Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Subject 2-oxide

Gases which are high in FIjS are subject to a de-sulphurisation process in which H2S is converted into elemental sulphur or a metal sulphide. There are a number of processes based on absorption in contactors, adsorption (to a surface) in molecular sieves or chemical reaction (e.g. with zinc oxide). [Pg.254]

Many solids have foreign atoms or molecular groupings on their surfaces that are so tightly held that they do not really enter into adsorption-desorption equilibrium and so can be regarded as part of the surface structure. The partial surface oxidation of carbon blacks has been mentioned as having an important influence on their adsorptive behavior (Section X-3A) depending on conditions, the oxidized surface may be acidic or basic (see Ref. 61), and the surface pattern of the carbon rings may be affected [62]. As one other example, the chemical nature of the acidic sites of silica-alumina catalysts has been a subject of much discussion. The main question has been whether the sites represented Brpnsted (proton donor) or Lewis (electron-acceptor) acids. Hall... [Pg.581]

A large variety of organic oxidations, reductions, and rearrangements show photocatalysis at interfaces, usually of a semiconductor. The subject has been reviewed [326,327] some specific examples are the photo-Kolbe reaction (decarboxylation of acetic acid) using Pt supported on anatase [328], the pho-... [Pg.738]

The carriers in tire channel of an enhancement mode device exhibit unusually high mobility, particularly at low temperatures, a subject of considerable interest. The source-drain current is carried by electrons attracted to tire interface. The ionized dopant atoms, which act as fixed charges and limit tire carriers mobility, are left behind, away from tire interface. In a sense, tire source-drain current is carried by tire two-dimensional (2D) electron gas at tire Si-gate oxide interface. [Pg.2892]

Dichlorine h ptoxide, CljO, is the most stable of the chlorine oxides. It is a yellow oil at room temperature, b.p. 353 K, which will explode on heating or when subjected to shock. It is the anhydride of chloric(VlI) acid (perchloric acid) from which it is prepared by dehydration using phosphorus(V) oxide, the acid being slowly reformed when water is added. [Pg.336]

When an aromatic compound having an aliphatic side chain is subjected to oxidation, fission of the side chain occurs between the first and second carbon atoms from the benzene ring, the first carbon atom thus becoming part of a carboxyl ( -COOH) group. For example ... [Pg.239]

Chloroanisole and p-nitrophenol, the nitrations of which are susceptible to positive catalysis by nitrous acid, but from which the products are not prone to the oxidation which leads to autocatalysis, were the subjects of a more detailed investigation. With high concentrations of nitric acid and low concentrations of nitrous acid in acetic acid, jp-chloroanisole underwent nitration according to a zeroth-order rate law. The rate was repressed by the addition of a small concentration of nitrous acid according to the usual law rate = AQ(n-a[HN02]atoioh) -The nitration of p-nitrophenol under comparable conditions did not accord to a simple kinetic law, but nitrous acid was shown to anticatalyse the reaction. [Pg.58]

Subject Phenyl acetones by electrolytic oxidation From "guest" ... [Pg.189]

Type J thermocouples (Table 11.58) are one of the most common types of industrial thermocouples because of the relatively high Seebeck coefficient and low cost. They are recommended for use in the temperature range from 0 to 760°C (but never above 760°C due to an abrupt magnetic transformation that can cause decalibration even when returned to lower temperatures). Use is permitted in vacuum and in oxidizing, reducing, or inert atmospheres, with the exception of sulfurous atmospheres above 500°C. For extended use above 500°C, heavy-gauge wires are recommended. They are not recommended for subzero temperatures. These thermocouples are subject to poor conformance characteristics because of impurities in the iron. [Pg.1216]

Sample Preservation Without preservation, many solid samples are subject to changes in chemical composition due to the loss of volatile material, biodegradation, and chemical reactivity (particularly redox reactions). Samples stored at reduced temperatures are less prone to biodegradation and the loss of volatile material, but fracturing and phase separations may present problems. The loss of volatile material is minimized by ensuring that the sample completely fills its container without leaving a headspace where gases can collect. Samples collected from materials that have not been exposed to O2 are particularly susceptible to oxidation reactions. For example, the contact of air with anaerobic sediments must be prevented. [Pg.198]

