Acidic samples

Abstract. A model of the conformational transitions of the nucleic acid molecule during the water adsorption-desorption cycle is proposed. The nucleic acid-water system is considered as an open system. The model describes the transitions between three main conformations of wet nucleic acid samples A-, B- and unordered forms. The analysis of kinetic equations shows the non-trivial bifurcation behaviour of the system which leads to the multistability. This fact allows one to explain the hysteresis phenomena observed experimentally in the nucleic acid-water system. The problem of self-organization in the nucleic acid-water system is of great importance for revealing physical mechanisms of the functioning of nucleic acids and for many specific practical fields. 

Lahajnar, G., Zupancic, L, Rupprecht, A. Proton NMR relaxation and diffusion study of water sorbed in oriented DNA and hyaluronic acid samples. In Biophysics of Water (Franks, F., Mathias, S., eds) Wiley, New York (1982) 231-234... 

Saure-lostmg,/. solution of an acid, -maschine, /. souring machine, -menge, /. amount of acid, -messer, m. acidimeter hydrometer, -messkunst, /. acidimetry. -messtmg, /. acidimetry. -probe, /. acid test acid sample, -pumpe,/. acid pump, -radikal, n. acid radical, -regenerat, n. Rubber) acid reclaim. 

Fluoride ion, and weak acids and bases do not interfere, but nitrate, nitrite, perchlorate, thiocyanate, chromate, chlorate, iodide, and bromide do. Since analysis of almost all boron-containing compounds requires a preliminary treatment which ultimately results in an aqueous boric acid sample, this procedure may be regarded as a gravimetric determination of boron. 

Dissolve a known weight (ca 0.5 g) of the steel by any suitable procedure. Treat the acidic sample solution (< 200 /jg Co), containing iron in the iron(II) state, with 10-15 mL of 40 per cent (w/v) sodium citrate solution, dilute to 50-75 mL and adjust the pH to 3-4 (indicator paper) with 2M hydrochloric acid or sodium hydroxide. Cool to room temperature, add 10 mL of 3 per cent (10-volume) hydrogen peroxide and, after 3 minutes, 2mL of the reagent solution. Allow to stand for at least 30 minutes at room temperature. Extract the solution in a separatory funnel by shaking vigorously for 1 minute with 25 mL of chloroform repeat the extraction twice with 10 mL portions of chloroform. Dilute the combined extracts to 50 mL with chloroform and transfer to a clean separatory funnel. Add 20 mL of 2M hydrochloric acid, shake for 1 minute, run the chloroform layer into another separatory funnel, and shake for 1 minute with 20 mL of 2M sodium hydroxide. Determine the absorbance of the clear chloroform phase in a 1 cm cell at 530 nm. 

The source materials were commercial pectins apple A30 and citrus pectin C73 kindly supplied by Unipectine (France) and Copenhagen Pectin Factory (Denmark) respectively. Polygalacturonic acid samples (named SR) were obtained by acid hydrolysis of a fully de-esterified citrus pectin as previously described [24]. Citrus pectins with different degree of esterification (DE) were obtained by controlled acid de-esterification [8]. 

The Fourier Trairsform Infrared (FTIR) spectrum obtained from non-adapted tomato cell walls is very similar to that from the onion parenchyma cell wall (both contain cellulose, xyloglucan and pectin) although there is more protein in the tomato walls (amide stretches at 1550 and 1650 cm-i) (Fig 4). In DCB-adapted tomato cell walls, the spectrum more closely resembles that of either purified pectins or of a commercial polygalacturonic acid sample from Sigma with peaks in common at 1140, 1095, 1070, 1015 and 950 cm-t in the carbohydrate region of the spectrum as well as the free acid stretches at 1600 and 1414 cm-i and an ester peak at 1725 cm-k An ester band at 1740 cm-i is evident in both onion parenchyma and non-adapted tomato cell wall samples. It is possible that this shift in the ester peak simply reflects the different local molecular environment of this bond, but it is also possible that a different ester is made in the DCB-adapted cell walls, as phenolic esters absorb around 1720 cm-i whilst carboxylic esters absorb at 1740 cm-k The... 

