Aqueous aging

Hamster, 241 Am nitrate, aqueous % Age Absorption estimate based on comparisons with David and Harrison... 

Albertsson A-C (1977) Studies on mineralization of14C labelled polyethylenes in aerobic biodegradation and aqueous aging. PhD Thesis, Royal Institute of Technology, Stockholm, Sweden... 

Haqu, M. et al.. Influence of aqueous aging on surface properties of plasma sprayed oxide coatings, J. Colloid Interf. Sci., 313, 194, 2007. 

Mazzucco DC, Dumbleton J, Kurtz SM. Can accelerated aqueous aging simulate in vivo oxidation of gamma-sterilized UHMWPE J Biomed Mater Res B Appl Biomater 2006 October 79(l) 79-85. 

S. M. Kurtz, R. L. Siskey, and J. Dumbleton. Accelerated aqueous aging simulation of in vivo oxidation for gamma-sterilized UHMWPE. Journal of Biomedical Materials Research - Part B Applied Biomaterials 90 (1), 368-372... 

An example of the time effects in irreversible adsorption of a surfactant system is shown in Fig. XI-8 for barium dinonylnapthalene sulfonate (an oil additive) adsorbing on Ti02 (anatase). Adsorption was ineversible for aged systems, but much less so for those equilibrating for a short time. The adsorption of aqueous methylene blue (note Section XI-4) on TiOi (anatase) was also irreversible [128]. In these situations it seems necessary to postulate at least a two-stage sequence, such as... 

Niobic Acid. Niobic acid, Nb20 XH2O, includes all hydrated forms of niobium pentoxide, where the degree of hydration depends on the method of preparation, age, etc. It is a white insoluble precipitate formed by acid hydrolysis of niobates that are prepared by alkaH pyrosulfate, carbonate, or hydroxide fusion base hydrolysis of niobium fluoride solutions or aqueous hydrolysis of chlorides or bromides. When it is formed in the presence of tannin, a volurninous red complex forms. Freshly precipitated niobic acid usually is coUoidal and is peptized by water washing, thus it is difficult to free from traces of electrolyte. Its properties vary with age and reactivity is noticeably diminished on standing for even a few days. It is soluble in concentrated hydrochloric and sulfuric acids but is reprecipitated on dilution and boiling and can be complexed when it is freshly made with oxaHc or tartaric acid. It is soluble in hydrofluoric acid of any concentration. 

Physical and chemical properties of the numerous PAG products can vary considerably. PAG products are usually aqueous solutions, although soHd products are also sold. Solutions range from colodess to amber and from clear to hazy in appearance specific gravities at 25 °G vary from about 1.2 to 1.35. Product viscosities, as measured by a Brookfield viscometer at 25 °G, are generally about 10 50 mPa-s(=cP), but can be much greater than 10, 000 mPa-s(=cP) for certain aged compositions. 

Preparation of Pillared Clay Catalysts. PAG products are used for the preparation of zeolite-like catalysts by intercalation, the insertion of Al polycations molecules between the alurninosiHcate sheets of clay (3,33). Aqueous clay suspensions are slowly added to vigorously stirred PAG solutions, and the reaction mixture is aged for several hours. The clay is separated from the PAG solution and washed free of chloride ion. The treated clay is first dried at low temperature and then calcined in air at 450—500°G, producing a high surface area material having a regular-sized pore opening of about 0.6 to... 

Rosin ester resins are used extensively in pressure-sensitive adhesives as tackifiers. The adhesive is formulated by blending the resin with a polymer in solution or as aqueous emulsions. Typical compositions may contain about 50% resin. The glycerol or pentaerythritol esters of stabilized rosins are often used because they are stable on aging. 

Riboflavin is widely used in the pharmaceutical, food-enrichment, and feed-supplement industries. Riboflavin USP is adininistered orally in tablets or by injection as an aqueous solution, which may contain nicotinamide or other solubilizers. As a supplement to animal feeds, riboflavin is usually added at concentrations of 2—8 mg/kg, depending on the species and age of the animal (see Feeds AND FEED ADDITIVES). 

The hydrolysis of (eq. 4) and the addition of less than equivalent amounts of hydroxide ion to aqueous solutions of, followed by aging,... 

Cr2 03 - 112 0, of indefinite composition occurs. This compound is commonly misnamed as chromic or chromium (ITT) hydroxide [1308-14-1], Cr(OH)2. A tme hydroxide, chromium (ITT) hydroxide trihydrate [41646-40-6], Cr(OH)2 3H20, does exist and is prepared by the slow addition of alkaU hydroxide to a cold aqueous solution of hexaaquachromium(III) ion (40). The fresh precipitate is amphoteric and dissolves in acid or in excess of hydroxide to form the metastable Cr(OH). This ion decomposes upon heating to give the hydrous chromium (ITT) oxide. However, if the precipitate is allowed to age, it resists dissolution in excess hydroxide. 

