Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Calorimeter scanning

Fig. 1. Differential scanning calorimeter (dsc) curves of three grades of low melting syndiotactic 1,2-polybutadiene. A, 90% 1,2 = 71° C B, 92% 1,2 ... Fig. 1. Differential scanning calorimeter (dsc) curves of three grades of low melting syndiotactic 1,2-polybutadiene. A, 90% 1,2 = 71° C B, 92% 1,2 ...
In a testing context, it refers to the first detection of exothermic-activity on the thermogram. The differential scanning calorimeter (DSC) has a scan rate of I0°C/min, whereas the accelerating rate calorimeter (ARC) has a sensitivity of 0.02°C/min. Consequently, the temperature at which thermal activity is detected by the DSC can be as much as 50°C different from ARC data. [Pg.2312]

Endothermic peak temperature according to the differential scanning calorimeter method. (Speed of temperature rise 20 C/min.) he figures apply to 2-mm-thick sheet injection molded with cylinder temperature of 150°C and mold temperature 20 C. [Pg.180]

In a differential scanning calorimeter, a sample and reference material are heated in separate, but identical, metal heat sinks. The temperatures of the sample and reference material are kept the same by varying the power supplied to the two heaters. The output is the difference in power as a function of heat added. [Pg.360]

The output of a differential scanning calorimeter is a measure of the power (the rate of energy supply) supplied to the sample cell. The thermogram in the third illustration shows a peak that signals a phase change. The thermogram does not look much like a heating curve, but it contains all the necessary information and is easily transformed into the familiar shape. [Pg.360]

A thermogram from a differential scanning calorimeter. The peak indicates a phase change in the sample, and the difference in base line before and after the phase transition is due to the difference in heat capacities of the two phases. [Pg.360]

A number of other thermodynamic properties of adamantane and diamantane in different phases are reported by Kabo et al. [5]. They include (1) standard molar thermodynamic functions for adamantane in the ideal gas state as calculated by statistical thermodynamics methods and (2) temperature dependence of the heat capacities of adamantane in the condensed state between 340 and 600 K as measured by a scanning calorimeter and reported here in Fig. 8. According to this figure, liquid adamantane converts to a solid plastic with simple cubic crystal structure upon freezing. After further cooling it moves into another solid state, an fee crystalline phase. [Pg.214]

Figure 8. The temperature dependence of the heat capacity in the condensed state for adamantane [5] as measured by a scanning calorimeter. Tu, stands for temperature of transition from rigid crystal (fee) to plastic crystal (cubic) state of adamantane and Tfas stands for fusion temperature. Figure 8. The temperature dependence of the heat capacity in the condensed state for adamantane [5] as measured by a scanning calorimeter. Tu, stands for temperature of transition from rigid crystal (fee) to plastic crystal (cubic) state of adamantane and Tfas stands for fusion temperature.
Differential Scanning Calorimeter (DSC) thermograms were obtained on a Perkin Elmer DSC-2 run at 10°C per minutes. Dynamic Mechanical Thermal Analysis (DMTA) spectra were obtained on a Polymer Labs DMTA at a frequency of 1Hz with a temperature range from -150°C to +150°C at a scan rate of 5°C per minute. [Pg.88]

Thermal Analysis - Differential Scanning Calorimetry (DSC) and thermal gravimetric analysis (TGA) were used to characterize the thermal properties of the polymers synthesized. DSC analysis was performed on a Perkin-Elmer Differential Scanning Calorimeter, Model 2C with a thermal analysis data station. Thermal gravimetric analysis (TGA) was carried out on a DuPont thermal gravimeter, Model 951. From the DSC and TGA plots of poly (N-pheny 1-3,4-dimethylene-... [Pg.134]

Thermal Properties. The glass transition temperature (Tg) and the decomposition temperature (Td) were measured with a DuPont 910 Differential Scanning Calorimeter (DSC) calibrated with indium. The standard heating rate for all polymers was 10 °C/min. Thermogravimetric analysis (TGA) was performed on a DuPont 951 Thermogravimetric Analyzer at a heating rate of 20 °C/min. [Pg.157]

Chemical compatibility and U.S. EPA Method 9090 tests must be performed on the synthetics that will be used to construct FMLs. Unfortunately, there is usually a lag period between the time these tests are performed and the actual construction of a facility. It is very rare that at the time of the 9090 test, enough material is purchased to construct the liner. This means that the material used for testing is not typically from the same production lot as the synthetics installed in the field. The molecular structure of different polymers can be analyzed through differential scanning calorimeter... [Pg.1119]

Anonymous. Software for Oscillating Differential Scanning Calorimeter. Horsham, Seiko Instruments 1995. [Pg.620]

Safety studies of the graphite anode samples were performed using a Perkin-Elmer Differential Scanning Calorimeter (DSC, model Pyris 1) instrument. The temperature scanning rate was 10 C/min over a temperature range of 50 to 375°C. [Pg.301]

