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Network rooms

Means of access to all system and network components (compnter rooms, network rooms/cabinets, cabling, etc.)... [Pg.857]

APC, Alternative Power Generation Technologies for Data Centres and Network Rooms , APC White Paper 64, 2003... [Pg.138]

Figure 10 Formation of linear and crosslinked polydimethylsiloxane networks. Room temperature vulcanization (RTV) is performed by reacting methoxysilyl-terminated polymer 75 and methyltrimethoxysilane 76. Hydrolysis produces transient silanols 77 and 78 whose dehydration yields silicone precursor 79. Two-part systems are based on the platinum-catalyzed addition reaction between vinyl-terminated polysiloxane 80 and polydimethylsiloxane carrying either only terminal 81 or multiple silane (Si-H) pendent groups. Silicone main chains of the resulting polymer 82 are linked through silicon-... Figure 10 Formation of linear and crosslinked polydimethylsiloxane networks. Room temperature vulcanization (RTV) is performed by reacting methoxysilyl-terminated polymer 75 and methyltrimethoxysilane 76. Hydrolysis produces transient silanols 77 and 78 whose dehydration yields silicone precursor 79. Two-part systems are based on the platinum-catalyzed addition reaction between vinyl-terminated polysiloxane 80 and polydimethylsiloxane carrying either only terminal 81 or multiple silane (Si-H) pendent groups. Silicone main chains of the resulting polymer 82 are linked through silicon-...
Concomitantly with the increase in hardware capabilities, better software techniques will have to be developed. It will pay us to continue to learn how nature tackles problems. Artificial neural networks are a far cry away from the capabilities of the human brain. There is a lot of room left from the information processing of the human brain in order to develop more powerful artificial neural networks. Nature has developed over millions of years efficient optimization methods for adapting to changes in the environment. The development of evolutionary and genetic algorithms will continue. [Pg.624]

The tertiary metal phosphates are of the general formula MPO where M is B, Al, Ga, Fe, Mn, etc. The metal—oxygen bonds of these materials have considerable covalent character. The anhydrous salts are continuous three-dimensional networks analogous to the various polymorphic forms of siHca. Of limited commercial interest are the alurninum, boron, and iron phosphates. Boron phosphate [13308-51 -5] BPO, is produced by heating the reaction product of boric acid and phosphoric acid or by a dding H BO to H PO at room temperature, foUowed by crystallization from a solution containing >48% P205- Boron phosphate has limited use as a catalyst support, in ceramics, and in refractories. [Pg.335]

The specific resistance of natural graphite crystals is ca Hem (room temperature) along the a axis parallel to the network basal plane. The resistance along the c axis (perpendicular to the basal plane) is ca 1 Q. The cja axis anisotropy ratio is, therefore, ca 10 . Screw dislocations within the crystal may short-circuit the current path parallel to the c axis and cause lower anisotropic ratios separation of planes may cause higher anisotropic ratios. [Pg.572]

Vulcanization. Generally this is carried out by the action of peroxides, which can cross-link the chains by abstracting hydrogen atoms from the methyl groups and allowing the resulting free radicals to couple into a cross-link. Some varieties of polysdoxanes contain some vinylmethyl siloxane units, which permit sulfur vulcanization at the double bonds. Some Hquid (short-chain) siHcones can form networks at room temperature by interaction between thek active end groups. [Pg.470]

Pure silica contains no metal ions and every oxygen becomes a bridge between two silicon atoms giving a three-dimensional network. The high-temperature form, shown in Fig. 16.3(c), is cubic the tetrahedra are stacked in the same way as the carbon atoms in the diamond-cubic structure. At room temperature the stable crystalline form of silica is more complicated but, as before, it is a three-dimensional network in which all the oxygens bridge silicons. [Pg.172]

In Chapters 3 and 11 reference was made to thermoplastic elastomers of the triblock type. The most well known consist of a block of butadiene units joined at each end to a block of styrene units. At room temperature the styrene blocks congregate into glassy domains which act effectively to link the butadiene segments into a rubbery network. Above the Tg of the polystyrene these domains disappear and the polymer begins to flow like a thermoplastic. Because of the relatively low Tg of the short polystyrene blocks such rubbers have very limited heat resistance. Whilst in principle it may be possible to use end-blocks with a higher Tg an alternative approach is to use a block copolymer in which one of the blocks is capable of crystallisation and with a well above room temperature. Using what may be considered to be an extension of the chemical technology of poly(ethylene terephthalate) this approach has led to the availability of thermoplastic polyester elastomers (Hytrel—Du Pont Amitel—Akzo). [Pg.737]

