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Additive preparation

Prepare a solution of each additive as specified by the manufacturer and/or as discussed below, filter-sterilize the solution and add to the sterile culture medium. [Pg.211]


MSG, C8H8NNa04,H20. Flavouring agent extensively used as a food additive. Prepared from natural or synthetic L-glutamic acid. [Pg.364]

Procedure. Prepare a set of external standards containing 0.5 g/L to 3.0 g/L creatinine (in 5 mM H2SO4) using a stock solution of 10.00 g/L creatinine in 5 mM H2SO4. In addition, prepare a solution of 1.00 x 10 M sodium picrate. Pipet 25.00 mL of 0.20 M NaOH, adjusted to an ionic strength of 1.00 M using Na2S04, into a thermostated reaction cell at 25 °C. Add 0.500 mL of the 1.00 x 10 M picrate solution to the reaction cell. Suspend a picrate ion-selective electrode in the solution, and monitor the potential until it stabilizes. When the potential is stable, add 2.00 mL of a... [Pg.632]

Usually, the ore or concentrate cannot be reduced to the metal in a single operation. An additional preparation process is needed to modify the physical or chemical properties of the raw material prior to its reduction. Furthermore, most pyrometaHurgical reductions do not yield a pure metal and an additional step, refining, is needed to achieve the chemical purity that is specified for the commercial use of the metal. [Pg.164]

Lakes. Lakes are a special kind of color additive prepared by precipitating a soluble dye onto an approved iasoluble base or substratum. In the case of D C and Ext. D C lakes, this substratum may be alumina, blanc fixe, gloss white, clay, titanium dioxide, 2iac oxide, talc, rosia, aluminum ben2oate, calcium carbonate, or any combination of two or more of these materials. Currentiy, alumina is the only substratum approved for manufactuting FD C lakes. [Pg.444]

The accuracy and precision of carotenoid quantification by HPLC depend on the standard purity and measurement of the peak areas thus quantification of overlapping peaks can cause high variation of peak areas. In addition, preparation and dilution of standard and sample solutions are among the main causes of error in quantitative analysis. For example, the absorbance levels at of lutein in concentrations up to 10 mM have a linear relationship between concentration and absorbance in hexane and MeOH on the other hand, the absorbance of P-carotene in hexane increased linearly with increasing concentration, whereas in MeOH, its absorbance increased linearly up to 5 mM but non-linearly at increasingly higher concentrations. In other words, when a stock solution of carotenoids is prepared, care should be taken to ensure that the compounds are fuUy soluble at the desired concentrations in a particular solvent. [Pg.471]

P. F. Tsytsymushkin, S. R. Khajmllin, A. P. Tamavskij, Z. N. Kudryashova, P. V. Kovalenko, V. N. Levshin, and B. V. Mikhajlov. Plugging solution for cementing oil and gas wells in salt-bearing strata—contains plugging cement, sodium chloride, calcium chloride, additional preparate bakteritsid, and water. Patent SU 1803531-A, 1993. [Pg.471]

Formation of polynuclear lead species with parameters close to isolated lead bromophenoxides during DPC synthesis was found by EXAFS of frozen active reaction mixtures (Pb-0 = 2.34 A, Pb Pb = 3.83 A). Noteworthy, in samples of final reaction mixtures, where catalyst was inactive, short Pb Pb distances were absent. These polynuclear compounds have been tested as lead sources in large-scale runs (small scale reactions were inconclusive due to heterogeneity of reaction mixtures because these compounds are less soluble than PbO). It was found that the use of lead bromophenoxides instead of PbO increases both Pd TON (by 25-35%), and reaction selectivity (from 65 - 67 % to 75 - 84 %). Activity of different lead bromophenoxides was about the same (within experimental error) but the best selectivity was observed for complex Pb602(0Ph)6Br2. Therefore, the gain in selectivity vs. loss due to additional preparation step should be analyzed for practical application. [Pg.191]

