Chemical extraction hydrolysis

Triglyceride IDMS (for triglyceride Chemical extraction/ hydrolysis with enzymatic NA Bias<2.5% (tentative) CV<2.5% (tentative)... 

Physico-chemical treatment techniques, precipitation, sedimentation, air flotation, filtration, crystallization, chemical oxidation, wet air oxidation, super-critical water oxidation, chemical reduction, hydrolysis, nanofiltration, reserve osmosis, adsorption, ion exchange, extraction, distillation, rectification, evaporation, stripping, and incineration. 

Spectroscopic techniques have received increased attention for the study of natural organic matter (NOM) over the past decades (Hatcher et al., 2001 Abbt-Braun et al., 2004). Such techniques allow the determination of molecular speciation in many cases without the need for extractions, derivatization, or hydrolysis. Spectroscopy is generally less selective in nature than for example chemical extraction techniques, even of chemically or thermally recalcitrant compounds (Frimmel et al., 2002 Haberstroh et al., 2006), though important restrictions for specific bonds apply for some spectroscopic techniques. Equally important are the potentials to investigate the spatial relationships between NOM and mineral phases, surface properties and alteration, and micro-scale heterogeneity within NOM. With improved capabilities and access to synchrotron facilities, worldwide efforts in applying an entire range of powerful spectroscopic tools have proliferated in all areas of science. 

The enzymatic hydrolysis had also been tested as a pretreatment of chemical extraction in order to improve carotenoid recovery, and it was observed that it... 

A chemical method of extraction of nanofibers from never-dried native cellulose was developed by Saito et al. (2006) by oxidizing the surface of the nanofibers by a 2,2,6,6-tetramethylpiperidine-l-oxyl (TEMPO)-radical-catalyzed process, that requires just a posterior mechanical agitation by a Waring blender to individualize the original fibers into nanofibers of 3—5 nm in diameter. Another chemical extraction is acid hydrolysis, which ultimately produces smaller elements called cellulose... 

Bacterium seeds, water, and methanol are fed into an inoculation tank. Sterilized air and nutrients are then injected into the fermenter along with an inoculum of cultivated bacteria. Ammonia is added as a nitrogen source and for pH control Continuous fermentation produces a steady stream of bacteria, which are sent into a flocculation tank after filtration and centrifu l separation. The concentrated effluent from the flocculation tank is further dewatered by a series of decanter centrifuges. SCP destined for human consumption must under an additional step to remove the nucleic acids contained in the cells by one of the following techniques [4] (1) acid hydrolysis, (2) cell disruption, (3) chemical extraction, (4) alkaline hydrolysis, or (5) enzymatic treatment. Finalfy, the concentrated product stream is dried and processed into granules, pellets, or powder and then packed for sale. The overall yield is 1 ton protein for every 1.8 ton methanol consumed in the process. 

Isolate. A relatively pure chemical produced from natural raw materials by physical means, eg, distillation, extraction, crystallization, etc, and therefore natural or by chemical means, ie, via hydrolysis, bisulfite addition products, and regeneration, etc, and therefore artificial by 1993 U.S. labeling regulations. 

Separation Processes. The product of ore digestion contains the rare earths in the same ratio as that in which they were originally present in the ore, with few exceptions, because of the similarity in chemical properties. The various processes for separating individual rare earth from naturally occurring rare-earth mixtures essentially utilize small differences in acidity resulting from the decrease in ionic radius from lanthanum to lutetium. The acidity differences influence the solubiUties of salts, the hydrolysis of cations, and the formation of complex species so as to allow separation by fractional crystallization, fractional precipitation, ion exchange, and solvent extraction. In addition, the existence of tetravalent and divalent species for cerium and europium, respectively, is useful because the chemical behavior of these ions is markedly different from that of the trivalent species. 

The integral values of effective interfacial area can thus be obtained by measuring the reaction (extraction) rate and using physico-chemical properties of the reactants. A reaction satisfying the above conditions consists of hydrolysis of hexyl formate (11) ... 

