Pestle and mortar

Crushing and grinding uses mechanical force to break larger particles into smaller ones. A variety of tools are used depending on the particle s size and hardness. Large particles are crushed using jaw crushers capable of reducing particles to diameters of a few millimeters. Ball mills, disk mills, and mortars and pestles are used to further reduce particle size. 

Because of the risk of lead poisoning, the exposure of children to lead-based paint is a significant public health concern. The first step in the quantitative analysis of lead in dried paint chips is to dissolve the sample. Corl evaluated several dissolution techniques. " In this study, samples of paint were collected and pulverized with a Pyrex mortar and pestle. Replicate portions of the powdered paint were then taken for analysis. Results for an unknown paint sample and for a standard reference material, in which dissolution was accomplished by a 4-6-h digestion with HNO3 on a hot plate, are shown in the following table. 

Samples of animal bones weighing approximately 3 g are ashed at 600 °C until the entire bone is ash-white. Samples are then crushed in a mortar and pestle. A portion of the sample is digested in HCl and diluted to a known volume. The concentrations of zinc and strontium are determined by atomic absorption. The analysis for strontium illustrates the use of a protecting agent as La(N03)3 is added to prevent an interference due to the formation of refractory strontium phosphate. 

Several aspirin tablets are ground to a fine powder in a mortar and pestle. A 0.1013-g portion of the powder is placed in a 1-L volumetric flask and diluted to volume with distilled water. A portion of this solution is filtered to remove insoluble binders, and a 10.00-mL aliquot transferred to a 100-mL volumetric flask containing 2.00 ml of 4 M NaOH. After diluting to volume the fluorescence of the resulting solution is found to be 8.69. What is the %w/w acetylsalicylic acid in the aspirin tablets ... 

A MIXTURE of 120 g. (3 moles) of sodamide (Note i) and 200 cc. of purified mineral oil (Note 2) is ground together in a mortar until the amide is finely pulverized (Note 3). This suspension is transferred to a 2-I. round-bottom, three-necked flask fitted with a reflux condenser holding a calcium chloride tube, a 500-cc. separatory funnel, and an efficient mechanical stirrer through a mercury seal. The mortar and pestle are rinsed with an additional 250 cc. of the oil which is then added to the reaction flask. This is heated in an oil bath maintained at 160-165, the stirrer is started and 203 g. (i mole) of cyclohexylbromopropene (p. 20) is dropped in during one and one-half hours. Ammonia is evolved and this is allowed to pass through the condenser and is collected in water. 

This must be ground into a fine powder with a mortar and pestle immediately prior to use. 

The absence of water in the lithium bromide is of great importance. Traces of wrater lower the yield of product by 10-20%. LiBr-2 H20 (purchased from E. Merck Company, Inc., Darmstadt or City Chemical Corporation) was dissolved three times in anhydrous acetonitrile-benzene (1 1), and the solvents removed each time on a rotary evaporator. The lithium bromide was dried under high vacuum at 100° for 1 hour, ground to a fine powder with a mortar and pestle while still warm, and again dried at 100°, as above, for 3 hours. 

On the other hand, quantitative extraction requires complete and exhaustive extraction and no material can be lost. To assure complete extraction when a food is analyzed for the first time in a laboratory, it is useful to carry out two or three extractions, pool the solvents, and keep separate the next extracts to verify the presence of carotenoids. Usually four to six extractions are enough to remove the carotenoids completely from a sample. The extraction can be carried out in a blender, vortex, or with a mortar and pestle. Accelerated solvent extraction (ASE), an important extraction technique in residue analysis, currently attracts interest due to its short duration, low level of solvent use, and high extraction yield. The average recoveries for all carotenoids with the exception of norbixin ranged from 88.7 to 103.3% using manual extraction and from 91.0 to 99.6% by ASE (70 bar and temperature of 40°C) both extractions were carried out with a mixture of MeOH, EtOAc, and petroleum ether (1 1 1). ... 

Determination of Metal Precursor Mobilities During Pretreatment. Relative precursor mobilities were obtained by premixing the sllica-or alumina-supported metal catalysts with pure silica (Cab-O-Sll, grade M-5, Cabot Corp.) or pure alumina (Alon C, Cabot Corp.) In a 1 2 ratio prior to pretreatment. The catalyst and silica were ground together using a mortar and pestle for at least 0.5 hr. before they were placed in the Pyrex microreactor for pretreatment. 

