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Zinc oxalate dihydrate

C2H3CIO acetyl chloride 75-36-5 -112 85 1 4836 2 900 C2H4062n zinc oxalate dihydrate 122465-35-4 25.00 2.5600 1... [Pg.209]

Zinc oxalate dihydrate ZnC303-2H30 4266-07-6 189.468 wh powder 100 dec 2.66 0.0026 s dil acid... [Pg.750]

After calibration by means of PulseTA it is possible to properly quantify the MS spectra not only for one evolved gas but also for multicomponent mixtures. This is illustrated by comparing the results obtained with both spectroscopic methods for the decomposition of zinc oxalate dihydrate (gaseous products water, CO and CO2). These results clearly show the advantages and drawbacks of both MS and FTIR for qualitative and quantitative analysis of the gas phase. Due to fragmentation of the evolved CO2 the results obtmned by TA-MS (Figure 8) can not be used for unambiguous confirmation of CO formation without calibration of the mass spectrometric signals. [Pg.104]

Potassium perchlorate KCIO 1.05 10-3 Zinc oxalate dihydrate ZnCjO 2HjO 1.38 10- ... [Pg.1080]

Decomposition of model substances method The third method of calibration is by carrying out an experimental run using certain well studied model substances such as copper sulfate pentahydrate, calcium carbonate, calcium oxalate mono hydrate, potassium carbonate, sodium hydroxide, zinc oxalate dihydrate, and benzoic acid. These model substances show well resolved dehydration and decomposition temperatures over a wide temperature range. [Pg.352]

See other pages where Zinc oxalate dihydrate is mentioned: [Pg.253]    [Pg.1323]    [Pg.742]    [Pg.1279]    [Pg.1316]    [Pg.16]    [Pg.13]    [Pg.236]    [Pg.505]    [Pg.725]    [Pg.1210]    [Pg.797]    [Pg.1364]    [Pg.742]    [Pg.1277]   
See also in sourсe #XX -- [ Pg.104 ]



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Dihydrate)

Dihydrates

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