Paper soluble

Nuss, /. nut specif., walnut, -baum, m. nut tree, specif, walnut, -beize, /. (Paper) soluble brown. 

The combination with GPC is limited to pulps and papers soluble in DMAc/LiCl. 

In this paper solubility measurements of synthetic and natural dyestuffs are presented using VIS-spectroscopy. The investigations concentrate on two different methods. I. P-carotene was measured as a function of temperature and pressure in near- and supercritical C02 (289 to 309 K, 10 to 160 MPa) and CC1F3 (297 to 326 K, 12 to 180 MPa), respectively, using a static method. II. Additionally, the solubilities of l,4-bis-(n-alkylamino)-9,10-anthraquinones (with n-alkyl = butyl, octyl) were determined with a dynamic method in temperature and pressure ranges from 310 to 340 K and 8 to 20 MPa, respectively this method permits a continuous purification from better soluble impurities as well as the measurement of solubilities at the same time. For both anthraquinone dyestuffs intersection points of the solubility isotherms were found in the plot of concentration versus pressure. This behavior can be explained by a density effect. 

Properties White, crystalline powder odorless darkens slowly on exposure to light. Mp 166-170C. Solutions practically neutral to litmus paper soluble in water, alcohol, and chloroform very slightly soluble in benzene and ether. 

Properties A blue, amorphous powder frequently compressed into small cakes or strips ( paper ). Soluble in water changes color with acidity of solution, red at pH 4.5, blue at pH 8.3. 

J. 1837-1838. Nitrated paper, soluble in ethyl alcohol, and nitrated cotton fibers, insoluble in ethyl alcohol, were prepared by Prof. Theophile Jules Pelouze, a French chemist. These products were highly combustible. 

Other uses - The hemihydrate form is used in a wide variety of construction and industrial plasters. Minor amoimts of purified gypsum are used in glassmaking and as a white filler (terra alba) in paint and paper. Soluble anhydrite , made by dehydrating gypsum into porous, highly absorbent granules, is used as a desiccant. 

The blackening of filter paper, moistened with a soluble lead(II) salt (e.g. the ethanoate or nitrate), by the formation of lead(II) sulphide. 

Paper chromatography in particular frequently enables the components of a mixture to be separated and identified when only 1-2 mg. of the mixture are available, the process being independent of the relative solubilities of the components. 

The oxime is freely soluble in water and in most organic liquids. Recrystallise the crude dry product from a minimum of 60-80 petrol or (less suitably) cyclohexane for this purpose first determine approximately, by means of a small-scale test-tube experiment, the minimum proportion of the hot solvent required to dissolve the oxime from about 0-5 g. of the crude material. Then place the bulk of the crude product in a small (100 ml.) round-bottomed or conical flask fitted with a reflux water-condenser, add the required amount of the solvent and boil the mixture on a water-bath. Then turn out the gas, and quickly filter the hot mixture through a fluted filter-paper into a conical flask the sodium chloride remains on the filter, whilst the filtrate on cooling in ice-water deposits the acetoxime as colourless crystals. These, when filtered anddried (either by pressing between drying-paper or by placing in an atmospheric desiccator) have m.p. 60 . Acetoxime sublimes rather readily when exposed to the air, and rapidly when warmed or when placed in a vacuum. Hence the necessity for an atmospheric desiccator for drying purposes. 

The recrystallisation of diazoaminobenzene has to be performed with care, as the substance is freely soluble in most liquids and tends moreover to decompose if its solution is not rapidly cooled. Place 2 g. of the crude, freshly prepared, well-drained material in a boiling-tube, add about 15-20 ml. of ethanol and 1-2 drops of 10% aqueous sodium hydroxide solution, and then heat rapidly until boiling if the solution should contain insoluble impurities, filter through a small fluted paper, and at once cool the filtrate in ice-water. The diazoaminobenzene should rapidly crystallise out from the cold and stirred solution filter the crystals rapidly at the pump whilst the solution is still cold, as... 