The primary consideration for all AEM analysis is that the specimen be thin (generally carbon coated electron microscope grid either dry or in a suitable liquid. If a liquid suspension is used in preparing the specimen, it is important that all elements of interest are insoluble in that liquid. Only particles thin enough to meet AEM thin-film criteria (15) should be analyzed quantitatively. Scraping surface particles from a catalyst pellet for specimen preparation may be more useful than grinding the entire pellet. 

Pd on Carbon. The catalyst analyzed here is a commercial hydrogenation catalyst with 5% Pd supported on activated carbon (Alfa). The catalyst was ground in a mortar and pestle and dispersed dry onto a carbon coated Cu grid. While x-ray spectra from heavy metal particles down to 2nm in diameter can be obtained (O by manually directing the electron beam to the particle, digital images of Pd particles at high resolution have not been obtained previously. 

Beef kidney samples were analyzed for atrazine by dispersing 0.5-g portions of kidney with 2-g portions of XAD-7 HP resin for matrix solid-phase dispersion. " By using a mortar and pestle, a powder-like mixture was prepared that was subjected to subcritical extraction using ethanol-modified water at 100 °C and 50 atm. The ethanol-water extract was sampled using a CW-DVB SPME fiber for direct analysis using ion-trap GC/MS, and the recoveries were quantitative for atrazine at the 0.2 mg kg fortification level. 

Use a mortar and pestle to grind a piece of tablet into a powder. Repeat steps 2 through 5, using the powdered tablet. 

Irradiation of (+ )-crystals of 96 with a 400 W high-pressure Hg-lamp, with occasional grinding with an agate mortar and pestle for 40 h at room temperature gave ( + )-97 of 93 % ee in 74 % yield. Irradiation of (—)-crystals of 96 under the same conditions gave (—)-97 of 93 % ec in 75% yield48. Purification to 100% ee can easily be achieved by recrystallization from benzene. Although the photochemical conversion of 96 into 97 on irradiation in the solid state has been reported, enantioselectivity of the reaction has not been discussed 441. 

The hydride can be pulverized rapidly and safely by breaking the large pieces with a spatula, followed by careful crushing with a mortar and pestle. Caution must be observed because the solid may inflame on prolonged grinding or abrasion. The hydride dust is caustic and irritating. 

Lyse by mechanical grinding using a porcelain mortar and pestle. Add further LN2 as necessary during the grinding, until a fine, whitish powder is formed. The LN2 must not be allowed to evaporate completely or the cells will start to thaw and form an unmanageable paste. 

Unde type 4A molecular sieve pellets were crushed using a mortar and pestle and then dried under vacuum (0.3 mm) at 300°CS for 15 hr prior to use. 

Potassium phosphate was obtained from Mallinckrodt Chemical and was dried at >500°C for > 12 hr, cooled in a desiccator, ground to a fine powder with a mortar and pestle, and stored in a desiccator before use. It must be weighed quickly, as it is hygroscopic. 

Char Preparatioa Chars were prepared both by isothermal pyrolysis of 5 g samples of resin in a quartz boat heated in an atmosphere of flowing (0.5 SCFM) N2 in a quartz tube oven (N2 pyrolysis chars) and by open combustion of 1 g samples of resin exposed to 2.8 watts/cm2 of radiant energy from an electric heating panel (4-5) (combustion or burn chars). All chars were finely ground with a glass mortar and pestle prior to analysis. 

For NMR spectroscopic experiments, a thin film of pTrMPTrA was prepared by reacting a quantity of monomer and photoinitiator confined between glass plates with 1 mm separation. The polymerization conditions were the same as those for the photocalorimetry experiments. After 1 hour of UV exposure, the film was removed from the plates and ground to a fine powder using a mortar and pestle. A solid-state 13C NMR spectrum of the powder was obtained immediately, as described below. The remaining polymer powder was divided into two portions, one of which was stored under atmospheric conditions. The other portion was stored under N2. After one week, 13c spectra were again obtained for each of these polymer samples. Both samples were then heated to 280 °C in a vacuum oven and analyzed once more by 13C NMR spectroscopy. 

Frozen in liquid nitrogen, ground into powder in chilled mortar and pestle extracted with 10 mL HC1/KC1 buffer, centrifuged at 12,000 X g... 

Clean the plates with anhydrous acetone or ethanol. NOT WATER If you don t have the tiny agate mortar and pestle, try a Witt spot plate and the rounded end of a thick glass rod. The spot plate is a piece of glazed porcelain with dimples in it. Use one as a tiny mortar the other as a tiny pestle. 

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