Refractive Index RI

Refractive Index. The effect of mol wt (1400-4000) on the refractive index (RI) increment of PPG in ben2ene has been measured (167). The RI increments of polyglycols containing aUphatic ether moieties are negative drj/dc (mL/g) = —0.055. A plot of RI vs 1/Af is linear and approaches the value for PO itself (109). The RI, density, and viscosity of PPG—salt complexes, which maybe useful as polymer electrolytes in batteries and fuel cells have been measured (168). The variation of RI with temperature and salt concentration was measured for complexes formed with PPG and some sodium and lithium salts. Generally, the RI decreases with temperature, with the rate of change increasing as the concentration increases. 

Another classification of detector is the bulk-property detector, one that measures a change in some overall property of the system of mobile phase plus sample. The most commonly used bulk-property detector is the refractive-index (RI) detector. The RI detector, the closest thing to a universal detector in lc, monitors the difference between the refractive index of the effluent from the column and pure solvent. These detectors are not very good for detection of materials at low concentrations. Moreover, they are sensitive to fluctuations in temperature. 

Similar to aniline point, refractive index (RI) shows how refractive or aromatic a sample is. The higher the RI, the more the aromatics and the less crackable the sample. A feed having an RI of 1.5105 is more difficult to crack than a feed with an RI of 1.4990. The RI can be measured in a lab (ASTM D-1218) or predicted using correlations such as the one published by TOTAL. 

Refractive Index is used to analyse the sample. It can also be used to help determine the percentage of a chemical (such as ethanol) in an aqueous solution. Refractive index (RI) is always reported to four decimal places. An example of the RI scale is shown in Figure 10.4. The correct reading from the RI of the sample would be 1.3764. 

Many different detectors are used in RPLC, including ultraviolet-visible spectrophotometers (UV-VIS), refractive index (RI) detectors, electrochemical (EC) detectors, evaporative light-scattering detectors, fluorimeters, and... 

Detection in 2DLC is the same as encountered in one-dimensional HPLC. A variety of detectors are presented in Table 5.2. The choice of detector is dependent on the molecule being detected, the problem being solved, and the separation mode used for the second dimension. If MS detection is utilized, then volatile buffers are typically used in the second-dimension separation. Ultraviolet detection is used for peptides, proteins, and any molecules that contain an appropriate chromophore. Evaporative light scattering detection has become popular for the analysis of polymers and surfactants that do not contain UV chromophores. Refractive index (RI) detection is generally used with size exclusion chromatography for the analysis of polymers. 

The results summarized above were obtained by using fluorescence based assays employing phospholipid vesicles and fluorescent labeled lipopeptides. Recently, surface plasmon resonance (SPR) was developed as new a technique for the study of membrane association of lipidated peptides. Thus, artificial membranes on the surface of biosensors offered new tools for the study of lipopeptides. In SPR (surface plasmon resonance) systemsI713bl changes of the refractive index (RI) in the proximity of the sensor layer are monitored. In a commercial BIAcore system1341 the resonance signal is proportional to the mass of macromolecules bound to the membrane and allows analysis with a time resolution of seconds. Vesicles of defined size distribution were prepared from mixtures of lipids and biotinylated lipopeptides by extruder technique and fused with a alkane thiol surface of a hydrophobic SPR sensor. 

Refraction phenomena, nonlinear, 17 454 Refractive index (RI), 11 131 15 187 of compound semiconductors, 22 150t, 151... 

Five different detectors are common in HPLC (1) UV, (2) refractive index (RI), (3) conductivity, (4) inductively coupled plasma atomic emission, and (5) mass spectrometry. A UV detector passes a specific wavelength of UV light... 

Density measured at the same temperature as the refractive index RI... 

Light from the source(s) is focused into the cell, that consists of sample and reference sample and the two chambers are separated by a diagonal sheet of glass. After passing through the cell, the light is diverted by a beam-splitter (B) to two photocells (Pj and P2 respectively. A change in the observed refractive index (RI) of the sample stream causes a difference in their relative output, which is adequately amplified and recorded duly. 

As the analyte or any other species that may be present changes in concentration, the refractive index (RI) of the sample medium also changes. A large change in the RI may interfere with the fluorescent signal because the numerical aperture of the fiber is proportional to the RI as shown in the relation below ... 

However, samples that have no UV absorbance, exist in ionic form, or require structural information have to couple with other types of detectors. Refractive index (RI) detector is almost a universal detector in that it responds to almost any solute (UV-absorbing molecules, sugars,... 

Since the development of HPLC as a separation technique, considerable effort has been spent on the design and improvement of suitable detectors. The detector is perhaps the second-most important component of an HPLC system, after the column that performs the actual separation it would be pointless to perform any separation without some means of identifying the separated components. To this end, a number of analytical techniques have been employed to examine either samples taken from a fraction collector or the column effluent itself. Although many different physical principles have been examined for their potential as chromatography detectors, only four main types of detectors have obtained almost universal application, namely, ultraviolet (UV) absorbance, refractive index (RI), fluorescence, and conductivity detectors. Today, these detectors are used in about 80% of all separations. Newer varieties of detector such as the laser-induced fluorescence (LIE), electrochemical (EC), evaporative light scattering (ELS), and mass spectrometer (MS) detectors have been developed to meet the demands set by either specialized analyses or by miniaturization. 

All reactions were run in a Parr stirred autoclave (Model 4561) at 1000 psi H2 and 200°C for 6h. A weighed quantity (0.5 g dry basis) of the catalyst, Ru/C or Ni/Re/C, was introduced into the reactor and reduced at 250 C and 200 psi H2 (Ru/C) or at 280°C and 500 psi H2 (Ni/Re/C) for 13 hours. After cooling, 100ml of solution (l.OM GO and O.l-l.OM KOH) was added to the closed reactor. For reactions in solvent mixtures, entries 1-4 in Table 2, the water/solvent ratio was 1/9 (v/v). When the solvent was either t-BuOH or 1,4-dioxane, 1.5 g of water was added to the solution to facilitate dissolution of KOH, because of its low solubility these solvents. Once steady state was achieved following heatup, samples were taken at 30 minute intervals for the first hour, and then hourly, and analyzed via HPLC. The HPLC column was a BIORAD Aminex HPX-87H run at 65 C with 5mM H2SO4 as the mobile phase at a flow rate of 0.6mFmin, using both UV (210 nm) and refractive index (RI) detection. 

GPC is a relative method, especially for UV and refractive index (RI) detectors, and must be calibrated using polymer standards whose molecular weight has been determined using absolute methods such as intrinsic viscosity or light scattering. Consequently, the accuracy is relative to the calibration. 

GPC Analysis. Molecular weight characterizations were carried out using a Waters 840 Gel Permeation Chromatograph equipped with both an ultraviolet (UV) (Model 481) and a refractive index (RI) detector (Model 410). Two Ultrastyragel columns, in the running order of 1,000 and 10,OOOA pore... 

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