A DuPont 910 differential scanning calorimeter (DSC) and a DuPont 951 thermogravimetric analyzer (TGA) connected to a DuPont 1090 thermal analyzer 3ftre used to study the transition data, thermal stability, and char yield, respectively, for all the polymers. The DSC was run under a nitrogen stream at a flow rate of 80 c.c./min. and at a heating rate of 20°C/min.. [Pg.269]

The DSC curve of pseudoephedrine hydrochloride obtained with a Perkin Elmer DSC-1B differential scanning calorimeter is shown in Figure 5.7 The heating rate was 5°C/min. The heat of fusion is 6.4 Kcal/mol. The melting point (uncorrected) is 184°C. [Pg.496]

Adiabatic calorimeters are complex home-made instruments, and the measurements are time-consuming. Less accurate but easy to use commercial differential scanning calorimeters (DSCs) [18, 19] are a frequently used alternative. The method involves measurement of the temperature of both a sample and a reference sample and the differential emphasizes the difference between the sample and the reference. The two main types of DSC are heat flux and power-compensated instruments. In a heat flux DSC, as in the older differential thermal analyzers (DTA), the... [Pg.310]

ARC = Accelerating Rate Calorimeter (Columbia Scientific Instrument Corp.) DSC = Differential Scanning Calorimeter DTA = Differential Thermal Analysis RC1 = Reactor Calorimeter (Mettler-Toledo Inc.) RSST = Reactive System Screening Tool (Fauske and Associates) VSP = Vent Size Package (Fauske and Associates) ... [Pg.6]

Figure 2.6C shows the temperature difference between reference and sample as recorded by differential thermal analysis (DTA). Note also the similar differential scanning calorimeter (DSC) curve later in Figure 2.13. [Pg.21]

Differential scanning calorimeter measurement, 10 17-18. See also DSC thermogram... [Pg.268]

Silver behenate, differential scanning calorimeter data for, 19 339-340 Silver benzotriazole, 19 348, 362 as a photothermographic material, 19 333... [Pg.844]

Fig. 1. Differential Scanning Calorimeter (DSC). Ts=sample temperature, Tr=reference temperature, T0=oven temperature. Fig. 1. Differential Scanning Calorimeter (DSC). Ts=sample temperature, Tr=reference temperature, T0=oven temperature.
Glass transition temperatures of the uv-hardened films were measured with a Perkin Elmer Model DSC-4 differential scanning calorimeter (DSC) that was calibrated with an indium standard. The films were scraped from silicon substrates and placed in DSC sample pans. Temperature scans were run from -40 to 100-200 °C at a rate of 20 ° C/min and the temperature at the midpoint of the transition was assigned to Tg. [Pg.257]


See other pages where Calorimeter scanning is mentioned: [Pg.1916]    [Pg.313]    [Pg.338]    [Pg.97]    [Pg.177]    [Pg.529]    [Pg.124]    [Pg.511]    [Pg.655]    [Pg.650]    [Pg.298]    [Pg.780]    [Pg.395]    [Pg.47]    [Pg.103]    [Pg.183]    [Pg.142]    [Pg.123]    [Pg.278]    [Pg.276]    [Pg.198]    [Pg.19]    [Pg.53]    [Pg.293]    [Pg.846]    [Pg.306]    [Pg.365]   
See also in sourсe #XX -- [ Pg.117 ]

See also in sourсe #XX -- [ Pg.254 ]

See also in sourсe #XX -- [ Pg.3 , Pg.61 ]

See also in sourсe #XX -- [ Pg.76 , Pg.93 , Pg.145 , Pg.178 ]




SEARCH



Adiabatic scanning calorimeter

Calibration of differential scanning calorimeters

Calorimeter scanning, twin

Calorimeters

Differential scanning calorimeter

Differential scanning calorimeter 1294 INDEX

Differential scanning calorimeter Modulated

Differential scanning calorimeter Thermal analysis

Differential scanning calorimeter output

Differential scanning calorimeter trace

Differential scanning calorimeter, measurement

Differential scanning calorimeters DSCs)

Differential scanning calorimeters calibration

Differential scanning calorimeters compensation DSCs

Differential scanning calorimeters enthalpy calibration

Differential scanning calorimeters heat capacity calibration

Differential scanning calorimeters temperature calibration

Differential scanning calorimeters types

Experimental results differential scanning calorimeter

Heat flux DSCs Differential scanning calorimeters

Heat-flux differential scanning calorimeter

Measured differential scanning calorimeter

Modulation differential scanning calorimeter

Modulation differential scanning calorimeter MDSC)

Power compensation DSCs scanning calorimeters

Pressurized differential scanning calorimeter

Temperature calibration of differential scanning calorimeters

© 2024 chempedia.info