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Solubilisation

One of the most important characteristics of micelles is their ability to take up all kinds of substances. Binding of these compounds to micelles is generally driven by hydrophobic and electrostatic interactions. The dynamics of solubilisation into micelles are similar to those observed for entrance and exit of individual surfactant molecules. Their uptake into micelles is close to diffusion controlled, whereas the residence time depends on the sttucture of the molecule and the solubilisate, and is usually in the order of 10 to 10 seconds . Hence, these processes are fast on the NMR time scale. [Pg.127]

Solubilisation is usually treated in terms of the pseudophase model, in which the bulk aqueous phase is regarded as one phase and tire micellar pseudophase as another. This allows the affinity of the solubilisate for the micelle to be quantified by a partition coefficient P. Different definitions of P can be found in the literature, differing in their description of the micellar phase. Frequently P is [Pg.127]

The unexpected preference for the interfacial region at lower concentrations of benzene has prompted speculation. It has been demonstrated that aromatic compounds are capable of forming weak hydrogen bonds with water. This ability favours uptake in the aqueous interface over solubilisation in the interior. Alternatively, some authors have attributed the binding behaviour of benzene to its [Pg.128]

The binding behaviour of benzene can be extrapolated to many other aromatic compounds such as naphthalene and benzene derivativesInterestingly, a large number of probe molecules contain aromatic rings and many of them will prefer the outer regions of micelles, whereas in bilayer systems, the same molecules prefer the interior of the aggregate . Qearly these probes cannot be used to determine polarity of the micellar interior or the extent of water penetration therein . [Pg.129]

For ammonium surfactants there is evidence for the existence of an additional specific interaction between the headgroups of the surfactant and the aromatic solubilisate . This is in line with the observation that partition coefficients for benzene in CTAB solutions are much higher than those for [Pg.129]

Freeze-thawing - adlib All, esp. animal and plant tissue [Pg.55]

Hypotonic shock Water adlib Animal and plant tissue esp. erythrocytes and reticulocytes [Pg.55]

Enzymatic lysis Lysozyme/Triton X-100 100 ml Gram-positive bacteria [Pg.55]

Many membrane proteins, or proteins that have a tendency to aggregate, can be stabilised effectively in buffer solutions containing glycerol (5-25%). Higher concentrations of glycerol are useful for storing protein in liquid state in the freezer (-20 °C) or in the ultra-cold freezer (-80 °C). [Pg.56]


Detergents are made by, for example, treating petroleum hydrocarbons with sulphuric acid, yielding sulphonated products which are water soluble. These can also solubilise fats and oils since, like the stearate ion, they have an oil-miscible hydrocarbon chain and a water-soluble ionic end. The calcium salts of these substances, however, are soiu u-ic in water and, therefore, remove hardness without scum formation. [Pg.273]

Calculations usirig this value afford a partition coefficient for 5.2 of 96 and a micellar second-order rate constant of 0.21 M" s" . This partition coefficient is higher than the corresponding values for SDS micelles and CTAB micelles given in Table 5.2. This trend is in agreement with literature data, that indicate that Cu(DS)2 micelles are able to solubilize 1.5 times as much benzene as SDS micelles . Most likely this enhanced solubilisation is a result of the higher counterion binding of Cu(DS)2... [Pg.144]

In retrospect, this study has demonstrated the limitations of two commonly accepted methods of analysing solubilisation and micellar catalysis, respectively. It has become clear that solubilisate ririg-current induced shifts need to be interpreted with due caution. These data indicate a proximity of solubilisate and parts of the surfactant and, strictly, do not specify the location within the micelle where the encounter takes place. Also the use of the pseudophase model for bimolecular reactions requires precaution. When distribution of the reactants over the micelle is not comparable, erroneous results are likely to be obtained... [Pg.153]

Sulfonates. The sulfonate group, -SO M, attached to an alkyl, aryl, or alkylaryl hydrophobe, is a highly effective solubilising group. Sulfonic acid... [Pg.239]

PhenoHc dispersions made using natural soaps are sensitive to hard water, but under proper formulation they can tolerate water of 400 ppm total hardness and maintain complete clarity and germicidal activity. The highest activity for phenols was found when using secondary alkane sulfonates as solubilising agents (75). [Pg.125]

Surfactants in E/ectroc/eaners. Surfactants typically consist of a long-chain hydrocarbon molecule having a solubilising or water-loving group which can be anionic, cationic, or nonionic when solubilized. Thousands of surfactant products are marketed, usually under trade names (32). In commercially formulated electrocleaners, surfactants are usually anionic, and often mixtures of anionics and nonionics. [Pg.149]

