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Direct forming

When bringing a new material to the market, ease of forming with low tooling costs is advantageous, since a large variety of small series parts are likely to be produced. Low volume applications based on cheap tooling can be more suitable for early applications because they are often more labour intensive, whilst high volume applications are usually more sensitive to material costs and risks. These initial low volume applications can be used to show the potential of a new material. [Pg.63]

As shown in Fig. 17, the simplest route to produce composite laminates is by direct forming. Direct forming implies the creation of formed composites directly from fibre or tape of woven fabric without the addition of an intermediate consolidated laminate production step and subsequent thermoforming of the [Pg.63]

Since most self-reinforced polymer composite laminates described in literature are consolidated by thermal means, it is apparent that direct forming of composites in a final shape should also be feasible, if the shape is essentially a curved two-dimensimial structure without significant negative curvatures. The use of fabric reinforcement in different weave styles may dictate the complexity of the form, since difference weave styles are known to possess different drapabilities [235]. The use of male and female close-matched moulds should mean that processing of self-reinforced polymer composites based on technologies such as powder [Pg.64]

The use of a single-sided mould with a vacuum bagging process to apply pressure is a traditional low-investment composite process that can be used for both thermoplastic and thermoset matrix composites [236-240]. It was reported by Alcock et al. that it is possible to use a vacuum bag to apply atmospheric pressure ( 0.1 MPa) to achieve consolidation of coextruded PP tape composites directly from woven tape fabrics, to produce two-dimensional laminate structures [6] and also for more complicated geometries [23]. [Pg.65]


Before considering other concepts and group-theoretical machinery, it should once again be stressed that these same tools can be used in symmetry analysis of the translational, vibrational and rotational motions of a molecule. The twelve motions of NH3 (three translations, three rotations, six vibrations) can be described in terms of combinations of displacements of each of the four atoms in each of three (x,y,z) directions. Hence, unit vectors placed on each atom directed in the x, y, and z directions form a basis for action by the operations S of the point group. In the case of NH3, the characters of the resultant 12x12 representation matrices form a reducible representation... [Pg.594]

The mathematical model chosen for this analysis is that of a cylinder rotating about its axis (Fig. 2). Suitable end caps are assumed. The Hquid phase is introduced continuously at one end so that its angular velocity is identical everywhere with that of the cylinder. The dow is assumed to be uniform in the axial direction, forming a layer bound outwardly by the cylinder and inwardly by a free air—Hquid surface. Initially the continuous Hquid phase contains uniformly distributed spherical particles of a given size. The concentration of these particles is sufftcientiy low that thein interaction during sedimentation is neglected. [Pg.397]

Even when interaction is direct, forms of attack may be difficult to differentiate from other corrosion mechanisms. For example, corrosion beneath biological material can exhibit strikingly unique or vague attack morphologies according to the degree of microbiological involvement (see Chap. 6). [Pg.85]

Fig. 1.61 Erosion-corrosion. Impeller fabricated from Cu-10Sn-2Zn alloy used for pumping a slurry containing 5-10% H2SO4 after six months service. The blades of the impeller were extensively corroded. Note the directional form of the attack... Fig. 1.61 Erosion-corrosion. Impeller fabricated from Cu-10Sn-2Zn alloy used for pumping a slurry containing 5-10% H2SO4 after six months service. The blades of the impeller were extensively corroded. Note the directional form of the attack...
There are two main differences between the structure of the NH4NbOF4 chains and that of the Rb5Nb30Fi8 chains. The first difference is, that in the case ofRbjNbjOFu neighboring octahedrons along the chain are rotated by 7t/4 relative to one another (the rotation axis coincides with z-axis), as shown in Fig. 31. The second difference is that in the NbOF4 complexes, the niobium atoms are all shifted in the same direction, forming a polar structure. [Pg.87]

In rarer cases the ODNs also prevent normal gene transcription by directly forming triplex-helix structures with target DNA. This does not destroy a gene but prevents its unwinding or its binding to a gene promoter. [Pg.185]

Reaction of the carbanion of chloromethyl phenyl sulphoxide 409 with carbonyl compounds yields the corresponding 0-hydroxy adducts 410 in 68-79% yield. Each of these compounds appears to be a single isomer (equation 242). Treatment of adducts 410 with dilute potassium hydroxide in methanol at room temperature gives the epoxy sulphoxides 411 (equation 243). The ease of this intramolecular displacement of chloride ion contrasts with a great difficulty in displacing chloride ion from chloromethyl phenyl sulphoxide by external nucleophiles . When chloromethyl methyl sulphoxide 412 is reacted with unsymmetrical ketones in the presence of potassium tcrt-butoxide in tert-butanol oxiranes are directly formed as a mixture of diastereoisomers (equation 244). a-Sulphinyl epoxides 413 rearrange to a-sulphinyl aldehydes 414 or ketones, which can be transformed by elimination of sulphenic acid into a, 8-unsaturated aldehydes or ketones (equation 245). The lithium salts (410a) of a-chloro-/ -hydroxyalkyl... [Pg.327]