This assay system developed by Chaires [136] is a new, powerful and effective tool based on the fundamental thermodynamic principle of equilibrium dialysis for the discovery of ligands that bind to nucleic acids with structural and sequence selectivity. Here, identical concentrations of various nucleic acid samples are dialysed in dispodialysers against a common ligand solution. At equilibrium, the contents of the ligand bound to each nucleic acid are determined and this is correlated directly to the ligand s specificity to a particular sequence. 

FIGURE 2.6 Concentration profiles of (a) hexadecanoic acid, sample concentration C = 0.025 mol 1 , (b) dodecanoic acid, sample concentration C = 0.1 mol 1" , obtained on microcrystalline cellulose with decaline as mobile phase [20]. 

Figure 9 Three-dimensional cationic CITP of (A) blank (B) lysozyme (LYSO), creatinine (CREAT), conalbumin (CAL), y-amino-n-butyric acid (GABA), and ovalbumin (OVA) (C) OVA spiked with CREAT and GABA. Capillary 90 cm (length to the detector, 70 cm) x 75 p i.d. leader 10 mM potassium acetate and acetic acid with 0.3% HPMC, pH 4.75 terminator 10 mM acetic acid sample 10 to 30 mg/ml proteins dissolved in leader without HPMC voltage 20 kV. (From Gebauer, P. and Thormann, W.,. Chromatogr., 558, 423, 1991. With permission.)...

Fig. 22 Dissolution fates of various griseofulvin and gri-seofulvin-succinic acid samples as determined by the oscillating bottle method. , griseofulvin, crystalline A, griseofulvin, micronized , eutectic mixture 0> physical mixture at eutectic composition , solid solution A, physical mixture at solid solution composition. The dashed line indicates the equilibrium solubility of griseofulvin in water. (From Ref. 41.).

To a 500 g sample of acidic, dealuminized mordenite (CBV-20A from PQ Corporation, 1.5 mm diameter extrudates that had been calcined at 540 °C, overnight) was added a solution of 33 ml of 48% HF in 1633 ml of distilled water, and the mix cooled in ice, stirred on a rotary evaporator overnight, then filtered to recover the extruded solids. The extrudates were further washed with distilled water, dried in vacuo at 100 °C, and then calcined at 540 °C, overnight. Analyses of the treated mordenite showed 1.2% fluoride, 0.49 meq/g acidity. Samples were charged to the reactive distillation unit either as 20/40 mesh granules, or as ca. 1.5 mm extrudates. 

Armstrong, D.W., Duncan, J.D., Lee, S.H. (1991). Evaluation of d-Amino acid levels in human urine and in commercial L-amino acid samples. Amino Acids 1, 97-106. 

Log k appears to correlate with log P for standards between log P —0.5 to 5.0. One limitation of this method is that solutes must be electrically neutral at the pH of the buffer solution because electrophoretic mobility of the charged solute leads to migration times outside the range of Tm and TEof- Basic samples are therefore run at pH 10, and acidic samples at pH 3, thus ensuring that most weak acids and bases will be in their neutral form. This method has been used in a preclinical discovery environment with a throughput of 100 samples per week [24]. 

This conclusion is based on a high char yield and similar rates of mass loss at 300°C for untreated and boric acid treated samples. Boric acid samples also had much higher AH+ s and, consequently, higher Ea s. Our results suggest that certain thermally-stable, weak polybasic acids which can complex with polysaccharides may provide fire-resistant properties to lignocellulosics. The results and conclusions were strongly influenced by the technique used to analyze the TGA data. 

The mass loss rates for the boric acid samples were comparable to the untreated samples, despite a higher char yield (Table IX) for the treated samples. This was unexpected since the role of a wood fire retardant is to increase the char by increasing the dehydration reaction (1,3,7). Thus, a fire retardant treated sample will actually pyrolyze at a lower temperature. Data from Table III suggests that boric acid may form more char by suppressing formation of flammable volatiles instead of by increasing the dehydration rate. 

It is usually convenient to identify the angles of the 10 most intense scattering peaks in a powder pattern, and to then list the accepted tolerance ranges of these based on the diffractometer used for the determinations. Such a representation has been developed for data obtained for racemic mandelic acid, and for its separated (S)-enantiomer, using a diffractometer system whose precision was known to be +0.15 degrees 26 [30]. The criteria are shown in Table 7.9, the form of which enables the ready identification of a mandelic acid sample as being either racemic or enantiomerically pure. It should be noted that the powder pattern of the separated (i )-enantiomer would necessarily have to be identical to that of the separated (S)-enantiomer. 