Additional preparations of this type utilize 2-(cyanomethyl)pyridine. As shown in Scheme 4, condensation of this reagent with pyrimidine 84 gives pyrimidoquinolizine 86 through intermediary of 85 <2002T5733>. [Pg.1017]

Coordination compounds have been produced by a variety of techniques for at least two centuries. Zeise s salt, K[Pt(C2H4)Cl3], dates from the early 1800s, and Werner s classic syntheses of cobalt complexes were described over a century ago. Synthetic techniques used to prepare coordination compounds range from simply mixing the reactants to employing nonaqueous solvent chemistry. In this section, a brief overview of some types of general synthetic procedures will be presented. In Chapter 21, a survey of the organometallic chemistry of transition metals will be presented, and additional preparative methods for complexes of that type will be described there. [Pg.695]

Fresh-cut fruits and vegetables are products that are partially prepared so that no additional preparation is necessary for their use (Ayala-Zavala and others 2008a). They are prepared for restaurants, fast food outlets, and retail markets. Fresh-cut is also defined as any fruit or vegetable or combination that has been trimmed, peeled, washed, and cut into 100% useable product that is then bagged or prepackaged and remains in a fresh state (Lamikanra 2002). [Pg.316]

For quantitative analysis, the amount of sample taken is usually measured by mass or volume. Where a homogeneous sample already exists, it may be subdivided without further treatment. With many solids such as ores, however, crushing and mixing are prior requirements. The sample often needs additional preparation for analysis, such as drying, ignition and dissolution. [Pg.614]

Samples are dissolved in water to a concentration of approximately 0.5 mg/ml and injected directly into the liquid chromatograph without additional preparation. The conditions of section 6.5.3 apply also to the analysis of formulations. ... [Pg.157]

Double-sided electrolytic contacts are favorable for this method of diffusion length measurement because they are transparent and the required SCRs are easily induced by application of a reverse bias. Therefore homogeneously doped wafers need no additional preparation, such as evaporation of metal contacts or diffusion doping, to produce a p-n junction. Furthermore, a record low value of surface recombination velocity has been measured for silicon surfaces in contact with an HF electrolyte at OCP [Yal], Note that this OCP value cannot be further decreased by a forward bias at the frontside, because any potential other than OCP has been found to increase the surface recombination velocity, as shown in Fig. 3.2. Note that contaminations in the HF electrolyte, such as Cu, may significantly increase the surface recombination velocity. This effect has been used to detect trace levels (20 ppt) of Cu in HF [Re5j. [Pg.214]

Cryoelectron microscopy makes it possible to have a direct view into the frozen sample without additional preparation [100]. With the aid of a cryogen (e.g., liquid nitrogen-cooled liquid ethane), the sample is plunge frozen as a very thin aqueous film prepared on a microscopic grid. Subsequently, the vitrified specimen is directly transferred into a precooled electron microscope. Because the specimens are usually ) 2005 by CRC Press LLC... [Pg.15]

APROTIC DOUBLE MICHAEL ADDITION PREPARATION OF 1,3-DIMETHYL-5-OXOBICYCLO[2.2.2]OCTANE-2-CAR80XYLIC ACID... [Pg.271]

The JECFA expert assigned the responsibility for preparing the specifications for identity and purity for the food additive prepares a Chemical and Technical Assessment (CTA) document. The CTA contains the chemistry, manufacturing process, technological justification, and intended use of the food additive (FAO CTA Guideline, 2003) (12). The CTD guideline should be used for submission of chemical and technical information to JECFA. [Pg.73]

Additional Preparative-Scale HPLC Separations. After mutagenesis assessment of the HPLC fractions from the initial preparative-scale separation just discussed, those fractions containing mutagenic constituents are further separated on HPLC by employing the following strategy For example, if the mutagenic constituents were found to be in Fraction D from an initial reverse-phase HPLC preparative-scale separation, that is, a mobile-phase composition of 25 water 75 acetonitrile, a... [Pg.400]