The spectacular success (in 1807) of Humphry Davy, then aged 29 y, in isolating metallic potassium by electrolysis of molten caustic potash (KOH) is too well known to need repeating in detail." Globules of molten sodium were similarly prepared by him a few days later from molten caustic soda. Earlier experiments with aqueous solutions had been unsuccessful because of the great reactivity of these new elements. The names chosen by Davy reflect the sources of the elements. 

In203 has the C-type M2O3 structure (p. 1238) and InO(OH) (prepared hydrothermal ly from In(OH)3 at 250-400°C and 100-1500 atm) has a deformed rutile structure (p. 961) rather than the layer lattice structure of AIO(OH) and GaO(OH). Crystalline In(OH)3 is best prepared by addition of NH3 to aqueous InCl3 at 100° and ageing the precipitate for a few hours at this temperature it has the simple Re03-type structure distorted somewhat by multiple H bonds. 

The reactor is loaded with a solution of emulsifier in an organic solvent and the aqueous monomer solution (20-60%) is dispersed in the organic phase by stirring. The obtained emulsion is deoxygenated by purging dry nitrogen or by multiple evacuation and thermostated at 30-60°C. Then, an initiator solution is introduced in the reaction mixture and the process is carried out at 30-60°C for 3-6 h, after which the reaction mixture is aged for 1-5 h. 

Potentiometric titrations - continued EDTA titrations, 586 neutralisation reactions, 578, 580 non-aqueous titrations, 589, (T) 590 oxidation-reduction reactions, 579, 581, 584 precipitation reactions, 579, 582 Potentiometry 548 direct, 548, 567 fluoride, D. of, 570 Potentiostats 510, 607 Precipitants organic, 437 Precipitate ageing of, 423 digestion of, 423... 

The reflux of aqueous Pu(IV) solutions containing <6 M HNO3 produces polymer precipitates that are resistant to subsequent dissociation and dissolution in nitric acid. Eapid aging of the Pu(IV) polymer to form a PuC -like structure is responsible for the unusually stable polymer. Comparative studies under nonreflux conditions show that polymer does not form at concentrations of HNO3 >3 M. 

Plutonium(IV) polymer is a product of Pu(IV) hydrolysis and is formed in aqueous solutions at low acid concentrations. Depolymerization generally is accomplished by acid reaction to form ionic Pu(IV), but acid degradation of polymer is strongly dependent on the age of the polymer and the conditions under which the polymer was formed (12). Photoenhancement of Pu(IV) depolymerization was first observed with a freshly prepared polymer material in 0.5 HClOh, Fig. 3 (3 ). Depolymerization proceeded in dark conditions until after 140 h, 18% of the polymer remained. Four rather mild 1-h illuminations of identical samples at 5, 25, 52, and 76 h enhanced the depolymerization rates so that only 1% polymer remained after the fourth light exposure (Fig. 3). 

In studies on Pt dotted silicon electrodes, PMC measurements revealed that tiny Pt dots increased the interfacial charge transfer compared with bare silicon surfaces in contact with aqueous electrolytes. However, during an aging effect, the thickness of the oxide layer between the silicon and the platinum dots gradually increased so that the kinetic advantage again decreased with time.11... 

The synthetic approach is very simple and does not require any special set up. In a typical room temperature reaction, 1.0 mL aqueous solution of cadmium chloride was added to 20 mL aqueous solution of soluble starch in a 50 mL one-necked round-bottom flask with constant stirring at room temperature. The pH of the solution was adjusted from 6 to 11 using 0.1 M ammonia solution. This was followed by a slow addition of 1.0 mL colourless selenide ion stock solution. The mixture was further stirred for 2 h and aged for 18 h. The resultant solution was filtered and extracted with acetone to obtain a red precipitate of CdSe nanoaprticles. The precipitate was washed several times and dried at room temperature to give a material which readily dispersed in water. The same procedure was repeated for the synthesis of PVA and PVP - capped CdSe nanoparticles by replacing the starch solution with the PVA and PVP polymers while the synthesis of elongated nanoparticles was achieved by changing the Cd Se precursor ratio from 1 1 to 1 2. The synthesis of polymer capped ZnSe nanoparticles also follows the same procedure except that ZnCb solution was used instead of CdCb solution. 

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