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Polyurethane matrix

The next approach to incorporate the 12F-diol into a polyurethane matrix was reaction of the y -12F-diol with aUphatic diacid chlorides (where a = 3 or 4) to give low molar mass polyesters (141) ... [Pg.540]

Composite Particles, Inc. reported the use of surface-modified rubber particles in formulations of thermoset systems, such as polyurethanes, polysulfides, and epoxies [95], The surface of the mbber was oxidized by a proprietary gas atmosphere, which leads to the formation of polar functional groups like —COOH and —OH, which in turn enhanced the dispersibility and bonding characteristics of mbber particles to other polar polymers. A composite containing 15% treated mbber particles per 85% polyurethane has physical properties similar to those of the pure polyurethane. Inclusion of surface-modified waste mbber in polyurethane matrix increases the coefficient of friction. This finds application in polyurethane tires and shoe soles. The treated mbber particles enhance the flexibility and impact resistance of polyester-based constmction materials [95]. Inclusion of treated waste mbber along with carboxyl terminated nitrile mbber (CTBN) in epoxy formulations increases the fracture toughness of the epoxy resins [96]. [Pg.1055]

Interfacial behavior of different silicones was extensively studied, as indicated in Section 3.12.4.6. To add a few more examples, solution behavior of water-soluble polysiloxanes carrying different pendant hydrophilic groups, thus differing in hydrophobicity, was reported.584 A study of the aggregation phenomena of POSS in the presence of amphiphilic PDMS at the air/water interface was conducted in an attempt to elucidate nanofiller-aggregation mechanisms.585 An interesting phenomenon of the spontaneous formation of stable microtopographical surface domains, composed primarily of PDMS surrounded by polyurethane matrix, was observed in the synthesis of a cross-linked PDMS-polyurethane films.586... [Pg.682]

Ciobanu, G., Carja, G., and Ciobanu, O. (2008) Structure of mixed matrix membranes made with SAPO-5 zeolite in polyurethane matrix. Micropor. Mesopor. Mater., 115 (1-2), 61-66. [Pg.351]

An interesting aspect of these experiments was the entrapment of activated charcoal in the hydrophilic polyurethane matrix. Givens and Sacks showed the potential of carbon-infused polyurethane foam as a filter medium. They showed a 99% removal efficiency of organics and nitrogenous compounds. While their study concerned domestic wastewater, the effect was assumed to be translatable to an aquaculture environment. [Pg.116]

In this regard, polyurethane technology offers a product designer a particular advantage. An aqueous solution or dispersion can be emulsified conveniently with a hydrophilic prepolymer and thus incorporated into the polyurethane matrix. The incorporation is accomplished by covalently bonding within the polyurethane backbone and by entrapping it within the matrix. Both methods are evident in foams produced by this technique. [Pg.141]

Delivery appheations are based on the fact that polyurethanes swell when exposed to solvents. Once a material is imbedded in a polyurethane matrix, the matrix can deliver the solvent or active ingredient in a number of ways including solubility and vapor pressure. Other polymer systems have this abihty, but the versatility of the polyurethane molecule (e.g., hydrophilicity or hydropobicity) gives it special properties. The abihty to produce polyurethanes as foams or elastomers grants product designers additional degrees of freedom. [Pg.173]

Our laboratory partnered with Josephine Bissing Dermaceuticals of Denver, CO, to develop delivery systems for certain skin care formulations that would eliminate the needs for surfactants, stabilizers, and emulsifiers. In effect, the hydrophilic polyurethane matrix in which the skin care formulation resides would replace all the stabilizing chemicals typically used in such formulations. [Pg.173]

The term elastomer is normally used to describe a material that will stretch when placed under load and will retract to approximately the original shape when the load is removed. The solid polyurethanes described so far have this elastic property. The elasticity differs from that of ordinary rubbers due to the nature of the bonds in the polyurethane matrix. [Pg.121]

ROS into more vital regions of the bacterial cells (note that S. aureus has no outer cell membrane). In recent research, it was demonstrated by Wilson that the photosensitizer methylene blue is more active on gold particles and kills even MRSA (with 2 log reductions after 10 min irradiation with green light) without degrading a polysiloxane or a polyurethane matrix and with only 10% photobleaching after 6 months [128]. [Pg.207]