The solubility of iridoids depends on their state (free, glycosylated, acetylated), but usually they are extracted with polar solvents methanol, ethanol, aqueous alcohols, and rarely acetone. Iridoid glycosides are more or less stable some of them are very sensitive to acids and alkalis. Some iridoid glycosides such as aucubin suffer color modification after chemical or enzymatic hydrolysis they give first a blue to green... 

The following physico-chemical properties of the analyte(s) are important in method development considerations vapor pressure, ultraviolet (UV) absorption spectrum, solubility in water and in solvents, dissociation constant(s), n-octanol/water partition coefficient, stability vs hydrolysis and possible thermal, photo- or chemical degradation. These valuable data enable the analytical chemist to develop the most promising analytical approach, drawing from the literature and from his or her experience with related analytical problems, as exemplified below. Gas chromatography (GC) methods, for example, require a measurable vapor pressure and a certain thermal stability as the analytes move as vaporized molecules within the mobile phase. On the other hand, compounds that have a high vapor pressure will require careful extract concentration by evaporation of volatile solvents. 

Several extraction techniques have also been described that use enzymatic or chemical reactions to improve extraction efficiency. A technique that has been used to increase the overall recovery of the marker residue is enzymatic hydrolysis to convert specific phase II metabolites (glucuronides or sulfates) back into the parent residue. Cooper etal used a glucuronidase to increase 10-fold the concentration of chloramphenicol residues in incurred tissue. As an example of a chemical reaction, Moghaddam et al. used Raney nickel to reduce thioether bonds between benomyl and polar cellular components, and as a result achieved a substantially improved recovery over conventional solvent extraction. In choosing to use either of these approaches, thorough characterization of the metabolism in the tissue sample must be available. 

For the purpose of the identification and quantification of additives (broadly defined) in polymeric materials extraction and dissolution methods are favoured (Sections 3.3-3.7). However, additives are also made accessible analytically by digestion of the sample matrix (cf. Section 8.2). Such wet chemical techniques, that remove the sample matrix first, are often limited to mg amounts because of pressure build-up in destruction vessels. Another reactive extraction approach to facilitate additive analysis is depolymerisation by acid hydrolysis or saponification, sometimes under pressure. This is then frequently followed by chemical methods such as titrimetry or photometry for final identification and quantification. 

Various classes of additives may undergo chemical reaction in hydrolytic conditions. For example, hydrolysis of aromatic phosphites forms phenolic compounds [645]. Additives may also undergo reaction with the polymer chain, which causes extraction difficulties. 

The urine samples were analyzed using a modified version of a published method.8 The method involved fortification of the urine samples with an internal standard 3,4,5-trichloro-2-pyridinyl, which is a structural isomer of the 3,5,6-TCP metabolite of chlorpyrifos hydrolysis of labile acid conjugates to 3,5,6-TCP solvent extraction derivitization to the f-butyl-dimethylsilyl ester of 3,5,6-TCP and subsequent negative-ion chemical ionization gas chromatography/mass spectrometry (GC/MS) analysis. Creatinine was determined in urine using a modification of a method of Fabiny and Erting-shausen.9... 

D-Pantolactone and L-pantolactone are used as chiral intermediates in chemical synthesis, whereas pantoic acid is used as a vitamin B2 complex. All can be obtained from racemic mixtures by consecutive enzymatic hydrolysis and extraction. Subsequently, the desired hydrolysed enantiomer is lactonized, extracted and crystallized (Figure 4.6). The nondesired enantiomer is reracemized and recycled into the plug-flow reactor [33,34]. Herewith, a conversion of 90-95% is reached, meaning that the resolution of racemic mixtures is an alternative to a possible chiral synthesis. The applied y-lactonase from Fusarium oxysporum in the form of resting whole cells immobilized in calcium alginate beads retains more than 90% of its initial activity even after 180 days of continuous use. The biotransformation yielding D-pantolactone in a fixed-bed reactor skips several steps here that are necessary in the chemical resolution. Hence, the illustrated process carried out by Fuji Chemical Industries Co., Ltd is an elegant way for resolution of racemic mixtures. 

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