordinate for cases with and without accounting for existing velocity and temperature gradients in the LEFR.
Fig. 6.2. Synthetic strategy for the preparation of surface imprinted metal-coordinating polymers using poly(TRIM) particles. Fig. 6.2. Synthetic strategy for the preparation of surface imprinted metal-coordinating polymers using poly(TRIM) particles.
Modified poly(methacrylic acid) microparticles complexed with gadolinium(lll) (Gd ) ions were prepared at 100 nm by Michinobu [81]. The emulsion tcrpolymerization of methacryhc acid, ethyl acrylate, and aUyl methacrylate and the following complexation with Gd ions yielded the polymer particles with different Gd ion contents. Potentiometric titration of the complexation of the particle with Gd + ions indicated the formation of a very stable tris-carboxylate coordinate complex with the Gd + ion. The microparticles dispersed on a mica substrate were subjected to AFM, followed by MFM. AFM showed 100-nm-sized and monodispersed spherical images. The following MFM... [Pg.397]

For all of the samples studied and for particle sizes down to the lowest studied, 150 nm, very similarly shaped SCO transition curves were observed and taken to imply that no significant size effect influenced the SCO process, at least in these particular nano-objects. Nanocrystals of the 3D coordination polymer [Fe(prazine)Pt(CN)4], which displays SCO properties in the bulk, also preserve the same magnetic, structural and optical bistability for particle sizes on the order of 50 nm. Recent evidence suggests however that this may not always be the case, as in the example of the 2D coordination polymer [Fe(3-fluoropyridine)2M(CN)4] where the bulk SCO properties were shown to be very markedly influenced by the nanoparticle dimen-sions. Detailed discussion of this topic falls outside the scope of this review but we refer to it here because it is an aspect of spin crossover studies that bears fundamentally" " on the practical application in device teehnology of nano-dimensioned SCO materials, which continue to display hysteretie behaviour at such dimensions. [Pg.87]

Polymerization of ethylene is often carried out in gas-phase using a heterogeneous coordination catalyst [22]. Polymer is formed on the active sites of the catalyst forming an expanding catalyst-polymer particle. The gaseous monomer diffuses through the pores of the particle and through the polymer to reach the active sites. [Pg.18]

Manipulation of PSDs is generally attained through modification of surfactant concentrations (mostly in emulsion polymerizations) [48,49], agitation speeds (mostly in suspension polymerizations) [50], and initial catalyst size distributions and reaction times (residence time distributions in continuous reactors, mostly in coordination polymerizations) [51]. Effects of agitation speeds and surfactant concentrations on the PSD of polymer particles produced in suspension and emulsion polymerizations are discussed in detail in Chapters 5 and 6, respectively. When the catalyst is fed into the reactor as a solid material, as in typical polyolefin reactions, then the residence times and the initial PSD of the catalyst particles are used to manipulate the PSD of the final polymer product. Similar strategies are used in seeded emulsion polymerizations, where an initial load of preformed particles can be used to improve the control over the concentration of polymer particles in the latex and over the PSD of the final polymer product. [Pg.321]

Hydrogenation is the most well studied area among immobilized palladium catalysis. While a great majority of the applications focused on the use of support such as alumina and activated carbon, a great diversity of novel support systems have been reported in recent years, aimed at finding a catalyst with a well-characterized coordination sphere and tailor-made activity. Pd(0) catalysts dispersed on crosslinked styrene-divinylbenzene copolymers have been prepared by impregnation of lipophilic complexes followed by reduction with hydrazine. It was found that the functional groups in the polymer as well as polymer particle sizes had a major effect on catalyst activity.t [i53]-[i95]... [Pg.1348]

Classical trajectory calculations are used to develop an understanding of the experimentally observed behavior of collisions and surface interactions of nano-and micro-scale polymer particles on Si, C, and Al surfaces in a vacuiun. The PE particles were propagated up to 100 ps for those surfaces to investigate the selforganization of polymer particles (mechanical memory) via coUisions. At the start of classical trajectory, the initial values of the Cartesian momenta, p, were given randomly in the amorphous particle to set the initial temperature to 300 K, and the system was subjected to zero center-of-mass position and velocity. After the surface was set at 10 C from the closest atom of the particle in z coordinate, a desired initial translational velocity, was assigned to all atoms of the particle in z direction... [Pg.59]

The polymerization of olefins with coordination catalysts is performed in a large variety of polymerization processes and reactor configurations that can be classified broadly into solution, gas-phase, or slurry processes. In solution processes, both the catalyst and the polymer are soluble in the reaction medium. These processes are used to produce most of the commercial EPDM rubbers and some polyethylene resins. Solution processes are performed in autoclave, tubular, and loop reactors. In slurry and gas-phase processes, the polymer is formed around heterogeneous catalyst particles in the way described by the multigrain model. Slurry processes can be subdivided into slurry-diluent and slurry-bulk. In slurry-diluent processes, an inert diluent is used to suspend the polymer particles while gaseous (ethylene and propylene) and liquid (higher a-olefins) monomers are fed into the reactor. On the other hand, only liquid monomer is used in the slurry-bulk pro-... [Pg.416]

Daiguetxnme C, Kerbellec N, Guillou O et al (2008) Structural and luminescent properties of micro- and nanosized particles of lanthanide terephthalate coordination polymers. Inorg Chem 47 3700-3708... [Pg.84]


See other pages where Coordination polymer particles is mentioned: [Pg.43]    [Pg.43]    [Pg.126]    [Pg.78]    [Pg.160]    [Pg.242]    [Pg.29]    [Pg.159]    [Pg.313]    [Pg.313]    [Pg.159]    [Pg.113]    [Pg.915]    [Pg.68]    [Pg.99]    [Pg.469]    [Pg.2]    [Pg.445]    [Pg.309]    [Pg.469]    [Pg.1203]    [Pg.159]    [Pg.92]    [Pg.58]    [Pg.395]    [Pg.395]    [Pg.102]    [Pg.106]    [Pg.110]    [Pg.334]    [Pg.203]    [Pg.705]    [Pg.640]    [Pg.64]   
See also in sourсe #XX -- [ Pg.43 ]




SEARCH



Coordinating polymers

Polymer coordination

Polymer particles

Polymers coordinated

© 2024 chempedia.info