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picture1_Method Time Measurement Pdf 89490 | Summary Of Tg And Dta


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File: Method Time Measurement Pdf 89490 | Summary Of Tg And Dta
differential thermal analysis dta thermogravimetric analysis tg thermal analysis is the analysis of a change in a property of a sample which is related to an imposed change in the ...

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                   Differential thermal analysis (DTA) / Thermogravimetric analysis (TG) 
                 Thermal analysis is the analysis of a change in a property of a sample, which is related to an 
                 imposed change in the temperature. The sample is usually in the solid state and the changes that 
                 occur on heating include melting, phase transition, sublimation, and decomposition. 
                 The analysis of the change in the mass of a sample on heating is known as Thermogravimetric 
                 analysis (TG). TG measures mass changes in a material as a function of temperature (or time) 
                 under a controlled atmosphere. Its principal uses include measurement of a material's thermal 
                 stability  and  composition.  TG is most useful for dehydration, decomposition, desorption, and 
                 oxidation processes.   
                 The most widely used thermal method of analysis is Differential thermal analysis (DTA). In DTA, 
                 the  temperature of a sample is compared with that of an inert reference material during a 
                 programmed change of temperature. The temperature should be the same until thermal event 
                 occurs, such as melting, decomposition or change in the crystal structure. In an endothermic 
                 event takes place within the sample, the temperature of the sample will lag behind that of the 
                 reference and a minimum will be observed on the curve. On the contrary, if an exothermal event 
                 takes  place,  then  the  temperature  of  the  sample  will  exceed  that  of  the  reference  and  a 
                 maximum will be observed on the curve. The area under the endotherm or oxotherm is related 
                 to the enthalpy of the thermal event, ΔH. 
                 For many problems, it is advantageous to use both DTA and TG, because the DTA events can then 
                 be classified into those which do or do not involve mass change. A good example is shown as 
                 following: 
                                      Fig.1 TG & DTA curves for Al (Si O )(OH)  
                                                            4 4 10   8
                 At the temperature range 500 to 700°C there is a change in mass occurred on the TG curve, which 
                 corresponds to dehydration of Al (Si O )(OH) , and this dehydration shows up on DTA curve as 
                                           4 4 10   8
                 an endotherm. At 950 to 980°C, a second DTA effects occurs but this effect not occurs on the TG 
                 curve,  because  this  event  corresponds  to  recrystallization  of  the  dehydrated  kaolin.  This 
                 recrystallization process is oxothermic. 
                  
                 TG-DTA modes can be used to determine the following:- 
                 •  Melting points 
                 •  Glass transition temperatures 
                 •  Cristallinity 
              •  Moisture/ volatile content 
              •  Thermal and oxidative stability 
              •  Purity 
              •  Transformation temperatures 
                Q&A:    1. What kind of reference materials is used in DTA 
              The ideal reference material is a substance with the same thermal mass as the sample, but with 
              no thermal events over the temperature range of interest. In DTA is usually used alumina (Al O ), 
                                                                       2 3
              carborundum(SiC) or magnesium oxide(MgO) powder as the reference material for the analysis 
              of inorganic compounds. 
                   2. What’s the difference between DSC and DTA 
              The difference between DTA and DSC is that, in DTA the temperature of the sample is monitored 
              with respect to a reference sample; in DSC the sample and the reference are maintained at the 
              same temperature throughout the procedure. 
                Reference: 
              D.F.  Shriver,  P.  W. Atkins, Shriver & Atkins’ Inorganic Chemistry, 4th edition, Oxford University 
              Press, Oxford 2006, pp. 189-190. 
              Anthony R. West, Basic Solid State Chemistry, 2nd Edition, Wiley, London, 2001, pp. 203-210.   
              http://tetra.simtech.a-star.edu.sg/afbsUpload/FactSheet/ICES/TA%20Analyzer.pdf 
               
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...Differential thermal analysis dta thermogravimetric tg is the of a change in property sample which related to an imposed temperature usually solid state and changes that occur on heating include melting phase transition sublimation decomposition mass known as measures material function or time under controlled atmosphere its principal uses measurement s stability composition most useful for dehydration desorption oxidation processes widely used method compared with inert reference during programmed should be same until event occurs such crystal structure endothermic takes place within will lag behind minimum observed curve contrary if exothermal then exceed maximum area endotherm oxotherm enthalpy h many problems it advantageous use both because events can classified into those do not involve good example shown following fig curves al si o oh at range c there occurred corresponds this shows up second effects but effect recrystallization dehydrated kaolin process oxothermic modes determ...

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