Spectrophotometers difference

For the purposes of chemical oceanography, spectrophotometry is limited to wavelengths from the UV to near-IR (250 to 1500 nanometers). The various forms of spectrophotometer differ primarily in combinations of light sources, dispersive elements, and detectors. 

There are a variety of instruments available for the measurement of colour. Colorimeters usually determine the proportions of the primary additive lights which are necessary to match the colour reflected or transmitted by the sample under investigation. Spectrophotometers differ in that they record the intensity of the reflected light continuously over the whole spectral range. 

Absolute and differential absorption spectra were obtained on a Hewlett-Packard photodiode array spectrophotometer. Difference spectra were generated by subtracting the absorbance spectra of the test solution from the initial effluent and then subtracting the absorbance spectra of the solution surrounding the cells containing BA from its counterpart which did not contain BA. Difference spectra generated for (1) the dye solution with and without BA and (2) the initial effluent over time, show no absorbance differences. In addition, spectra were run of dye solution with known [Ca ] to generate a standard curve. 

Describe how a monochromator, a spectrograph, and a spectrophotometer differ from each other. 

Atomic absorption spectrophotometers (Figure 10.37) are designed using either the single-beam or double-beam optics described earlier for molecular absorption spectrophotometers (see Figures 10.25 and 10.26). There are, however, several important differences that are considered in this section. 

Atomization The most important difference between a spectrophotometer for atomic absorption and one for molecular absorption is the need to convert the analyte into a free atom. The process of converting an analyte in solid, liquid, or solution form to a free gaseous atom is called atomization. In most cases the sample containing the analyte undergoes some form of sample preparation that leaves the analyte in an organic or aqueous solution. For this reason, only the introduction of solution samples is considered in this text. Two general methods of atomization are used flame atomization and electrothermal atomization. A few elements are atomized using other methods. 

As a result of these considerations, the primary difference between a spectrophotometer and a light-scattering photometer is the fact that the photodetector is mounted on an arm which pivots at the sample so that intensity measurements can be made at various angles. 

The science of color measurement has been explored by various authors (127,128). AATCC evaluation procedure no. 6 describes a method for instmmental measurement of color of a textile fabric. AATCC evaluation procedure no. 7 may be used to determine the color difference between two fabrics of a similar shade. Instmmentation may be either a spectrophotometer for measuring reflectance versus wavelength, or a colorimeter for measuring tristimulus values under specified illumination. If a spectrophotometer is used, however, the instmment must be equipped with tristimulus integrators capable of producing data in terms of CIE X, Y, and Z tristimulus values. 

The comparison of more than two means is a situation that often arises in analytical chemistry. It may be useful, for example, to compare (a) the mean results obtained from different spectrophotometers all using the same analytical sample (b) the performance of a number of analysts using the same titration method. In the latter example assume that three analysts, using the same solutions, each perform four replicate titrations. In this case there are two possible sources of error (a) the random error associated with replicate measurements and (b) the variation that may arise between the individual analysts. These variations may be calculated and their effects estimated by a statistical method known as the Analysis of Variance (ANOVA), where the... 

Procedure. Dissolve a weighed portion of the substance in which the amount of iron is to be determined in a suitable acid, and evaporate nearly to dryness to expel excess of acid. Dilute slightly with water, oxidise the iron to the iron(III) state with dilute potassium permanganate solution or with a little bromine water, and make up the liquid to 500 mL or other suitable volume. Take 40 mL of this solution and place in a 50 mL graduated flask, add 5 mL of the thiocyanate solution and 3 mL of AM nitric acid. Add de-ionised water to dilute to the mark. Prepare a blank using the same quantities of reagents. Measure the absorbance of the sample solution in a spectrophotometer at 480 nm (blue-green filter). Determine the concentration of this solution by comparison with values on a reference curve obtained in the same way from different concentrations of the standard iron solution. 

Traditional infrared spectrophotometers were constructed with mono-chromation being carried out using sodium chloride or potassium bromide prisms, but these had the disadvantage that the prisms are hygroscopic and the middle-infrared region normally necessitated the use of two different prisms in order to obtain adequate dispersion over the whole range. 

Photoelectric-Colorimetric Method. Although the recording spectrophotometer is, for food work at least, a research tool, another instrument, the Hunter multipurpose reflectometer (4), is available and may prove to be applicable to industrial quality control. (The newer Hunter color and color difference meter which eliminates considerable calculation will probably be even more directly applicable. Another make of reflection meter has recently been made available commercially that uses filters similar to those developed by Hunter and can be used to obtain a similar type of data.) This instrument is not a spectrophotometer, for it does not primarily measure the variation of any property of samples with respect to wave length, but certain colorimetric indexes are calculated from separate readings with amber, blue, and green filters, designated A, B, and G, respectively. The most useful indexes in food color work obtainable with this type of instrument have been G, which gives a... 

