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Modifier acidic

These results contrasted sharply with those obtained with a HHT that was relatively unstable to the reaction conditions. For example, the commercially available HHT of glycinonitrile 28 gave a very poor yield (6%) of coupled glyphosate product with diethyl phosphite because the reaction must be run with acid-catalysis at much lower temperatures (27,38). Somewhat higher yields were observed when 28 was used directly under the modified, acidic Mannich conditions to provide iV-phosphonomethylglycinonitrile 29, which was hydrolyzed direedy to GLYNa3 (39). [Pg.23]

No Pressure, bar Modifier Acid added, M Rate contant min Conv. % Optical yield. [Pg.247]

Simplest method of diagnosis is detection of oocysts by modified acid-fast staining of a stool specimen. Standard ova and parasite test does not include Cryptosporidium. [Pg.1124]

Acid-fast staining for Cryptosporidium sp. has recently become important because this parasite is now recognized as a cause of severe diarrhea in immunodeficient patients such as those with AIDS, and it can cause transient diarrhea in immunocompetent individuals. The modified acid-fast stain recommended is similar to that used to stain Nocardia spp. in that it uses milder acid decolorization. A variety of acid-fast and fluorochrome staining procedures have been described for Cryptosporidium spp., and all the procedures appear to work. [Pg.20]

The properties of PCTA-type structures where the modifying acid is 1,4-cyclohexanedicarboxylic acid (CHDA) have also been studied [53], The incorporation of this diacid (95 % trans) as a polyester modifier maintains the toughness, but is accompanied with significant lowering of the Tg. This is contrasted to NDA modification where the Tg is enhanced but toughness is decreased. A comparison of the properties of various PCTAs versus an amorphous PCT sample, prepared by quenching, are shown in Table 7.5. [Pg.286]

Method 7.3. Determination of modified acid detergent fibre (MAD fibre)... [Pg.130]

The isomorphous replacement of aluminum by gallium in the framework structure of zeolites (beta, MFI, offretite, faujasite) offers new opportunities for modified acidity and subsequently modified catalytic activity such as enhanced selectivity toward aromatic hydrocarbons [249,250]. The Ga + ions in zeolites can occupy tetrahedral framework sites (T) and nonframework cationic positions. [Pg.246]

Attin, T., Weiss, K., Becker, K., BuchaUa, W., and Wiegand, A. (2005). Impact of modified acidic soft drinks on enamel erosion. Oral Dis. 11, 7-12. [Pg.329]

Gas-liquid chromatography following reduction of paraquat to the mono- and diunsaturated derivatives (21) is of adequate sensitivity for most work when N-selective detectors are employed. Seiber and Woodrow (22.) modified this method for assaying paraquat in air samples. The method is time consuming and labor intensive, involving acid extraction and many concentration and evaporation steps. The maximum sample output per analyst per day is 6-8 with no duplicates. The reported recovery efficiency was 75% (22). although an efficiency closer to 50% is frequently encountered in practice. A modified acid extraction combined with analysis by the ELISA provides recoveries of 75% (Figure 3). This... [Pg.312]

Sandeflir, C. W. and Thomas, T. J. (1984). Modified acid dyestuff. Mobay Chemical Corp. Patent US 4 474 577. [260t]... [Pg.380]

USDA. 1996. Chemical analyses, organic carbon (6A) Walkley-Black modified acid-dichromate organic carbon (6A1) Pages 219-222. Soil survey laboratory methods manual. Soil Survey Investigations Report n 42, Version 3.0, January 1996. U.S. Department of Agriculture, Washington, D.C., USA. [Pg.184]

Alcoholysis. Methanolysis of triacylglycerols is used to prepare methyl esters for fatty acid analysis, a process frequently referred to as transesterification. This can be acid-or base-catalyzed, the method being chosen to avoid modifying acid-or base-sensitive fatty acids and to minimize reaction times. Sterol esters of fatty acids react more slowly than triacylglycerols, and samples containing them require more vigorous reaction conditions. The preparation of methyl esters from oils and fats for GC and GC-MS analysis has been extensively reviewed (19, 22, 23). [Pg.57]

There are a number of different classes of catalyst modifiers acids and bases, metal cations, nucleophilic species, and compounds with multiple bonds which are strongly chemisorbed. >54.55 a general description of each of these classes is given below. More detailed descriptions of the use of particular modifiers in specific reactions will be found in Section III. [Pg.220]

Silyl protecting groups other than TMS and TBDMS are usually applied only if a modified acid stability is wanted. Thus, the triethylsilyl (TES) group shows a sensitivity to hydrolysis and nucleophilic attack intermediate between the TMS and the TBDMS groups. The triisopropylsilyl (TIPS), ° the r-bu-tyldiphenylsilyl (TBDPS) and the thexyldimethylsilyl (TDS) groups are considerably more stable... [Pg.656]

Other ketals which are frequently used if a modified acid stability is wanted are the cyclopentylidene, the cyclohexylidene and the cycloheptylidene ketals. They are readily prepared by the reaction of a diol and the cycloalkanone in toe presence of ethyl orthoformate and mesitylenesulfonic acid. The relative rates of their acid-catalyzed hydrolysis are given in Scheme 50. [Pg.660]

The addition of organic solvents to water should modify acid-base phenomena, but assessment of such effects poses many problems, as only the measured pH of aqueous solutions can be interpreted in terms of hydrogen ion concentrations. The quantitative comparison of the acidities of partially aqueous solutions is therefore a problem of far greater complexity than the measurements of pH values in aqueous media. As mentioned earlier, a proton activity (paH) is defined in such a way that — log paH is equal to pH when the medium is water, and its value can be measured both by the electromotive force of a cell with liquid junction and by the spectrophotometry of colored indicators. [Pg.100]

