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In the last years one can find a strong reorientation of most microscopical methods to study objects in natural (or adjustable) conditions without preparation. Microscopical visualization without vacuum and coating allows maintaining the natural specimen structure as well as examining its behavior under external influences (loading, chemical reactions, interaction with other solids, liquids, gases etc.)... [Pg.579]

Finite difference techniques are used to generate molecular dynamics trajectories with continuous potential models, which we will assume to be pairwise additive. The essential idea is that the integration is broken down into many small stages, each separated in time by a fixed time 6t. The total force on each particle in the configuration at a time t is calculated as the vector sum of its interactions with other particles. From the force we can determine the accelerations of the particles, which are then combined with the positions and velocities at a time t to calculate the positions and velocities at a time t + 6t. The force is assumed to be constant during the time step. The forces on the particles in their new positions are then determined, leading to new positions and velocities at time t - - 2St, and so on. [Pg.369]

Most of the modeling methods discussed in this text model gas-phase molecular behavior, in which it is reasonable to assume that there is no interaction with other molecules. However, most laboratory chemistry is done in solution where the interaction between the species of interest and the solvent is not negligible. [Pg.206]

The molecular dynamics method is useful for calculating the time-dependent properties of an isolated molecule. However, more often, one is interested in the properties of a molecule that is interacting with other molecules. With HyperChem, you can add solvent molecules to the simulation explicitly, but the addition of many solvent molecules will make the simulation much slower. A faster solution is to simulate the motion of the molecule of interest using Langevin dynamics. [Pg.91]

T ablation temperature No general trend. Depends on interaction with other parameters and design criteria. None except as an indicator of whether or not ablation will occur. [Pg.2]

Practically all lubricating oils contain at least one additive some oils contain several. The amount of additive that is used varies from < 0.01 to 30% or more. Additives can have detrimental side effects, especially if the dosage is excessive or if interactions with other additives occur. Some additives are multifimctional, eg, certain VI improvers also function as pour-point depressants or dispersants. The additives most commonly used in hydrautic fluids include pour-point depressants, viscosity index improvers, defoamers, oxidation inhibitors, mst and corrosion inhibitors, and antiwear compounds. [Pg.265]

Crystallinity of polypropylene is usually determined by x-ray diffraction (21). Isotactic polymer consists of heHcal molecules, with three monomer units pet chain unit, resulting in a spacing between units of identical conformation of 0.65 nm (Fig. 2a). These molecules interact with others, or different... [Pg.407]

Typical cosolvents include methanol [67-56-17, ethanol [64-17-5] isopropyl alcohol [67-65-OJ, or toluene. The selection of cosolvents depends on the requirement of the formula and their interaction with other ingredients. Methanol is a common cosolvent in methylene chloride formulas since it has good solvency and is needed to swell ceUulose-type thickening agents. A typical methylene chloride formula used to strip wood is as follows (7). [Pg.551]

Teratogenic effects have been noted with 2- and 4-aminophenol in the hamster, but 3-aminophenol was without effect in the hamster and rat (129,130). 4-Aminophenol is known to inhibit DNA synthesis and alter DNA stmcture in human lymphoblasts (131,132) and is mutagenic in mouse micronuclei tests (133). The aminophenols have been shown to be genotoxic, as evidenced by the induction of sister chromatid exchanges (134,135), but they also exert a protective effect against DNA interaction with other noxious chemicals (136). After assessment of available data a recent report stated that the aminophenols were safe as cosmetic ingredients in their present uses and concentrations (137). [Pg.312]

Pauli proposed that two particles were emitted, and Fermi called the second one a neutrino, V. The complete process therefore is n — p -H e 9. Owing to the low probabiHty of its interacting with other particles, the neutrino was not observed until 1959. Before the j3 -decay takes place there are no free leptons, so the conservation of leptons requires that there be a net of 2ero leptons afterward. Therefore, the associated neutrino is designated an antineutrino, 9-, that is, the emitted electron (lepton) and antineutrino (antilepton) cancel and give a net of 2ero leptons. [Pg.448]

Polymerization and depolymerization of sihcate anions and their interactions with other ions and complexing agents are of great interest in sol—gel and catalyst manufacture, detergency, oil and gas production, waste management, and limnology (45—50). The complex silanol condensation process may be represented empirically by... [Pg.6]

Toxicological studies have demonstrated that there are no important problems with fluconazole. Therapeutic doses of fluconazole may cause enzyme induction in the Hver. This suggests that interactions with other dmgs cannot be excluded. The side effects are similar to those of itraconazole and include nausea, headache, and vertigo. Occasionally, increased Hver enzymes may be noted. Like itraconazole, fluconazole is contraindicated during pregnancy. [Pg.257]

An abrasive is usually chemically inert, neither interacting with other dentifrice ingredients nor dissolving in the paste or the mouth. Substances used as dentifrice abrasives include amorphous hydrated silica, dicalcium phosphate dihydrate [7789-77-7] anhydrous dicalcium phosphate [7757-93-9] insoluble sodium metaphosphate [10361-03-2], calcium pyrophosphate [35405-51-7], a-alumina trihydrate, and calcium carbonate [471-34-1]. These materials are usually synthesized to specifications for purity, particle size, and other characteristics naturally occurring minerals are used infrequently. Sodium bicarbonate [144-55-8] and sodium chloride [7647-14-5] have also been employed as dentifrice abrasives. [Pg.501]


