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Chemical Converting

What if the analyte is an aqueous ion, such as Pb + In this case we cannot isolate the analyte by filtration because the Pb + is dissolved in the solution s matrix. We can still measure the analyte s mass, however, by chemically converting it to a solid form. If we suspend a pair of Pt electrodes in our solution and apply a sufficiently positive potential between them for a long enough time, we can force the reaction... [Pg.233]

Nonvolatile analytes must be chemically converted to a volatile derivative before analysis. For example, amino acids are not sufficiently volatile to analyze directly by gas chromatography. Reacting an amino acid with 1-butanol and acetyl chloride produces an esterfied amino acid. Subsequent treatment with trifluoroacetic acid gives the amino acid s volatile N-trifluoroacetyl- -butyl ester derivative. [Pg.568]

Enzymatic hydrolysis is also used for the preparation of L-amino acids. Racemic D- and L-amino acids and their acyl-derivatives obtained chemically can be resolved enzymatically to yield their natural L-forms. Aminoacylases such as that from Pispergillus OTj e specifically hydrolyze L-enantiomers of acyl-DL-amino acids. The resulting L-amino acid can be separated readily from the unchanged acyl-D form which is racemized and subjected to further hydrolysis. Several L-amino acids, eg, methionine [63-68-3], phenylalanine [63-91-2], tryptophan [73-22-3], and valine [72-18-4] have been manufactured by this process in Japan and production costs have been reduced by 40% through the appHcation of immobilized cell technology (75). Cyclohexane chloride, which is a by-product in nylon manufacture, is chemically converted to DL-amino-S-caprolactam [105-60-2] (23) which is resolved and/or racemized to (24)... [Pg.311]

Mocimycin has been chemically converted to aurodox by protection of the 4-hydroxy group at the pyridone moiety as the benzoylformate, followed by /V-methylation and hydrolytic removal of the protective group (1,55). Whereas aurodox esters are active growth promotors in animals, goldinamines that are A/-acylated by acids other than goldinonic acid, such as acetic, benzoic, or arylsulfonic acids, lack useful antimicrobial or growth-promoting activity (1). [Pg.524]

Calculate the mass or weight of chemical in the wastestream being treated by multiplying the concentration (by weight) of the chemical in the wastestream by the flow rate. In most cases, the percent removal compares the treated effluent to the influent for the particular type of wastestream. However, for some treatment methods, such as Incineration or solidification of wastewater, the percent removal of the chemical from the influent wastestream would be reported as 100 percent because the wastestream does not exist in a comparable form after treatment. Some of the treatments (e.g., fuel blending and evaporation) do not destroy, chemically convert, or physically remove the chemical from its wastestream. For these treatment methods, an efficiency of zero must be reported. [Pg.49]

For metal compounds, the calculation of the reportable concentration and treatment efficiency is based on the weight ot the parent metal, not on the weight of the metal compounds Metals are not destroyed, only physically removed or chemically converted from one form into another. The treatment efficiency reported represents only physical removal of the parent metal from the wastestream, not the percent chemical conversion of the metal compound. If a listed treatment method converts but does not remove a metal (e.g., chromium reduction), the method must be reported, but the treatment efficiency must be reported as zero. [Pg.49]

A refinery separates the many types of hydrocarbons present in cmde oils into related fractions of chemically converted, separated hydrocarbon products, and recovers the wastes that are produced. [Pg.286]

The second method used to reduce exliaust emissions incorporates postcombustion devices in the form of soot and/or ceramic catalytic converters. Some catalysts currently employ zeolite-based hydrocarbon-trapping materials acting as molecular sieves that can adsorb hydrocarbons at low temperatures and release them at high temperatures, when the catalyst operates with higher efficiency. Advances have been made in soot reduction through adoption of soot filters that chemically convert CO and unburned hydrocarbons into harmless CO, and water vapor, while trapping carbon particles in their ceramic honeycomb walls. Both soot filters and diesel catalysts remove more than 80 percent of carbon particulates from the exliatist, and reduce by more than 90 percent emissions of CO and hydrocarbons. [Pg.335]

As an alternate to LNG, natural gas can be chemically converted to methanol, chemical feedstocks (such as ethylene), gasoline, or diesel fuel. Most processes start with the conversion of methane to synthesis gas, a mixture of carbon monoxide and hydrogen. This can be done partial oxidation, an exothermic reaction ... [Pg.832]

There is not enough space here to give a detailed classification, but only to delineate the major families from which resins for industrial coatings may be selected. Resins may be divided into two groups according to their modes of film formation which may or may not involve a chemical reaction. In the first, the components must react together to form a crosslinked structure which may require heat, radiation or catalysis to effect the reaction. The bulk of resins used in industrial finishes are of this type. They are commonly referred to as chemically convertible or, simply, convertible. [Pg.673]

The rest of this section will be devoted to the chemically convertible resins. The variety of chemical types exploited in these resins are legion, so only the most widely used will be mentioned here. In some cases a single resin may be employed to produce a coating, but generally blends are used so enabling the film properties to be controlled by ratios of components as well as by choice of the components themselves. [Pg.674]

Thus, it was established that adsorption of metal hydroxide species on the surface of the substrate provides a nucleation layer which is chemically converted to the metal chalcogenide. The forming metal chalcogenide layer acts then as a catalytic surface for subsequent anion and cation adsorption. [Pg.135]

Chemical oxidation typically involves reduction/oxidation (redox) reactions that chemically convert hazardous contaminants to nonhazardous or less toxic compounds that are more stable, less mobile, or inert. Redox reactions involve the transfer of electrons from one compound to another. Specifically, one reactant is oxidized (loses electrons) and one is reduced (gains electrons). The oxidizing agents... [Pg.624]

