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Direct charges

The device operates as described below. After switching on the power source, CB begins to be charged from Ac. CS provides direct charging current of 0.1 A that makes it possible not to exceed Ac permissible discharging current value as well as to minimize CB charging time till approximately 10s. [Pg.651]

Direct costs are those that can be directly charged to a single product. The most obvious direc t cost is for raw materials, of which the quantity consumed is directly proportional to the amount of product manufactured. Direct process labor is also considered to be a direct cost. [Pg.846]

However, many costs cannot be directly charged to an individual produc t. These so-called indirect, burden, or overhead costs range From the lighting and heating required for the plant and offices to the cafeteria and medical facihties provided. When several products are made in a plant, it becomes increasingly difficult to allocate overheads correctly among the various products. [Pg.846]

Chemical reactions, which involve direct charge transfer between the metal atom in the lattice of the metal and the oxidising species. [Pg.19]

Insulators After mixing with conductor After mixing with conductor Directly Charge compensation... [Pg.649]

Fig. 3 Transient spectra obtained upon the application of a 200-fs laser pulse to a solution of stilbene (S) and chloranil (Q) in dioxane. (a) The fast decay ( 20 ps) of the contact ion-radical pair S+ , Q generated by direct charge-transfer excitation (CT path), (b) The slow growth ( 1.6 ns) of the ion pair S+ Q due to the diffusional quenching of triplet chloranil (A path) as described in Scheme 13. Reproduced with permission from Ref. 55. Fig. 3 Transient spectra obtained upon the application of a 200-fs laser pulse to a solution of stilbene (S) and chloranil (Q) in dioxane. (a) The fast decay ( 20 ps) of the contact ion-radical pair S+ , Q generated by direct charge-transfer excitation (CT path), (b) The slow growth ( 1.6 ns) of the ion pair S+ Q due to the diffusional quenching of triplet chloranil (A path) as described in Scheme 13. Reproduced with permission from Ref. 55.
Including 20 ft2 for miscellaneous items not identified in this section, 110.3 ft2 must be rented, at an annual cost of 44,100/yr. Note that this moderately sized complex is added to an existing electronic materials manufacturing facility. Hence, no direct charges are added for infrastructure, such as non-clean room and office space. The total purchase cost, 6,492,100, provides equipment modules that require small installation costs, on the order of 1% that is, 65,000. Note also that two PECVD reactors are provided to assure uninterrupted operation when the plant is in operation, around the clock, 330 day/yr. While the robot loads and unloads one of the reactors, the other reactor is in operation. [Pg.307]

Dispersions of fine mineral particles can be stabilised by direct electrical charging of the particles or by steric/electrosteric protection from adsorbed polymers. Stabilisation by direct charging is well described by the classical DLVO theory. ... [Pg.6]

Why was defence expenditure a prominent target for economies from the mid-1950s The most obvious reason was that military personnel had to be maintained abroad and were a direct charge on the United Kingdom balance of payments. As table 6.4 shows, there was a marked reduction in the numbers of personnel overseas between 1955 and the... [Pg.304]

Phenothiazine (PTZ) and ferrocene (Fc), both of which have a small reorganization energy associated to the electron transfer, are the first comediators that have been considered. Each has a potential that falls between 0.22 and 0.75 V versus SCE, respectively, the potential of the Co(DTB)33+/2+ and of the dye [Ru(H2DCB)-(dnbpy)(NCS)2]+/0. Because of the facile electron transfer, the photooxidized dye would be predominantly reduced by the comediator. Its oxidized form (PTZ+ and Fc +) can then be rapidly intercepted by Co(II), preventing the direct charge recombination between the oxidized comediator and the electrons in the 2. Nanosecond... [Pg.551]

Thus hole or electron transfer can follow a number of pathways across the semiconductor/electrolyte interface. First, one can have direct oxidative or reductive charge transfer to solution species resulting in desired product formation. Second, one can have direct charge transfer resulting in surface modification, such as oxide film growth on GaP or CdS in aqueous PECs. Finally, one can have photoemission of electrons or holes directly into the electrolyte. All of these processes provide some information about the electronic structure of the interface. [Pg.88]

Neutral alumina (1.5 g) was thoroughly mixed with iodobenzene diacetate (532 mg, 1.65 mmol) and benzyl phenyl sulfide Id (300 mg, 1.5 mmol) using a pestle and mortar. The adsorbed material was placed in an alumina bath inside the microwave oven and irradiated at 50% power for two successive intervals of 45 s each (with time interval of 3-4 min bath temperature rose to 80-85 °C). The progress of the reaction was monitored by TLC (hexane-ethyl acetate, 7 3, v/v). When the reaction was complete the whole material was directly charged onto a silica gel column which provided iodobenzene on elusion with hexane (100 mL). The fractions eluted by chloroform-hexane (1 1 v/v) provided sulfone (<7% by... [Pg.36]

A mixture of benzaldehyde 2a (1.6 g, 10 mmol), cyclohexa-l,4-dione 1 (1.12 g, 10 mmol) and 37% w/w KF-A1203 (3 wt. equiv. of aldehyde) was placed in a Pyrex test tube and subjected to microwave irradiation at an output of 600 W. After completion of the reaction (3 min) as indicated by TLC, the reaction mass was cooled to room temperature, directly charged on a silica gel column (100-200 mesh) and eluted (ethyl acetate-hexane, 3 7) to afford 2-benzylhydroquinone 3a as a white crystalline solid (1.7 g, 85%). [Pg.103]

Dimetlioxybenzene la (5 mmol), diethyl azodicarboxylate (5 mmol) and InCl3-Si02 (3 wt equiv. of arene) were admixed in an Erlenmeyer flask and exposed to microwave irradiation at 450 W using BPL, BMO-700 T focused micro-wave oven for 3 min (pulsed irradiation 1 min with 20 s interval). On completion, the reaction mixture was directly charged on a small silica gel column and eluted with a mixture of ethyl acetate-hexane (2 8) to afford pure hydrazine 2a in 88% yield as a pale yellow solid. [Pg.259]

Ea of 0.01 V/ftm is then applied. This is required for two reasons to induce directional charge transport along the wavevector axis, and due to the collective orientational response that produces the index of refraction change. In other words, the applied field, which is greater in magnitude than the internal space-charge field, is required to keep the modulation of the internal electric field... [Pg.323]


See other pages where Direct charges is mentioned: [Pg.165]    [Pg.327]    [Pg.186]    [Pg.117]    [Pg.93]    [Pg.272]    [Pg.417]    [Pg.418]    [Pg.427]    [Pg.445]    [Pg.256]    [Pg.75]    [Pg.70]    [Pg.257]    [Pg.403]    [Pg.83]    [Pg.56]    [Pg.275]    [Pg.82]    [Pg.649]    [Pg.153]    [Pg.199]    [Pg.152]    [Pg.229]    [Pg.254]    [Pg.244]    [Pg.313]    [Pg.102]    [Pg.325]    [Pg.193]    [Pg.200]    [Pg.463]    [Pg.20]    [Pg.132]   
See also in sourсe #XX -- [ Pg.116 ]




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