With the best observing conditions, it is possible for the trained observer to compete with photoelectric colorimeters for detection of small color differences in samples which can be observed simultaneously. However, the human observer cannot ordinarily make accurate color comparisons over a period of time if memory of sample color is involved. This factor and others, such as variability among observers and color blindness, make it important to control or eliminate the subjective factor in color grading. In this respect, objective methods, which make use of instruments such as spectrophotometers or carefully calibrated colorimeters with conditions of observation carefully standardized, provide the most reliable means of obtaining precise color measurements. 

Two identical reaction solutions were prepared, one at T,(= 25.000 °C) in the sample compartment of a double-beam spectrophotometer, the other at T2( = 27.170 °C) in the reference beam. A direct recording of AAbs = Absi - Abs2 was made as a function of time while the difference in reaction temperature was maintained to 0.0001 °C. Evaluate kffk and AW1 for the run shown note this calculation is possible with an arbitrary time axis. 

The sampling of solution for activity measurement is carried out by filtration with 0.22 pm Millex filter (Millipore Co.) which is encapsuled and attached to a syringe for handy operation. The randomly selected filtrates are further passed through Amicon Centriflo membrane filter (CF-25) of 2 nm pore size. The activities measured for the filtrates from the two different pore sizes are observed to be identical within experimental error. Activities are measured by a liquid scintillation counter. For each sample solution, triplicate samplings and activity measurements are undertaken and the average of three values is used for calculation. Absorption spectra of experimental solutions are measured using a Beckman UV 5260 spectrophotometer for the analysis of oxidation states of dissolved Pu ions. 

This olefin was chosen because its slow bromination rate allows to make accurate measurements of transient CTC s with a conventional spectrophotometer. Curve d is a difference spectrum between a solution of Bi2 plus a hundred fold excess of olefin (curve c) and those of the single reagents (curves a and b), and represents the tail of the expected CT band. From the linearity of the plots of the difference absorbance agains the olefin concentration (Fig. 2) it was possible to evaluate a limiting value of Kf < 0.1 M l. On the other hand, a AH = - 0.9 kcal moTl was obtained from a plot (Fig. 3) of the in of the products KfScx. obtained from the first plot, against 1/T, assuming ecj to be temperature independent (ref. 3). 

Nearly all methemoglobln variants exhibit absorption spectra that are different from that of normal ferrlhemoglobln The absorption spectra are determined after the hemolysate Is dialyzed overnight at 4 0 against an 0 1 M phosphate buffer, pH 6 4 or 7 1, using an automatic recording spectrophotometer ... 

Amotf was the first to develop a set of equations for acetone to simultaneously calculate chlorophyll a and chlorophyll b in 1949. Several authors later proposed different new equations based on more adjusted and accurate extinction coefficients due to the development of higher resolution spectrophotometers adapted to each special condition. Moreover, besides 80% acetone, coefficients for diethyl ether and ethanol were also established and their respective equations developed, as reviewed by Schwartz and Lorenzo and Eder. Solvents chosen should be those for which specific absorbance coefficients have been published to derive equations and updates should be carefully tracked for new values. 

The infrared absorbance spectra were recorded at room temperature on a Fourier transform spectrophotometer (Biucker I.F.S. 110) with a resolution of 4 cm To compare the integrated adsorbances of the various samples the weight of the pellet and the Pd content were considered. The samples were placed in a heatable cell where the catalysts were treated "in situ". Different kinds of experiments were carried out ... 

The data from the Beckman spectrophotometer measiired at three different wavelengths, 280 and 350 nm are shown in Figures 5... 

The ultraviolet-visible spectrophotometer is the most widely used detector for HPLC. The basis of UV-VIS detection is the difference in the absorbance of light by the analyte and the solvent. A number of functional groups absorb... 

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... 

A modern spectrophotometer (UV/VIS, NIR, mid-IR) consists of a number of essential components source optical bench (mirror, filter, grating, Fourier transform, diode array, IRED, AOTF) sample holder detector (PDA, CCD) amplifier computer control. Important experimental parameters are the optical resolution (the minimum difference in wavelength that can be separated by the spectrometer) and the width of the light beam entering the spectrometer (the fixed entrance slit or fibre core). Modern echelle spectral analysers record simultaneously from UV to NIR. 

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