The pellicle acts as a barrier, which is important in maintaining the integrity of the enamel surface by preventing demineralisation and by facilitating remineralisation. In vitro-formed pellicle has been shown to possess a selective permeability function that regulates the de- and remineralisation processes at the enamel surface [88-90], Due to its permselective nature, pellicle has the ability to modify acid diffusion and the transport of calcium and phosphate ions into and out of the enamel surface [58, 88-90], and thus is considered to play an important moderating role in the demineralisation of the enamel. However, the precise mechanism that regulates the diffusion of ions between the enamel surfaces and the oral environment in the presence of the pellicle layer is still not fully understood. [Pg.44]

Hitherto, enzymatic modification of ultrafiltered soy proteins has not been described. The present investigation shows that protein products with better properties than enzymatically modified acid precipitated proteins can be produced by a suitable combination of the involved unit operations. [Pg.134]

When a low-water biotransformation is planned, a variety of choices must be made about the precise reaction conditions to be used. As in all biocatalytic systems, the rate and yield obtained can be greatly affected by the choices made. Some of the factors that must be considered are the same as in conventional aqueous media temperature, reactant concentrations, the form in which the enzyme is added. New factors must be taken into account such as solvent selection and the level of residual water in the system. Other factors become somewhat modified acid-base conditions remain important, but, usually, pH is no longer a useful parameter to characterize them. [Pg.259]

GC-MS the modifier identity is more important than modifier concentration for enhancing extraction efficiencies of PAHs and PCBs however, the concentration influences over high molecular weight PAHs recoveries PCBs best modifiers acidic/basic modifiers including methanol, acetic acid and aniline low molecular weight PAHs best modifiers aniline, acetic acid, acetonitrile, methanol/toluene, hexane and diethylamine high molecular weight PAHs best modifiers toluene, diethylamine and methylene chloride Determination Online SFE-LC-UV extraction recovery 237... [Pg.97]


See other pages where Modifier acidic is mentioned: [Pg.472]    [Pg.813]    [Pg.19]    [Pg.86]    [Pg.19]    [Pg.212]    [Pg.66]    [Pg.291]    [Pg.480]    [Pg.39]    [Pg.288]    [Pg.246]    [Pg.142]    [Pg.1440]    [Pg.380]    [Pg.304]    [Pg.119]    [Pg.315]    [Pg.291]    [Pg.96]    [Pg.4928]    [Pg.1092]    [Pg.813]    [Pg.161]    [Pg.119]    [Pg.177]    [Pg.81]   
See also in sourсe #XX -- [ Pg.93 ]




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A-Amino acids modifying reagents

A-Hydroxy acids modifying reagents

Acetyl modified amino acids

Acid-modified

Acid-modified starches

Acidic components, enzyme-modified

Acidic modifiers/buffers

Acidic modifiers/buffers acetate buffer

Acidic modifiers/buffers acetic/formic acids

Acidic modifiers/buffers analyte retention

Acidic modifiers/buffers modifier concentration, effect

Acidic modifiers/buffers system

Acrylic acid modified glass ionomers

Acrylic acid-modified polypropylene

Aldonic acids modified

Amino acid modifying reagent

Amino acid-modified chitosan

Amino acids modified

Amino acids proteinogenic modified

Aspartic acid lithium aluminum hydride modifiers

Backbone-modified nucleic acids

Biotin-modified nucleic acid, hybridization

Carboxylic acid-modified liposomes

Cell surface presentation, modified sialic acids

Chitosan urocanic acid-modified

Crystalline amino acids modified solutions

Deoxyribonucleic acid modified

Dibasic-acid-modified PCT Copolyester Preparation and Properties

Dibasic-acid-modified PCT copolyesters

Dimer acid modifiers

Dimethyl Sulfoxide, and Common Acidic Modifiers

Fatty acid in genetically modified oilseed vegetable oils

Fatty acid in genetically modified vegetable oils

Fatty acids modified

Hyaluronic acid-modified liposomes

Hydrophobically Modified Hyaluronic Acid

Hydroxy acid modifying

Hydroxy acid modifying reagent

Lewis acid polymerization modifier

Ligand-modified nucleic acid duplexes, metal

Ligand-modified nucleic acid duplexes, metal 1 + 1] coordination

Ligand-modified nucleic acid duplexes, metal ligands

Metal tartaric acid-modified nickel

Mixed oxides modified with Lewis acids

Modified Products of Fatty Acids

Modified Products of Saturated Fatty Acids

Modified Products of Unsaturated Fatty Acids

Modified Silica Sulfuric Acid

Modified amino acids in proteins

Modified amino acids, identification

Modifying Fatty Acid Structure

Nickel Catalysts Modified with Tartaric Acid

Nucleic acids ligand-modified duplexes

Oils with Modified Fatty-Acid Content

Oxidation hydroxy acids, lead modified

Perfluorosulfonic acid modified

Platinum, lead modified acids

Poly-carboxylic acid-based modifier

Preparation variables for new nickel catalysts modified with tartaric acid

Pyruvic acid hydrogenation, modified metal catalyst

Resin-modified glass-ionomer cements acid-base reaction

Ribose-modified nucleic acids

Sialic acids modified

Stearic acid modified soy protein isolate

Surface modifiers amino-acids

Surface modifiers fatty acid salts

Surface modifiers functional organic acids

Surface modifiers polymeric acids

Tartaric Acid-Modified Nickel Catalysis

Tartaric acid modifying reagent

Tartaric acid, modifier

Thiol Modified Hyaluronic Acid

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