Finally, all the additives prepared by hydroperoxide intermediates increase dramatically the life time (both in photo and thermal ageing) of elastomers such as EPDM(ENB) and polyoctenamer whose the original stabilities are well known to be very low. [Pg.20]

Although the size and shape of proteins can have some influence on solubility properties, the chief method of exploiting these properties is gel-filtration chromatography. In addition, preparative gel electrophoresis makes use of differences in molecular size. Proteins range in size from the smallest classified as proteins rather than polypeptides, around 5000 Da, up to macromolecular complexes of many million daltons. Many proteins in the bioactive state are oligomers of more than one polypeptide (see below), and these can be dissociated, though normally with loss of overall structure. Thus many proteins have two sizes that of the native state, and that (or those) of the polypeptides in the denatured and dissociated state. Gel-filtration procedures normally deal only with native proteins, whereas electrophoretic procedures commonly involve separation of dissociated and denatured polypeptides. [Pg.272]

See also page 410, Section 2, for additional preparations of vinylic halides. [Pg.655]

A 1,3-dipolar cycloaddition of indanoneenamines and nitrilimines produces the indeno[2,1 -cjpyrazole (52).135 The yields of such cyclization reactions are high (60-80%). Reactions of A-alkylpyridine-3-ylides with picryl chloride involving cyclization give a mixture of pseudoazulenes 35 and 36.103 An additional preparation of pyrindine 26 is from 1,2- and 1,4-oxides of azonine.55... [Pg.216]

Distribution of solutes throughout the matrix can also affect the extraction process. The analytes can be adsorbed on the matrix surface or encapsulated in the matrix. Encapsulated analytes may require harsher extraction conditions or additional preparation steps such as grinding or chopping, prior to extraction. Once this information is collected the chemist can address the problem of developing the extraction method. [Pg.255]

Gold solution for additions prepare a gold 2.0 x 10-5 M solution in 0.1 M HC1 from the gold standard solution. [Pg.1267]

The additive, prepared from iron sulfate [Fe2(S04)3], is used to promote hydrogenation and effectively eliminate coke formation. The effectiveness of the dual-role additive permits the use of operating temperatures that give high conversion in a single stage reactor. The process maximizes the use of reactor volume and provides a thermally stable operation with no possibility of temperature runaway. [Pg.362]

As we have shown earlier, survey studies and studies of clinical samples have provided a large body of evidence relating inadequate or disturbed sleep to various measures of functioning. Very few studies, however, have employed experimental designs to study consequences of inadequate or restricted sleep. Parents are often reluctant for their children to lose sleep or to stay overnight in a laboratory. In addition, preparing laboratory and staff for the needs of children adds another layer of complexity to laboratory studies. The few experimental studies have provided mixed results and much more research is required. New evidence that school-age children can comply with imposed sleep schedules at home for days and weeks may facilitate additional studies (137). [Pg.166]

Stereocontrolled construction of the natural configuration 327 at C-20 in steroid side-chains is an important problem in steroid synthesis. In addition, preparation of the... [Pg.140]

Ekstrom, T., Falk, L.K.L. and Knutson-Wedel, E.M., (1991), Si3N4-Zr02 composites with small A1203 and Y203 additions prepared by HIP , J. Mater. Sci., 26(16), 4331-4340. [Pg.511]

Comparison of silicon nitrides with carbon additions prepared by hot isostatic pressing and pressureless sintering... [Pg.518]


See other pages where Additive preparation is mentioned: [Pg.1578]    [Pg.348]    [Pg.1007]    [Pg.572]    [Pg.1007]    [Pg.136]    [Pg.355]    [Pg.1316]    [Pg.66]    [Pg.389]    [Pg.248]    [Pg.423]    [Pg.86]    [Pg.37]    [Pg.1]    [Pg.85]    [Pg.508]    [Pg.348]    [Pg.170]    [Pg.218]   


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