A similar question may also be asked for the indirect pathway Is COad directly formed by methanol decomposition, or does it result from a follow-up reaction. [Pg.444]

This approach of using the sulfide as the cathode implies that while nickel metal is directly formed on the cathode, the sulfur is continuously removed as hydrogen sulfide gas. In the former case there is a build up of sulfur in the cell. [Pg.723]

The inference is that the hydrofuranol ring of XL can never be directly formed by the saponification of a 3-tosyl ester of D-glucose, but only indirectly by the intermediate formation and scission of an anhydro ring of the ethylene oxide type. The sequence of reactions involved in the conversion of methyl 3-tosyl-jS-D-gIueoside into methyl 3,6-anhydro-n-glucoside is shown by XXXVI to XL. [Pg.69]

EC-ALE is the combination of UPD and ALE. Atomic layers of a compound s component elements are deposited at underpotentials in a cycle, to directly form a compound. It is generally a more complex procedure than most of the compound electrodeposition methods described in section 2.4.2, requiring a cycle to form each monolayer of the compound. However, it is layer-by-layer growth, avoiding 3-D nucleation, and offering increased degrees of freedom, atomic level control, and promoting of epitaxy. [Pg.8]

If the emitting species is not a reaction-product molecule directly formed by the exergonic reaction (as is the case in the luminol reaction, for example), chemiluminescence can occur via energy transfer processes ... [Pg.68]

CL reactions are commonly divided into two classes. In the type I (direct) reaction the oxidant and reductant interact with rate constant kr to directly form the excited product whose excited singlet state decays with the first (or pseudofirst)-order rate constant ks = kf+ kd. In the type II (indirect) reaction the oxidant and reactant interact with the formation of an initially excited product (kr) followed by the formation of an excited secondary product, either by subsequent chemical reaction or by energy transfer, with rate constant kA. The secondary product then decays from the lowest excited singlet state with rate constant kt. Type II reactions are generally denoted as complex or sensitized chemiluminescence. [Pg.76]

There are two common classes of CL reactions. In the type I reactions the oxidant and reductant interact to directly form the excited product whose excited... [Pg.80]

As the new atomic science, through ever more sophisticated detectors, opened a realm that could not be directly perceived by the physical senses, occult chemistry offered an alternative, a mode of scientific experimentation that could attempt to claim legitimacy through its scientific writing, charts, and visual illustrations of data while it also connected the human psyche to the subatomic world through a direct form of perception—that is, clairvoyance. (Theosophists argued that clairvoyance was indeed a sense faculty.) The conception of alchemy that supported such a vision was the spiritual alchemy we... [Pg.68]

Azolotriazines can be formed by cycloaddition reactions between diazoazoles and various substituted alkynes. In order to determine the mechanism of these reactions, semi-empirical AMI, MNDO, and PM3 calculations were run <1999JMT103>. Depending on the nature of the alkyne partner, these condensations may be viewed either as [7+2] cycloadditions, directly forming azolotriazines, or as [3+2] cycloadditions forming spirobicyclic intermediates, which quickly rearrange to azolotriazines. [Pg.631]

Direct food additives, 12 29, 34 categories of, 22 30 function of, 22 30 Direct formed polyimides, 20 284 Direct fuel cells, 22 221 Direct-gap semiconductors, 14 837 ... [Pg.278]

The simplest of structures is the rock salt structure, depicted in Figure 2.2a. Magnesium oxide is considered to be the simplest oxide for a number of reasons. It is an ionic oxide with a 6 6 octahedral coordination and it has a very simple structure — the cubic NaCl structure. The structure is generally described as a cubic close packing (ABC-type packing) of oxygen atoms in the (111) direction forming octahedral cavities. This structure is exhibited by other alkaline earth metal oxides such as BaO, CaO, and monoxides of 3d transition metals as well as lanthanides and actinides such as TiO, NiO, EuO, and NpO. [Pg.43]


See other pages where Direct forming is mentioned: [Pg.209]    [Pg.124]    [Pg.320]    [Pg.402]    [Pg.40]    [Pg.437]    [Pg.16]    [Pg.788]    [Pg.508]    [Pg.475]    [Pg.563]    [Pg.573]    [Pg.327]    [Pg.27]    [Pg.82]    [Pg.729]    [Pg.14]    [Pg.213]    [Pg.25]    [Pg.216]    [Pg.333]    [Pg.192]    [Pg.68]    [Pg.385]    [Pg.195]    [Pg.170]    [Pg.144]    [Pg.177]    [Pg.194]    [Pg.106]    [Pg.102]    [Pg.327]    [Pg.732]   
See also in sourсe #XX -- [ Pg.235 ]




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