For fluorescence PAH determination in tap water acid-induced cloud point extraction was used. This kind of extraction based on the phase separation into two isotropic liquid phases a concentrated phase containing most of the surfactant (surfactant-rich phase), where the solubilised solutes are exttacted, and an aqueous phase containing a surfactant concenttation closes to the critical micellar concentration. [Pg.116]

EC 1.9.3.1]. Purified by selective solubilisation with Triton X-1(X) and subsequently with lauryl maltoside finally by sucrose gradient centrifugation [Li et al. Biochem J 242 417 1978]. [Pg.526]

Histones (from S4A mouse lymphoma). Purification used a macroprocess column, heptafluorobutyric acid as solubilising and ion-pairing agent and an acetonitrile gradient. [McCroskey et al. Anal Biochem 163 427 1987.]... [Pg.541]

Reverse transcriptase (from avian or murine RNA tumour viruses) [9068-38-6] [EC 2.7.7.49]. Purified by solubilising the virus with non-ionic detergent. Lysed virions were adsorbed on DEAE-cellulose or DEAE-Sephadex columns and the enzyme eluted with a salt gradient, then chromatographed on a phosphocellulose column and enzyme activity eluted in a salt gradient. Purified from other viral proteins by affinity chromatography on a pyran-Sepharose column. [Verna Biochim Biophys Acta 473 1 7977 Smith Methods Enzymol 65 560 1980 see commercial catalogues for other transcriptases.]... [Pg.564]

In addition to stabilisers, antioxidants and ultra-violent absorbers may also be added to PVC compounds. Amongst antioxidants, trisnonyl phenyl phosphite, mentioned previously, is interesting in that it appears to have additional functions such as a solubiliser or chelator for PVC insoluble metal chlorides formed by reaction of PVC degradation products with metal stabilisers. Since oxidation is both a degradation reaction in its own right and may also accelerate the rate of dehydrochlorination, the use of antioxidants can be beneficial. In addition to the phenyl phosphites, hindered phenols such as octadecyl 3-(3,5-di-tcrt-butyl-4-hydroxyphenyI)propionate and 2,4,6-tris (2,5-di-rcrt-butyl-4-hydroxybenzyl)-1,3,5-trimethylbenzene may be used. [Pg.330]

The weathering process which eventually reduces the rock of the parent material to the inorganic constituents of soil comprises both physical and chemical changes. Size reduction from rocks to the colloidal state depends not only upon the mechanical action of natural forces but also on chemical solubilisation of certain minerals, action of plant roots, and the effects of organic substances formed by biological activity. [Pg.377]

Nicolas, M. T. (1980). Solubilisation du systeme lumineux des Polynoi niens, comparaison de differents tests d activite. Biol. Cellulaire 39 5. [Pg.423]


See other pages where Solubilisation is mentioned: [Pg.273]    [Pg.18]    [Pg.127]    [Pg.127]    [Pg.128]    [Pg.128]    [Pg.128]    [Pg.128]    [Pg.134]    [Pg.145]    [Pg.146]    [Pg.147]    [Pg.148]    [Pg.152]    [Pg.152]    [Pg.153]    [Pg.154]    [Pg.178]    [Pg.233]    [Pg.233]    [Pg.257]    [Pg.503]    [Pg.526]    [Pg.553]    [Pg.554]    [Pg.568]    [Pg.572]    [Pg.572]    [Pg.414]    [Pg.791]    [Pg.961]    [Pg.344]    [Pg.242]   
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See also in sourсe #XX -- [ Pg.166 ]

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Carboxylic acids solubilising

Cyclodextrins as solubilising agents

Emulsification solubilisation

Essential oils, solubilisation

Experimental Methods of Studying Solubilisation

Factors affecting solubilisation

Film and Solubilisation Theories of Microemulsions

Hydrotropic solubilisation

Lignin solubilisation

Micellar solubilisation

Micelles solubilisate location

Mixed Film and Solubilisation Theories of Microemulsions

Oral liquids solubilisates

Oral solubilisates

Pharmaceutical Aspects of Solubilisation

Pharmaceutical applications of solubilisation

Phase diagrams solubilised systems

Phenolic compounds, solubilised

SOLUBILISATION OF CNTs

Solubilisation Solubility

Solubilisation Soluble

Solubilisation and its Effect on Transport

Solubilisation and microemulsion

Solubilisation of triglycerides

Solubilisation theories

Solubilisation, assisted

Solubilised Chemicals Which Cause Antifoaming

Solubilised Chemicals that Cause Antifoaming

Solubilised enzymes

Solubilised systems

Solubilised vat dyes

Solubiliser

Solubiliser

Steroids solubilisation

Surfactants solubilisation

Vitamin polysorbate solubilisation

Water solubilising groups

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