Achiral lanthanide shifting reagents may be used to enhance the anisochrony of diastereomeric mixtures to facilitate their quantitative analysis. Chiral lanthanide shift reagents are much more commonly used to quantitatively analyze enantiomer compositions. Sometimes it may be necessary to chemically convert the enantiomer mixtures to their derivatives in order to get reasonable peak separation with chiral chemical shift reagents. [Pg.21]

Although most ethanol is now produced from corn, research has been done on producing this type of alcohol fuel from cellulosic biomass products including energy crops, forest and agricultural residues, and MSW, which would provide much cheaper feedstocks. The process of chemically converting these cellulosic biomass feedstocks is more involved and until this process can be simplified the price of ethanol will remain high. [Pg.22]

Mercury is the only metal that is a liquid at ordinary temperatures. It is therefore also the only metal that has a significant vapor pressure at ordinary temperatures. For this reason, it is possible to obtain mercury atoms in the gas phase for measurement by atomic absorption without the use of thermal energy. It is a matter of chemically converting mercury ions in the sample into elemental mercury, getting it in the gas phase, and channeling it into the path of the light of an atomic absorption instrument. [Pg.266]

Humans have a limited capacity to synthesize amino acids de novo, but extensive interconversions can occur. Those amino acids which cannot be formed within the body and must be supplied by the diet are called essential . Members of this group, which includes the branched chain amino acids leucine and valine, and also methionine and phenylalanine, are all dietary requirements. Such essential amino acids may be chemically converted, mainly in the liver, into the non-essential amino acids. The term non-essential does not equate with not biochemically important but simply means they are not strict dietary components. [Pg.172]

J.R. Lomeda, C.D. Doyie, D. V Kosynkin, W.-F. Hwang, J.M. Tour, Diazonium functionalization of surfactant-wrapped chemically converted graphene sheets, Journal of the American Chemical Society, 130 (2008) 16201-16206. [Pg.38]

H. F. Yang, C. S. Shan, F.H. Li, D.X. Han, Q. X. Zhang, L. Niu, Covalent functionalization of polydisperse chemically-converted graphene sheets with amine-terminated ionic liquid, Chemical Communications, vol. 26, pp. 3880-3882, 2009. [Pg.113]

Indians. The active principle, salicin, was isolated in 1829. It is chemically converted to the active principle, salicylic acid, in the intestine and liver. The chemically modified acetylsalicylic acid was first marketed in 1899 as aspirin. Salicin is also found in meadowsweet (Filipenduia ulmaria, then referred to as Spireaea ulmaria), from which the name aspirin derives (acetyl sp/r/c acid). The sodium salt of salicylic acid has the drawback of producing gastrointestinal irritation, but acetylsalicylic acid is well tolerated. [Pg.318]

A potential versatile route into a-amino acids and their derivatives is via a combination of (i) nitrile hydratase/amidase-mediated conversion of substituted malo-nonitriles to the corresponding amide/acid followed by (ii) stereospecific Hofmann rearrangement of the amide group to the corresponding amine. Using a series of a,a-disubstituted malononitriles 14, cyanocarboxamides 15 and bis-carboxamides 16, the substrate specificity of the nitrile hydratase and amidase from Rhodococcus rhodochrous IF015564 was initially examined (Scheme 2.7). The amidase hydrolyzed the diamide 16 to produce (R)-17 with 95% conversion and 98%e.e. Amide 17 was then chemically converted to a precursor of (S)-a-methyldopa. It was found... [Pg.26]

The biodegradable polymer available in the market today in largest amounts is PEA. PEA is a melt-processible thermoplastic polymer based completely on renewable resources. The manufacture of PEA includes one fermentation step followed by several chemical transformations. The typical annually renewable raw material source is com starch, which is broken down to unrefined dextrose. This sugar is then subjected to a fermentative transformation to lactic acid (LA). Direct polycondensation of LA is possible, but usually LA is first chemically converted to lactide, a cyclic dimer of LA, via a PLA prepolymer. Finally, after purification, lactide is subjected to a ring-opening polymerization to yield PLA [13-17]. [Pg.110]

In 1980, in collaboration with Professor Ohno, Faculty of Phanmaceutical Sciences, the University of Tol o, we were successful in the chemical synthesis of pyrimidoblamic acid (84). This was one of the most important parts of the total synthesis of bleomycin. Soon therecifter. Dr. Takita et (55) in my institute were successful in the synthesis of the entire peptide peu t of bleomycin A2 1981 and then in the total synthesis of bleomycin A2 in the same year (56,54). Before this, we chemically converted bleomycin A2 to bleomycin demethyl A2 and estcibllshed synthetic processes for preparing bleonycinic acid from bleomycin demethyl A2 and for preparing various bleomycins from bleonycinic acid (62). Thus, the structures of bleomycins shown in Fig. 4 were conclusively estcibllshed. After our synthesis, Hecht al.also reported on the synthesis of the deglycobleomycin demethyl A2 (3) and the synthesis of bleomycin demethyl A2 (1). [Pg.77]

The desired nucleotides are produced directly by fermentation in concentrations above 30 g L h IMP or inosine, which can be chemically converted into... [Pg.516]

IMP, is synthesised with mutants of Bacillus subtilis or Corynehacterium am-moniagenes. Xanthosine 5 -monophosphate is produced with Corynebacte-rium or Bacillus and subsequently converted into GMF by Bacillus and other strains [6]. Alternatively, another related compound, 5 -amino-4-imidazole carboxamide-l-riboside-5 -phosphate, is produced by Bacillus megaterium and chemically converted into GMP [22, 36],... [Pg.517]


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