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Metallic block metals

All calorimeters consist of the calorimeter proper and its surround. This surround, which may be a jacket or a batii, is used to control tlie temperature of the calorimeter and the rate of heat leak to the environment. For temperatures not too far removed from room temperature, the jacket or bath usually contains a stirred liquid at a controlled temperature. For measurements at extreme temperatures, the jacket usually consists of a metal block containing a heater to control the temperature. With non-isothemial calorimeters (calorimeters where the temperature either increases or decreases as the reaction proceeds), if the jacket is kept at a constant temperature there will be some heat leak to the jacket when the temperature of the calorimeter changes. [Pg.1901]

Clusters are intennediates bridging the properties of the atoms and the bulk. They can be viewed as novel molecules, but different from ordinary molecules, in that they can have various compositions and multiple shapes. Bare clusters are usually quite reactive and unstable against aggregation and have to be studied in vacuum or inert matrices. Interest in clusters comes from a wide range of fields. Clusters are used as models to investigate surface and bulk properties [2]. Since most catalysts are dispersed metal particles [3], isolated clusters provide ideal systems to understand catalytic mechanisms. The versatility of their shapes and compositions make clusters novel molecular systems to extend our concept of chemical bonding, stmcture and dynamics. Stable clusters or passivated clusters can be used as building blocks for new materials or new electronic devices [4] and this aspect has now led to a whole new direction of research into nanoparticles and quantum dots (see chapter C2.17). As the size of electronic devices approaches ever smaller dimensions [5], the new chemical and physical properties of clusters will be relevant to the future of the electronics industry. [Pg.2388]

A skilled worker can use a micro-Bunsen burner for most types of heating. Nevertheless, as there is a tendency for a liquid to shoot out of a small test tube when heated, it is preferable to place the tube in a hot water-bath or in a metal heating block. A small glycerol bath is suitable for distillations and heating under reflux, the glycerol being subsequently easily removed from flasks, etc., by washing with water. [Pg.60]

Sublimation. This is a most useful process for small-scale work as the losses are comparatively small. This can be performed (a) In a long narrow tube sealed at one end. The material is shaken to the closed end of the tube, which is then inserted horizontally in a metal-heating block (Fig. 50) (b) In the cold-finger device (Fig. 35, p. 62)-... [Pg.69]

BackTitrations. In the performance of aback titration, a known, but excess quantity of EDTA or other chelon is added, the pH is now properly adjusted, and the excess of the chelon is titrated with a suitable standard metal salt solution. Back titration procedures are especially useful when the metal ion to be determined cannot be kept in solution under the titration conditions or where the reaction of the metal ion with the chelon occurs too slowly to permit a direct titration, as in the titration of chromium(III) with EDTA. Back titration procedures sometimes permit a metal ion to be determined by the use of a metal indicator that is blocked by that ion in a direct titration. Eor example, nickel, cobalt, or aluminum form such stable complexes with Eriochrome Black T that the direct titration would fail. However, if an excess of EDTA is added before the indicator, no blocking occurs in the back titration with a magnesium or zinc salt solution. These metal ion titrants are chosen because they form EDTA complexes of relatively low stability, thereby avoiding the possible titration of EDTA bound by the sample metal ion. [Pg.1167]

After the block is chucked in the lathe, the lathe turns the block against the knife and peels the veneer in a continuous sheet as the knife moves toward the center of the block. When the knife cannot advance further without moving into the metal chucks, the lathe is stopped, the core of the block is dropped, the lathe is recharged, and the cycle repeated. [Pg.383]

A brief review has appeared covering the use of metal-free initiators in living anionic polymerizations of acrylates and a comparison with Du Font s group-transfer polymerization method (149). Tetrabutylammonium thiolates mn room temperature polymerizations to quantitative conversions yielding polymers of narrow molecular weight distributions in dipolar aprotic solvents. Block copolymers are accessible through sequential monomer additions (149—151) and interfacial polymerizations (152,153). [Pg.170]

The dark blue solution containing 5—10% of cellulose with a DP of 1000—2000 is filtered through a series of plate-and-frame filter presses using fine mesh metal screens to remove any particles that might block the spinneret holes. It is then deaerated under vacuum and stored ready for spinning. Unlike viscose dope, the cuprammonium cellulose [9050-09-3] solution is relatively stable. [Pg.351]