The reactions were carried out in each case with a 0-1 per cent protein solution in phosphate buffer (pH 6 8), to which the radioactive phosphorofluoridate was added as a concentrated solution in dry ethanol. At the end of the reaction time, the product was dialysed for 20 hr. against running water, and precipitated at 0° by addition of two volumes of acetone. The precipitate was spun off and washed at —5° with ethanol and ether, and dried in air or over sulphuric acid. Samples of 25-50 mg. of dry powder were used for radioactivity determinations, and compared with a standard prepared by hydrolysing a weighed amount (ca. 1 mg.) of the phosphorofluoridate in n sodium hydroxide, neutralizing and drying. 

The energy of combustion of benzoic acid determined by standardizing laboratories normally refers to the following certification conditions [21,25,39-43] (1) The benzoic acid sample is burned in a bomb at constant volume, in pure oxygen at an initial pressure of 3.04 MPa (2) the mass of sample burned, expressed in grams, is equal to three times the internal volume of the bomb in dm3 (3) the amount of water inside the bomb, expressed in grams, is also equal to three times the internal volume of the bomb in dm3 (4) the combustion reaction is referred to 298.15 K. If calibrations are not made strictly under the certification conditions, the value of Acm(BA) under the actual bomb conditions should... 

In equations 7.27 and 7.28 m(BA), m(cot), m(crbl), and m(wr) are the masses of benzoic acid sample, cotton thread fuse, platinum crucible, and platinum fuse wire initially placed inside the bomb, respectively n(02) is the amount of substance of oxygen inside the bomb n(C02) is the amount of substance of carbon dioxide formed in the reaction Am(H20) is the difference between the mass of water initially present inside the calorimeter proper and that of the standard initial calorimetric system and cy (BA), cy(Pt),cy (cot), Cy(02), and Cy(C02)are the heat capacities at constant volume of benzoic acid, platinum, cotton, oxygen, and carbon dioxide, respectively. The terms e (H20) and f(sin) represent the effective heat capacities of the two-phase systems present inside the bomb in the initial state (liquid water+water vapor) and in the final state (final bomb solution + water vapor), respectively. In the case of the combustion of compounds containing the elements C, H, O, and N, at 298.15 K, these terms are given by [44]... 

Some concentrated nitric acid may be produced as a by-product in the SILVER II process when processing energetics compounds, which contain nitrogen. The material will be collected and sold to off-site users. During Demo II testing, analysis of nitric acid samples by the Ensign-Bickford Company determined that the... 

Potable water and raw source water Sample acetylated in situ by addition of acetic anhydride, solvent extracted and concentrated alternatively, extracted acidic sample derivatized by pentafluorobenzyl bromide and cleaned up by column chromatography HRGC-ECD (for pentafluorobenzyl derivative) HRGC-MS (for acetyl derivative) <50 ng/L (pentafluorobenzyl) <50 ng/L (acetyl derivative) 10-64% (pentafluorobenzyl derivative) 70-132% (acetyl derivative) Sitholeetal. 1986... 

The complex chemistry of Se provides many options for purihcation, but also causes some difficulties in sample preparation. Notably, evaporation of an HCl matrix to dryness causes severe loss of Se (Chau and Riley 1965). Storage of Se(lV) samples for long periods can lead to losses due to reduction to Se(0). Standard ion exchange methods are not effective with acidic sample matrices, as Se(lV) is present as uncharged H2Se03 at pH < 2 (Fig. 1). 

The enantioselectivity factors in Table 10 indicate that amino acid samples with different enantiomeric excess (ee) should show differences in the R = (1 + I5)/Iref term. Indeed, In Rchkai is linearly related to optical purity of the specimen and the relevant calibration curve can be established. Accordingly, it is possible to rapidly determine ee of an amino acid sample by a single measurement of Rchirai in a tandem... 

Figure 10.17 H NMR spectra of spent acid samples spanning operational range of sulfuric acid concentrations. Shift of sulfuric acid peak with change in acid strength is indicated. Acid soluble oils and micellar water are readily quantified.

The thermal depolymerization of polyoxymethylene starts from the unstable hydroxy end groups, but the oxidative and acid-catalyzed hydrolytic degradation takes place within the main chain. Flence, if polyoxymethylene is heated in air or in the presence of strong acids samples with blocked end groups will also degrade. 

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