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Linear broad-standard

Establishing a calibration function with one single broad distributed sample is an alternative to traditional peak postion calibration of SEC systems with a set of narrow distributed standards. An obvious advantage of this technique is time for peak position calibration elution profiles for the set of standards need to be determined for broad standard calibration the elution profile of one sample needs to be determined only. Establishing a linear calibration function with a broad distributed standard includes startup information [M (true), Mn(true)] and an iterative (repeat.. . until) algorithm ... [Pg.463]

FIGURE 16.5 Broad standard calibration (linear mode) of a semipreparative Sephacryl S-IOOO system (95 x 1.6 cm) with an aqueous mixture of Blue Dextran, Dextran T-SOO, and glucose eluent 0.005 M NaOH V, i = 75 ml. = 162 ml. [Pg.470]

An added benefit of the direct SEC-[n] calibration approach is that a new independent way of determining K and a values, using only broad MW standards, has also resulted. As few as three standards (or four, if all are narrow MWD) are needed to obtain both MW and [x]] calibration curves for a particular polymer-solvent system by using the broad-standard, linear calibration approach. From the experimental calibration constants of the two calibration curves, one can calculate K and a directly as described later. [Pg.92]

C. Linear SEC-[nl Calibration Using Broad Standards. It is to be noted that the viscosity calibration curve in Figure 3 is essentially linear. This linearity is derived from bimodal SEC column sets. [Pg.99]

The broad-standard linear calibration curves for polystyrene in THF in Figure 1 and 4 are used to illustrate the K and a calculations as follows. The particular calibration curves are found to correspond to the following calibration equations ... [Pg.104]

Several assumptions were made in using the broad MWD standard approach for calibration. With some justification a two parameter equation was used for calibration however the method did not correct or necessarily account for peak speading and viscosity effects. Also, a uniform chain structure was assumed whereas in reality the polymer may be a mixture of branched and linear chains. To accurately evaluate the MWD the polymer chain structure should be defined and hydrolysis effects must be totally eliminated. Work is currently underway in our laboratory to fractionate a low conversion polydlchlorophosphazene to obtain linear polymer standards. The standards will be used in polymer solution and structure studies and for SEC calibration. Finally, the universal calibration theory will be tested and then applied to estimate the extent of branching in other polydlchlorophosphazenes. [Pg.252]

Preparation of the GPC system, especially the performance of the viscometric detection and the performance of the refractometer DRI prototype ( 4), was performed by the comparison of the viscosity law obtained using the TSK narrow standards represented in Figure 2 and the one obtained with a linear broad polymer, like the polystyrene Dow 1683 (Dow Chemical,... [Pg.170]

GPC s of the diree resins are shown in Figure 7 and are calibrated relative to linear polystyrene standards. All of the resin samples are low molecular weight with relatively broad polydiqiersities. Given the inappropriate nature of the linear polystyrene GPC standards for SSQ derivatives, e data in Figure 7 are usefiil for relative comparison only. [Pg.149]

An alternative method of calibrating a size elution chromatographic instrument that uses only a concentration-sensitive detector is to use a broad molecular weight sample for which the molecular weight distribution is accurately known. Such a linear polyethylene standard is available from the National Institute of Standards and Technology (in the United States). However, this standard does not cover a sufficient range to encompass the complete range of commercial polyethylene resins. [Pg.246]

Use of Multiple Broad Molecular Weight Distribution Standards for Linear Polymers... [Pg.183]

Those which employ one or more broad MWD standards with known M or [n] and assume a linear molecular weight calibration curve and finally those which employ one broad MWD... [Pg.183]

Methods based on universal calibration will be illustrated using nonaqueous SEC and broad MWD PVC standards. The and of these standards is known. Methods based on the linear molecular weight calibration will be illustrated using aqueous SEC and broad MTO polydextran standards for which M and My are known. [Pg.188]

Figure 4. Molecular weight calibration curves for polydextran obtaimd u g linear calibration and two broad M WD standards and by plotting Mrm ( / Mif Mw) vs, peak retention volume ((%) Mrms, (---------) M(v) = 0,37 X exp(—OJ v))... Figure 4. Molecular weight calibration curves for polydextran obtaimd u g linear calibration and two broad M WD standards and by plotting Mrm ( / Mif Mw) vs, peak retention volume ((%) Mrms, (---------) M(v) = 0,37 X exp(—OJ v))...
Table V. Results of Case Study 2 - Linear Calibration with Two Broad MWD Polydextran Standards with Known Mj and... Table V. Results of Case Study 2 - Linear Calibration with Two Broad MWD Polydextran Standards with Known Mj and...
Dow 1683 polystyrene standard was utilized as a broad MWD standard in the linear calibration method due to its distribution symmetry and particular lack of significant tail at the low end of its MWD. [Pg.78]


See other pages where Linear broad-standard is mentioned: [Pg.469]    [Pg.469]    [Pg.462]    [Pg.93]    [Pg.99]    [Pg.330]    [Pg.332]    [Pg.84]    [Pg.88]    [Pg.104]    [Pg.108]    [Pg.345]    [Pg.1574]    [Pg.420]    [Pg.495]    [Pg.332]    [Pg.448]    [Pg.463]    [Pg.180]    [Pg.187]    [Pg.68]    [Pg.265]    [Pg.665]    [Pg.111]    [Pg.197]    [Pg.119]    [Pg.142]    [Pg.357]    [Pg.286]    [Pg.73]    [Pg.74]    [Pg.74]    [Pg.75]    [Pg.78]    [Pg.80]    [Pg.83]   
See also in sourсe #XX -- [ Pg.104 ]




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