EXP AC analyzes an interconnected network of building rooms and ventilation systems. A lumped-parameter formulation is used that includes the effects of inertial and choking flow in rapid gas transienl.s. The latest version is specifically suited to calculation of the detailed effects of explosions in the far field using a parametric representation of the explosive event. A material transport capability models the effects of convection, depletion, entrainment, and filtration of... [Pg.362]

On cooling to room temperature after annealing, maraging steels transform completely to martensite. The as-annealed structure consists of packets of parallel lath-like martensite platelets arranged within a network of prior-austenite grain boundaries. The platelets have a high dislocation density but are not twinned. [Pg.563]

In terms of tonnage the bulk of plastics produced are thermoplastics, a group which includes polyethylene, polyvinyl chloride (p.v.c.), the nylons, polycarbonates and cellulose acetate. There is however a second class of materials, the thermosetting plastics. They are supplied by the manufacturer either as long-chain molecules, similar to a typical thermoplastic molecule or as rather small branched molecules. They are shaped and then subjected to either heat or chemical reaction, or both, in such a way that the molecules link one with another to form a cross-linked network (Fig. 18.6). As the molecules are now interconnected they can no longer slide extensively one past the other and the material has set, cured or cross linked. Plastics materials behaving in this way are spoken of as thermosetting plastics, a term which is now used to include those materials which can in fact cross link with suitable catalysts at room temperature. [Pg.916]

Wc have seen that molecular substances tend to have low melting points, while network, ionic, and metallic substances tend to have high melting points. Therefore, with a few exceptions, such as mercury, a substance that is liquid at room temperature is likely to he a molecular substance. Liquid solvents are heavily used in industry to extract substances from natural products and ro promote the synthesis of desired compounds. Because many of these solvents have high vapor pressures and so give off hazardous fumes, luinids that have low vapor pressures hut dissolve... [Pg.17]

Synthesis of comb (regular graft) copolymers having a PDMS backbone and polyethylene oxide) teeth was reported 344). These copolymers were obtained by the reaction of poly(hydrogen,methyl)siloxane and monohydroxy-terminated polyethylene oxide) in benzene or toluene solution using triethylamine as catalyst. All the polymers obtained were reported to be liquids at room temperature. The copolymers were then thermally crosslinked at 150 °C. Conductivities of the lithium salts of the copolymers and the networks were determined. [Pg.50]

Promoting the formation of supporf networks, wifh eifher physical or virfual meetings - members of a particular group (e.g. mentors or relationship supervisors) could have fheir own secure chat-room and notice board on the company intranet or on the Internet. To ensure that network meetings really take place, the scheme co-ordinator might want to make it his or her responsibility to schedule them and even, perhaps, facilitate them. [Pg.321]

This process is highly suitable for rubbers with poor solubility. In this process, the rubber sheet is soaked in TEOS or quite often in TEOS-solvent mixture and the in situ sUica generation is conducted by either acid or base catalysis. The sol-gel reaction is normally carried out at room temperature. Kohjiya et al. [29-31] have reported various nonpolar mbber-silica hybrid nanocomposites based on this technique. The network density of the rubber influences the swelling behavior and hence controls the silica formation. It is very likely that there has been a graded silica concentration from surface to the bulk due to limited swelling of the rubber. This process has been predominantly used to prepare ionomer-inorganic hybrids by Siuzdak et al. [48-50]. [Pg.62]

Figure 18.17 shows that the characteristics of the stress-strain curve depend mainly on the value of n the smaller the n value, the more rapid the upturn. Anyway, this non-Gaussian treatment indicates that if the rubber has the idealized molecular network strucmre in the system, the stress-strain relation will show the inverse S shape. However, the real mbber vulcanizate (SBR) that does not crystallize under extension at room temperature and other mbbers (NR, IR, and BR at high temperature) do not show the stress upturn at all, and as a result, their tensile strength and strain at break are all 2-3 MPa and 400%-500%. It means that the stress-strain relation of the real (noncrystallizing) rubber vulcanizate obeys the Gaussian rather than the non-Gaussian theory. [Pg.532]

Stimulated by these observations, Odelius et al. [73] performed molecular dynamic (MD) simulations of water adsorption at the surface of muscovite mica. They found that at monolayer coverage, water forms a fully connected two-dimensional hydrogen-bonded network in epitaxy with the mica lattice, which is stable at room temperature. A model of the calculated structure is shown in Figure 26. The icelike monolayer (actually a warped molecular bilayer) corresponds to what we have called phase-I. The model is in line with the observed hexagonal shape of the boundaries between phase-I and phase-II. Another result of the MD simulations is that no free OH bonds stick out of the surface and that on average the dipole moment of the water molecules points downward toward the surface, giving a ferroelectric character to the water bilayer. [Pg.274]


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See also in sourсe #XX -- [ Pg.65 ]




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