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Polymeric inert material

Hybrid rockets are intermediate between solid rockets and hquid rockets in terms of the nature of the combination of solid fuel and hquid oxidizer. Since the fuel and oxidizer components of a Hquid rocket are physically separated, two mechanical systems are needed to feed these components into the combustion chamber. On the other hand, a hybrid rocket uses a polymeric inert material as a fuel and a Hquid oxidizer, and so only one mechanical system is needed to feed this Hquid oxidizer into the combusHon chamber. [Pg.430]

There are six stabilization techniques currently available however, only two of them have found widespread application. These are cementation and stabilization through the addition of lime and fly ash.25 26 There is currently developmental work being undertaken to make use of bitumen, paraffin, and polymeric materials to reduce the degree to which metals can be taken into solution. Encapsulation with inert materials is also under development. [Pg.376]

A simple method of effectively preventing accumulation of dangerously high concentrations of peroxidic species in distillation residues is that detailed in an outstanding practical textbook of preparative acetylene chemistry [2], The material to be distilled is mixed with an equal volume of non-volatile mineral oil. This remains after distillation as an inert diluent for polymeric peroxidic materials. [Pg.328]

The following two approaches to rendering Compn B type expls more insensitive were investigated and reported in Ref 46 the first by coating the RDX crystals with inert materials such as waxes and/or polymeric compds of sufficiently high melting points to prevent their remelting in molten TNT or at ordinary steam temp, and the second by the addition of a wax directly to Compn B by means of a wax/TNT emulsion. [Pg.341]

The extraordinary versatility of this polymeric plastic material, which has made it one of the most widely used of the myriad of polymers and copolymers available today, is demonstrated by its range of end uses. PVC products have properties that combine strength, lightness, and inertness with a wide range of resilience, excellent color acceptance, electrical insulating properties, crystal-like clarity, and the ability to be processed easily by many methods into a tremendous variety of forms. [Pg.195]

The exact nature of the beginning and end of such a polymer chain is not certain. In general, the polymer can be characterized by its average degree of polymerization, i.e., the value of n, or more precisely by the distribution of n values. The heat of polymerization is 17.4 0.2 kcal/mole at 26.19°C. The reaction may be initiated by heat or by means of catalysts. Organic peroxides are typical initiators. Styrene also will polymerize in the presence of various inert materials, such as solvents, fillers, dyes, pigments, plasticizers, rubbers, and resins. Moreover, it forms a variety of copolymers with other mono- and polyvinyl monomers. [Pg.1354]

Polymerization is only rarely limited to the interaction of a monomer with the initiator, transfer agent or impurity. Each component of the system, including the so-called inert materials, participates in polymer formation. The mutual interaction of various components with the monomer may vary from a simple physical process to a complicated chemical reaction. In all cases intermolecular forces are involved, as manifested by the formation of solvates, associates and complexes. Sometimes it is difficult to determine the poorly defined boundary between physical and chemical processes. [Pg.61]

Some of these reactions use finely divided metals (often supported on an inexpensive inert material, often an oxide or a clay mineral) while others use metal compounds e.g., molybdenum sulfide for hydrodesulfurization (Section 3.2.3), tunsten oxide (for metathesis. Section 6.3), or titanium or chromium salts (for olefin polymerization. Section 7.3). [Pg.270]

While polymeric photorefractive materials can be prepared by adding separate molecules for photo-generation, charge transport and non-linear optical response into an inert polymer, most systems studied use polymers where one or more of these components are covalently bonded to the polymer. Polymer... [Pg.410]

The presence of insoluble materials in the polymerization mixture may have some control on the structure of the polymeric skeleton. Seidl et al. reported that the micro structure of skeletons of ion-exchange resins, based on the copolymers of styrene and DVB, can be controlled by carrying out the polymerization in presence of an inert material and by adjusting the reaction conditions and concentration of DVB. The micro structure depends on the parameter of interaction and on the molar volume of the inert material. In the case of copolymers modified by an inert component with high molar volume and interaction parameters, microstructures with small measureable surfaces and pores with relatively large radii are obtained. [Pg.94]