Solubility in water and action of solution on litmus-paper. 

Dissolve 36 g. of p-toluidine in 85 ml. of concentrated hydrochloric acid and 85 ml. of water contained in a 750 ml. conical flask or beaker. Cool the mixture to 0° in an ice-salt bath with vigorous stirring or shaking and the addition of a httle crushed ice. The salt, p-toluidine hydrochloride, will separate as a finely-divided crystalline precipitate. Add during 10-15 minutes a solution of 24 g. of sodium nitrite in 50 ml. of water (1) shake or stir the solution well during the diazotisation, and keep the mixture at a temperature of 0-5° by the addition of a httle crushed ice from time to time. The hydrochloride wUl dissolve as the very soluble diazonium salt is formed when ah the nitrite solution has been introduced, the solution should contain a trace of free nitrous acid. Test with potassium iodide - starch paper (see Section IV,60). 

Dissolve 5 g. of finely-powdered diazoaminobenzene (Section IV,81) in 12-15 g. of aniline in a small flask and add 2-5 g. of finely-powdered aniline hydrochloride (1). Warm the mixture, with frequent shaking, on a water bath at 40-45° for 1 hour. Allow the reaction mixture to stand for 30 minutes. Then add 15 ml. of glacial acetic acid diluted with an equal volume of water stir or shake the mixture in order to remove the excess of anihne in the form of its soluble acetate. Allow the mixture to stand, with frequent shaking, for 15 minutes filter the amino-azobenzene at the pump, wash with a little water, and dry upon filter paper Recrystallise the crude p-amino-azobenzene (3-5 g. m.p. 120°) from 15-20 ml. of carbon tetrachloride to obtain the pure compound, m.p. 125°. Alternatively, the compound may be recrystaUised from dilute alcohol, to which a few drops of concentrated ammonia solution have been added. 

Solubility in water. Treat a 0 10 g. portion of the solid with successive 10 ml. portions of water, shaking vigorously after each addition, until 3 0 ml. have been added. If the compound does not dissolve completely in 3 0 ml. of water, it may be regarded as insoluble in water. When dealing with a liquid, add 0 -20 ml. of the compound to 3 0 ml. of water and shake. In either case, test the contents of the small test-tube with htmus (or with Universal indicator paper) it is best to remove a little of the solution or supernatant liquid with a dropper. 

Reaction with Chlorine. Polyacrylamide reacts with chlorine under acid conditions to form reasonably stable A/-chloroamides. The polymers are water soluble and can provide good wet strength and wet web strength in paper (60). 

Eyrol 51 is a water-soluble Hquid containing about 21% phosphoms. It is made by a multistep process from dimethyl methylphosphonate, phosphoms pentoxide, and ethylene oxide. The end groups are principally primary hydroxyl and the compound can thus be incorporated chemically into aminoplasts, phenoHc resins, and polyurethanes. Eyrol 51, or 58 if diluted with a small amount of isopropanol, is used along with amino resins to produce a flame-retardant resin finish on paper used for automotive air filters, or for backcoating of upholstery fabric to pass the British or California flammabiHty standards. 

Margarine and butter contain fat plus water and water-soluble ingredients, eg, salt and milk soHds that impart flavor and color to the product. Generally these products are distributed at refrigerated temperatures to retain their quaHty. Greaseproof packaging, such as polyethylene-coated paperboard, aluminum foil/paper, parchment paper wraps, and polypropylene tubs, is used for butter and margarine (see Dairy substitutes). 

Tripotassium hexakiscyanoferrate [13746-66-2] K2[Fe(CN)g], forms anhydrous red crystals. The crystalline material is dimorphic both orthorhombic and monoclinic forms are known. The compound is obtained by chemical or electrolytic oxidation of hexacyanoferrate(4—). K2[Fe(CN)g] is soluble in water and acetone, but insoluble in alcohol. It is used in the manufacture of pigments, photographic papers, leather (qv), and textiles and is used as a catalyst in oxidation and polymerisation reactions. 

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