Although thiosulfate is one of the few reducing titrants not readily oxidized by contact with air, it is subject to a slow decomposition to bisulfite and elemental sulfur. When used over a period of several weeks, a solution of thiosulfate should be restandardized periodically. Several forms of bacteria are able to metabolize thiosulfate, which also can lead to a change in its concentration. This problem can be minimized by adding a preservative such as Hgl2 to the solution. [Pg.344]

A second degradation process is oxidation, often photo-induced especially by exposure to light not filtered for uv. The radicals resulting from this reaction promote depolymerization of the cellulose, as well as yellowing and fa ding of paper and media. Aging causes paper to become more crystalline and fragile, and this can be exacerbated particularly if the paper is subjected to poor conditions. [Pg.428]


See other pages where Subject 2-oxide is mentioned: [Pg.156]    [Pg.403]    [Pg.403]    [Pg.110]    [Pg.97]    [Pg.156]    [Pg.403]    [Pg.403]    [Pg.110]    [Pg.97]    [Pg.439]    [Pg.440]    [Pg.484]    [Pg.713]    [Pg.2614]    [Pg.2725]    [Pg.2732]    [Pg.311]    [Pg.889]    [Pg.146]    [Pg.3]    [Pg.67]    [Pg.92]    [Pg.221]    [Pg.343]    [Pg.24]    [Pg.43]    [Pg.251]    [Pg.351]    [Pg.10]    [Pg.58]    [Pg.79]    [Pg.164]    [Pg.169]    [Pg.235]    [Pg.243]    [Pg.244]    [Pg.165]    [Pg.246]    [Pg.246]    [Pg.309]    [Pg.369]    [Pg.427]    [Pg.36]   


SEARCH



1,2,5-Oxadiazole 2-oxide Subject

Cumulative Subject allylic oxidation

Cumulative Subject oxidants

Cumulative Subject oxidation

Cumulative Subject oxidative rearrangement

Cumulative Subject oxide

Dichlorine oxide Subject

Electrochemical oxidation Subject

Furan, 2,5-dimethoxy-2,5-dihydroSubject allylic oxidation

Furan, 2,5-dimethoxy-2,5-dihydroSubject oxidation

Glycols, oxidation Subject

Graphene oxide Subject

Graphite oxides Subject

Heteroatom oxidations Subject

Iron oxide hydroxides Subject

Lithium oxide Subject

Metal oxides Subject

Nitric oxide synthase Subject

Oppenauer oxidation Subject

Oxidants Subject

Oxidation General Subject

Oxidative bleaching Subject

Oxidative cyclization Subject

Oxidative decarboxylation 382 Subject

Oxide films Subject

Oxides, electrode/solution interface 424 Subject

Periodate, acidic, oxidation with Subject

Polyethylene oxide Subject

SUBJECTS compounds 718, oxide

Selective oxidations Subject

Silver oxide Subject

Subject Oxidative elimination

Subject alcohol oxidation

Subject allene oxides

Subject allylic oxidation

Subject carbon oxides

Subject copper oxide

Subject dioxirane oxidation

Subject in allylic oxidation

Subject index oxidation

Subject nitrous oxide

Subject oxidation

Subject oxidation

Subject oxidation process

Subject oxidation rates

Subject oxidation states

Subject oxidation with

Subject oxidation/reduction

Subject oxidative addition

Subject oxidative cleavage

Subject oxidative rearrangement

Subject oxidative stress

Subject oxide glasses

Subject oxide halides

Subject phosphine oxides

Subject phosphorus oxides

Subject pyridine oxides

Subject selenium oxides

Subject sulfur oxides

Subject transition metal oxides

Thiophene oxides Subject

Zinc oxide Subject

© 2024 chempedia.info