In the literature, thermally regenerable resins have also been referred to as composite resins. However, the thermally regenerable resins are dealt with in a separate section as the developments in this new field are quite significant. Mainly, the systematic approach on the manipulation of polymerization procedures to obtain resins having the maximum thermally regenerable capacity is discussed. The Section on composite resins deals with resin systems which incorporate inert materials and magnetic particles. [Pg.113]

Direct feedback of recovered monomer in recycle copolymerization may lead to buildup of inert materials that can affect the polymerization reaction. This point is illustrated in the copolymerization of styrene and a-methylstyrene. A 22-day experiment was conducted in which the feed was a mixture of 25% a-methylstyrene and 75% styrene and polymerization was effected at 125° C. The monomer contained about 0.5% of inerts, consisting primarily of ethylbenzene... [Pg.232]

Way, Noble and Bateman (49) review the historical development of immobilized liquid membranes and propose a number of structural and chemical guidelines for the selection of support materials. Structural factors to be considered include membrane geometry (to maximize surface area per unit volume), membrane thickness (<100 pm), porosity (>50 volume Z), mean pore size (<0.1)jm), pore size distribution (narrow) and tortuosity. The amount of liquid membrane phase available for transport In a membrane module Is proportional to membrane porosity, thickness and geometry. The length of the diffusion path, and therefore membrane productivity, is directly related to membrane thickness and tortuosity. The maximum operating pressure Is directly related to the minimum pore size and the ability of the liquid phase to wet the polymeric support material. Chemically the support must be Inert to all of the liquids which It encounters. Of course, final support selection also depends on the physical state of the mixture to be separated (liquid or gas), the chemical nature of the components to be separated (inert, ionic, polar, dispersive, etc.) as well as the operating conditions of the separation process (temperature and pressure). The discussions in this chapter by Way, Noble and Bateman should be applicable the development of immobilized or supported gas membranes (50). [Pg.13]

Man-made usage of binding enzymes onto solid materials goes back to the 1950s, when immobilized enzymes, that is enzymes with restricted mobility, were first prepared intentionally [1,2]. Immobilization was achieved by inclusion into polymeric matrices or binding onto carrier materials. Considerable effort was also put into the cross-linking of enzymes, either by cross-linking of protein alone or with the addition of inert materials [3]. [Pg.96]

Non-porous membranes can be used for extraction of polar and non-polar compounds from liquid samples using only minimal amount of organic solvent. A non-porous membrane is a liquid or a solid (e.g. polymeric) phase sandwiched between two other phases, usually aqueous but can also be gaseous (8). One of these two phases contains the components to be extracted, i.e. the donor phase. On the other side of the membrane is the acceptor phase, i.e. where the extracted components are collected. Usually, the membrane unit is made of two blocks of inert material with a machined groove in each. The membrane is placed in-between these blocks and clamped together, so that a channel (typically 10-1000... [Pg.13]

Metal oxides supported on finely divided inert materials have been useful for polymerization of ethylene and other vinyl monomers. The mechanism is presumably similar to that of heterogeneous Ziegler-Natta polymerization with initiation... [Pg.569]

Frontal polymerization in the presence of an inert material, Journal of Engi-... [Pg.241]

Because of the diversity of applications of modem liquid chromatography, there is no universal column packing material. StiU, a more or less ideal HPLC packing should be inert toward analytes, pH stable, and compatible with both nonpolar and polar organic solvents and even water, and allow fast diffusion of analytes in the interior of the sorbent bead. These conditions are best met by the new, third generation of polymeric adsorbent materials, hypercrosslinked polystyrenes. A rigid open-work-type hypercrosslinked network displays extremely high apparent specific surface area (up to... [Pg.507]


See other pages where Polymeric inert material is mentioned: [Pg.6]    [Pg.380]    [Pg.340]    [Pg.141]    [Pg.11]    [Pg.9]    [Pg.354]    [Pg.163]    [Pg.271]    [Pg.231]    [Pg.71]    [Pg.2023]    [Pg.63]    [Pg.21]    [Pg.497]    [Pg.82]    [Pg.1548]    [Pg.71]    [Pg.94]    [Pg.242]    [Pg.80]    [Pg.20]    [Pg.353]   
See also in sourсe #XX -- [ Pg.430 ]

See also in sourсe #XX -- [ Pg.430 ]




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