See other pages where Interactions with other is mentioned: [Pg.245]    [Pg.80]    [Pg.308]    [Pg.1463]    [Pg.1554]    [Pg.2816]    [Pg.186]    [Pg.394]    [Pg.318]    [Pg.351]    [Pg.418]    [Pg.611]    [Pg.13]    [Pg.102]    [Pg.367]    [Pg.1047]    [Pg.125]    [Pg.438]    [Pg.610]    [Pg.201]    [Pg.314]    [Pg.475]    [Pg.43]    [Pg.47]    [Pg.47]    [Pg.411]    [Pg.209]    [Pg.346]    [Pg.369]    [Pg.531]    [Pg.449]    [Pg.244]    [Pg.146]    [Pg.2146]    [Pg.7]    [Pg.212]    [Pg.54]    [Pg.7]   
See also in sourсe #XX -- [ Pg.179 ]




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Alprazolam interaction with other drugs

Aminoglycoside antibiotics interaction with other drugs

Amphetamines interaction with other drugs

Amphotericin interaction with other drugs

Anaesthesia interactions with other drugs

Anticonvulsants interaction with other drugs

Antidepressants interaction with other drugs

Anxiolytics, other Interactions with

Benzodiazepines interaction with other drugs

Beta blockers interaction with other drugs

Boronic acids combination with other interactions

Bupropion interaction with other drugs

Buspirone interaction with other drugs

CSN-subunit Interactions With Other Proteins

Caffeine interaction with other drugs

Carbamazepine interaction with other drugs

Central nervous system depressants alcohol interacting with other

Cephalosporins interaction with other drugs

Chloramphenicol interaction with other drugs

Cimetidine interaction with other drugs

Ciprofloxacin interaction with other drugs

Citalopram interaction with other drugs

Clonidine interaction with other drugs

Clozapine interaction with other drugs

Contraceptives interaction with other drugs

Cyclosporine interaction with other drugs

Diazepam interactions with other drugs

Diltiazem interaction with other drugs

Disulfiram interaction with other drugs

Drug failure interactions with other drugs

Erythromycin drug interactions with other drugs

Erythromycin interaction with other drugs

Estrogen interaction with other drugs

Flavor compounds, interactions with other food components

Fluoxetine interaction with other drugs

Fluvoxamine interaction with other drugs

Gabapentin interaction with other drugs

Guanethidine interaction with other drugs

Haloperidol interaction with other drugs

Health effects interactions with other nutrients

Hydrogen Bonding with Other Noncovalent Interactions

Hypoglycemic agents, oral, interaction with other drugs

Imipramine interaction with other drugs

Immunoglobulins interactions with other

Insulin interaction with other drugs

Interaction Properties with Other Polysaccharides

Interaction with Other Additives

Interaction with Other Surfactant

Interaction with other drugs

Interactions of Ions with Other Solutes

Interactions with Other Compounds

Interactions with Other Food Components

Interactions with Other Food Constituents

Interactions with other metals

Interactions with other plant allelochemicals

Iron interactions with other metals

Isoniazid interaction with other drugs

Itraconazole interaction with other drugs

Ketoconazole interaction with other drugs

Lamotrigine interaction with other drugs

Levodopa interaction with other drugs

Lithium interaction with other drugs

Macrolide antibiotic interaction with other drugs

Methadone interaction with other drugs

Methylphenidate interaction with other drugs

Metronidazole interaction with other drugs

Mirtazapine interaction with other drugs

Monoamine oxidase inhibitors interaction with other drugs

Nefazodone interaction with other drugs

Neonicotinoids interaction with other

Nitrates interaction with other drugs

Omeprazole interaction with other drugs

Oxcarbazepine interaction with other drugs

Paroxetine interaction with other drugs

Pectin interactions with other biopolymers

Penicillin interaction with other drugs

Pharmacological Interactions Between Antiretrovirals and Other Medications with Activity in the Central Nervous System

Phenothiazines interaction with other drugs

Phenytoin interaction with other drugs

Polymer stabilization interactions with other additives

Propranolol interaction with other drugs

Purchasing interaction with other functions

Quinidine interaction with other drugs

Rifampin interaction with other drugs

Risperidone interaction with other drugs

Sedative medications interaction with other drugs

Serotonin reuptake inhibitors, selective interaction with other drugs

Sertraline interaction with other drugs

Sibutramine interaction with other drugs

Sulfonamides interaction with other drugs

Tetracycline interaction with other drugs

Theophylline interaction with other drugs

Thioridazine interaction with other drugs

Through-bond interactions with other nuclei

Thyroid hormones interaction with other drugs

Tricyclic antidepressants interaction with other drugs

Valproic acid interaction with other drugs

Venlafaxine interaction with other drugs

Verapamil interaction with other drugs

Warfarin interaction with other drugs

Water interaction with other molecules

Xylans interaction with other polysaccharide

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