Big Chemical Encyclopedia

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

Articles Figures Tables About

Phosphoric acid molecule

This kind of ester acts as a nonionic surfactant if the alkanol groups contain hydrophilic moieties. If only two molecules of alkanoles are added to the phosphoric acid molecule an acid or secondary dialkyl phosphoric acid ester is formed that are an amphiphilic molecule by itself see Eq. (5). [Pg.555]

C04-0028. Write the net ionic reaction and draw a picture of the resulting anion when two hydroxide ions react with a phosphoric acid molecule. [Pg.241]

In particular, electron transfer results in that phosphoric acid molecules present in ATP, NADP and NADPN contain oxygen atoms in the form of O". Spatial-energy interactions (including isomorphic) are objectively expressed both at similar and opposite electrostatic charge of atoms-components. Such interactions can also take place between two heterogeneous atoms, if only their PE-parameters are roughly equal, and geometric shapes of orbitals are similar or alike. [Pg.98]

The two principal hallucinogenic constituents of psilocybe mushrooms (and related genera) are psilocybin and psilocin (Schultes and Hofman 1980,1992) (figure 9.4). They are very similar, having a dimethyltryptamine structure and differing only by a phosphoric acid molecule. Psilocybin may be called 4-phosphoryl-DMT and psilocin may be called 4-hydroxy DMT. They are both approximately 1/200 as potent as LSD. Absorption is adequate through the oral route, making this a common form of consumption. [Pg.355]

Phosphoric acid molecules can form acid-anhydride bonds with each other. It is therefore possible for two nucleotides to be linked via the phosphate residues. This gives rise to dinucleotides with a phosphoric acid-anhydride structure. This group includes the coenzymes NAD(P) " and CoA, as well as the flavin derivative FAD (1 see p. 104). [Pg.80]

Interaction of the two forms, either on the same phosphoric acid molecule or on two adjacent molecules, yields the polymer ... [Pg.54]

Pure phosphoric acid is a colourless crystalline solid (m.p. 42.35°C) and it is usually employed in solution as a strong syrupy liquid, miscible in all proportions with water. It is commercially available in solution concentrations of 75, 80 and 90%. The syrupy nature of its solution occurs at concentrations greater than 50% and is the result of hydrogen bonding between the phosphoric acid molecules. [Pg.102]

Determine the molecular structure and the hybridization of the central atom of the phosphoric acid molecule. [Pg.906]

In the phosphoric acid molecule the hydrogen atoms are attached to the oxygen atoms. The Lewis structure is shown below. Note that the phosphorus atom is surrounded by four effective pairs, which are arranged tetrahedrally. The atom is described as sp3 hybridized. [Pg.907]

The Condensed Phosphoric Acids. Phosphoric acid easily undergoes the process of condensation. Condensation is the reaction of two or more molecules to form larger molecules, either without any other products (in which case the condensation is also called polymerization), or with the elimination of small molecules, such as water. Condensation of two phosphoric acid molecules occurs by the reaction of two... [Pg.451]

Neither pure supercritical CO2 nor ethanol-modified CO2 eluted all the flavonoids tested in this experiment. But when phosphoric acid and ethanol modifiers were added to the mobile phase together, the separation on a silica-based column was significantly improved, and quercetin and risetin were eluted rapidly and efficiently. With an increase of phosphoric acid concentration, the peak shapes were also improved. Because the phosphoric acid molecules could be adsorbed onto the active sites of the stationary phase, which could prevent solute molecules from being strongly adsorbed, the interaction between solutes and stationary phase was eliminated, making the solutes easily elute from the chromatographic system. [Pg.687]

Check to see that the reaction occurs through hydrogen ion transfer from phosphoric acid molecules to hydroxide ions. Every weak acid-strong base reaction occurs by this type of H+ transfer. [Pg.529]

Diphosphoric acid is formed by dehydration between pairs of phosphoric acid molecules. The oxygen linkage between the two phosphate units is an anhydride linkage ... [Pg.308]

Unlike other acids, in concentrated phosphoric acid solutions (where the water concentration is low) hydrogen ions exist not as hydrated ions H+ H20, but as ions solvated by phosphoric acid molecules H+ - H3P04. For this reason, the solution s conductivity is a complex, nonmonotonous function of concentration. As for the conductivity mechanism, these ions do not move like a spherical particle in a viscous medium when an electric field is applied to the solution (the Stokes mechanism), but rather the protons alone jump in the field direction from one acid molecule to another acid molecule (the Grotthuss mechanism, suggested in 1806 as an explanation for the conductivity behavior in aqueous solutions). [Pg.214]

PBI films doped with phosphoric acid were prepared by immersion of PBI films in aqueous solutions of phosphoric acid for at least 16 h [181-185]. Upon equilibration in a 11 M H3PO4 solution a doping level of 5 phosphoric acid molecules per repeating unit of the polymer was achieved. [Pg.121]

In the crown ether complex 2H3P04 (C,2H2406)-61120, the phosphoric acid molecules form H bonded dimers which are also H bond linked through the water molecules to the O atoms in the ether rings. The dimers lie outside the ether rings and are each linked to four different rings by the complex H bond system which is present. [Pg.1252]

The conduction mechanism is substantiated through the proton transfer/hopping between a proton donor and a proton acceptor in combination to the ability of the proton carrier (positive ion) to rotate and move so that it will transfer the proton to a negative ion according to reaction (2). As reported by Ma et al., the immobiU-zation of phosphoric acid molecules in the flame of the polymer membrane chains results in proton conductivity values one order of magnitude below the corresponding proton conductivity of pure phosphoric acid. [Pg.348]

Several materials have been proposed and commercialized as electrolytes for HT-PEFCs. As introduced before, the main polymers used materials from the PBI family and the Advent tetramethyl pyridine sulfone (TPS) family, both being basic polymers allowing chemical interaction with mineral acids (e.g., phosphoric acid) see Fig. 1. Differences can be fotmd both in the chemistry and in the synthetic process especially among the different PBIs, yielding different physicochemical properties such as glass transition temperatures, mechanical stabilities, proton conductivities, and achievable phosphoric acid doping levels (defined as either the ratio of phosphoric acid molecules per polymer repeat unit or the weight ratio of polymer and included phosphoric acid) for a summary, see Table 1. [Pg.997]

EXERCISE 9.15 Write the Lewis formula that best describes the phosphoric acid molecule, H3PO4. [Pg.358]

Thus, H4PO4 is more acidic than H3O and more energy (0.30 eV) is needed for transfer of a proton from one phosphoric acid molecule to another. [Pg.41]

The term acid doping level (ADL) is widely used and is defined as the number of phosphoric acid molecules per polymer repeat unit and can be calculated according to (6.14), where Mpbi is the molar mass of the polymer repeat xmit and MpA is the molar mass of PA. [Pg.132]


See other pages where Phosphoric acid molecule is mentioned: [Pg.104]    [Pg.218]    [Pg.1056]    [Pg.171]    [Pg.72]    [Pg.1044]    [Pg.204]    [Pg.323]    [Pg.1057]    [Pg.636]    [Pg.308]    [Pg.349]    [Pg.357]    [Pg.391]    [Pg.255]    [Pg.1063]    [Pg.396]    [Pg.450]    [Pg.41]    [Pg.42]    [Pg.50]    [Pg.55]    [Pg.60]    [Pg.60]    [Pg.60]    [Pg.114]    [Pg.115]   
See also in sourсe #XX -- [ Pg.492 ]




SEARCH



© 2024 chempedia.info