GopolymeriZation Initiators. The copolymerization of styrene and dienes in hydrocarbon solution with alkyUithium initiators produces a tapered block copolymer stmcture because of the large differences in monomer reactivity ratios for styrene (r < 0.1) and dienes (r > 10) (1,33,34). In order to obtain random copolymers of styrene and dienes, it is necessary to either add small amounts of a Lewis base such as tetrahydrofuran or an alkaU metal alkoxide (MtOR, where Mt = Na, K, Rb, or Cs). In contrast to Lewis bases which promote formation of undesirable vinyl microstmcture in diene polymerizations (57), the addition of small amounts of an alkaU metal alkoxide such as potassium amyloxide ([ROK]/[Li] = 0.08) is sufficient to promote random copolymerization of styrene and diene without producing significant increases in the amount of vinyl microstmcture (58,59). [Pg.239]

The first successhil use of lithium metal for the preparation of a i7j -l,4-polyisoprene was aimounced in 1955 (50) however, lithium metal catalysis was quickly phased out in favor of hydrocarbon soluble organ olithium compounds. These initiators provide a homogeneous system with predictable results. Organ olithium initiators are used commercially in the production of i7j -l,4-polyisoprene, isoprene block polymers, and several other polymers. [Pg.467]

Porous P/M products can be sinter bonded to soHd metals. They can also be welded, brazed, or soldered. Filling the voids with flux or molten metal has to be avoided. P/M porous products can be machined, but blocking of the porous passages has to be avoided. Press fitting and epoxy bonding are commonly used. [Pg.189]

Friction Materials. Sintered friction materials are classified as metal— nonmetal combinations (49,50). These are best manufactured by the P/M process. Clutch plates, brake bands, brake blocks, and packing compositions are examples of friction materials (see Brake linings and clutch facings). [Pg.189]

Structure Modification. Several types of stmctural defects or variants can occur which figure in adsorption and catalysis (/) surface defects due to termination of the crystal surface and hydrolysis of surface cations (2) stmctural defects due to imperfect stacking of the secondary units, which may result in blocked channels (J) ionic species, eg, OH , AIO 2, Na", SiO , may be left stranded in the stmcture during synthesis (4) the cation form, acting as the salt of a weak acid, hydrolyzes in aqueous suspension to produce free hydroxide and cations in solution and (5) hydroxyl groups in place of metal cations may be introduced by ammonium ion exchange, followed by thermal deammoniation. [Pg.447]

Corrosion inhibitors are used to protect both the container and the metal substrate being stripped. Acid activated removers use inhibitors to block corrosion on active metals. Typical inhibitors are propylene oxide [75-56-9], butylene oxide [9106-88-7], triethylammonium phosphates, and sodium ben2oate [532-32-1] (see Corrosion and corrosion control). [Pg.551]

Calcium carbonate (calcite) scale formation in hard water can be prevented by the addition of a small amount of soluble polyphosphate in a process known as threshold treatment. The polyphosphate sorbs to the face of the calcite nuclei and further growth is blocked. Polyphosphates can also inhibit the corrosion of metals by the sorption of the phosphate onto a thin calcite film that deposits onto the metal surface. When the polyphosphate is present, a protective anodic polarization results. [Pg.340]


See other pages where Metallic block metals is mentioned: [Pg.98]    [Pg.2748]    [Pg.13]    [Pg.499]    [Pg.500]    [Pg.84]    [Pg.36]    [Pg.25]    [Pg.146]    [Pg.316]    [Pg.15]    [Pg.79]    [Pg.94]    [Pg.197]    [Pg.232]    [Pg.312]    [Pg.417]    [Pg.400]    [Pg.333]    [Pg.391]    [Pg.80]    [Pg.204]    [Pg.317]    [Pg.493]    [Pg.175]    [Pg.196]    [Pg.212]    [Pg.212]    [Pg.239]    [Pg.388]    [Pg.465]    [Pg.351]    [Pg.380]    [Pg.536]    [Pg.101]    [Pg.397]   
See also in sourсe #XX -- [ Pg.742 ]

See also in sourсe #XX -- [ Pg.855 ]

See also in sourсe #XX -- [ Pg.1003 ]




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