Fig.20. The long-term stability (measured by TACAN Corporation) of a (PU-DR19) material. This material consists of a Disperse Red chromophore with one end attached to a polyurethane matrix. This long-term stability test was started in 1995 and no change in device halfwave voltage has been observed to the present time... Fig.20. The long-term stability (measured by TACAN Corporation) of a (PU-DR19) material. This material consists of a Disperse Red chromophore with one end attached to a polyurethane matrix. This long-term stability test was started in 1995 and no change in device halfwave voltage has been observed to the present time...
Fabrication methods have overwhelmingly focused on improving nanotube dispersion because better nanotube dispersion in polyurethane matrix has been found to improve the properties of the nanocomposites. The dispersion extent of CNTs in the polyurethane matrix plays an important role in the properties of the polymer nanocomposites. Similar to the case of nanotube/solvent suspensions, pristine nanotubes have not yet been shown to be soluble in polymers, illustrating the extreme difficulty of overcoming the inherent thermodynamic drive of nanotubes to bundle. Therefore, CNTs need to be surface modified before the composite fabrication process to improve the load transfer from the polyurethane matrix to the nanotubes. Usually, the polyurethane/CNT nanocomposites can be fabricated by using four techniques melt-mixing (15), solution casting (16-18), in-situ polymerization (19-21), and sol gel process (22). [Pg.144]

It should be pointed out that this method relies on the efficient dispersion of nanotubes in the relevant solvent. The choice of solvent is generally made based on the solubility of the polymer. However, pristine nanotubes usually cannot be well dispersed in most solvents. To get around this problem, Xia et al. (17) compared the dispersion of MWNT-graft-PU, MWNT-OH and raw MWNTs in 0.2% aqueous solution of sodium lauryl sulfate. The results showed that MWNT-graft-PU has a better dispersion stability compared to MWNTs and MWNT-OH. The incorporation of polyurethane-grafted carbon nanotubes had a better reinforcing effect compared to the raw carbon nanotubes. This should be attributed to the improved interfacial interaction between polyurethane matrix and carbon nanotubes. [Pg.146]

StelP has recently reported the results of an investigation of aluminum CMP on a variety of pads. An undisclosed company proprietary slurry and process was used to screen three pads — Rippey s MP-101 (a polyester fiber/polyurethane matrix), XP-601 (a grown-in-place, porometric polyurethane), and Rodel s IC-1000 (blown, microporous polyurethane). The results indicate high polish... [Pg.279]

Table 26. Spirwxazinc Bleaching Kinetics on a Polyurethane Matrix Measured after 30 minutes of Xenon Continuous Irradiation ( uv — cm 2 , — 14 klux r— 25 1 ) or during Hash-Photolysis Excitation ( , = 130J 50jlsl 7"= 331 C f... Table 26. Spirwxazinc Bleaching Kinetics on a Polyurethane Matrix Measured after 30 minutes of Xenon Continuous Irradiation ( uv — cm 2 , — 14 klux r— 25 1 ) or during Hash-Photolysis Excitation ( , = 130J 50jlsl 7"= 331 C f...
In another similar example nanocomposite was formed in a polyurethane matrix. Solvent soluble polyurethane had pyridine groups attached which formed complexes with metal salts. Films were then formed and subjected to a reducing agent in order to produce particulate metal filler. In this case the distribution of the filler which was formed was not uniform because the filler had tendency to aggregate (even though it was chemically attached to the matrix prior to the reduction). The following were factors controlling size and shape of these metal particles ... [Pg.348]

A polyurethane (x)/poly(methyl methacrylate) (1) system in which the methyl methacrylate was polymerized at various intervals after the gelation of the polyurethane was studied by Allen and coworkers (4). They found that for polymerizations at 50°C, increasing the postgelation time prior to acrylic formation decreased the size of the spherical poly(methyl methacrylate) particles that formed in the polyurethane matrix but had little effect on the shear moduli. [Pg.246]

An improved technique for entrapment of plant cells has been recently developed with Capsiaum frutesaene cell suspensions. Cells were shown to passively invade the pores of a reticulated polyurethane matrix, inside which viability and metabolic activity were better preserved than in other immobilizing matrices (23). This sytem was used in a deteuled study of the synthesis of capsaicin (an ester of vanillylamine), which is the pungent principle of chili pepper fruits. In the absence of specific precursors to capsaicin, the entrapped cells produced 2-3 orders of magnitude higher yields than c ll suspensions over a 5-10 day culture period (4-5 mg capsaicin g dry weight 1 versus 30 yg... [Pg.71]


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See also in sourсe #XX -- [ Pg.149 ]

See also in sourсe #XX -- [ Pg.65 , Pg.69 , Pg.73 , Pg.79 , Pg.84 ]




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