Indian Journal of Materials Science

Indian Journal of Materials Science / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 787306 | 5 pages | https://doi.org/10.1155/2014/787306

Kinetics of Thermolysis of Nickel(II) Perchlorate Complex with n-Propylamine

Academic Editor: J. Luo
Received25 Nov 2013
Accepted10 Jan 2014
Published19 Feb 2014

Abstract

Complex of nickel perchlorate with n-propylamine has been synthesised with molecular formula [Ni(n-pa)3(ClO4)(H2O)]ClO4. It has been characterised by elemental analysis, thermogravimetry, UV-VIS, and IR spectroscopic data. Thermal properties have been investigated by thermogravimetry (TG) in static air and by simultaneous thermogravimetry-derivative thermogravimetry-differential thermal analysis (TG-DTG-DTA) in flowing nitrogen atmosphere. Kinetics of thermolysis has been analysed applying model-fitting and model-free isoconversional method on isothermal TG data recorded at five different temperatures. To observe the response of complex towards fast heating, explosion delay time has been recorded at various temperatures and kinetics of explosion has been studied using these data.

1. Introduction

Metal perchlorates have strong oxidizing properties and amines are reducing in nature. Amines have strong e donation power due to presence of lone pair e on their nitrogen atom. These two oxidizing and reducing groups can be easily incorporated in a single molecule by reacting metal perchlorate with amine resulting in the formation of metal amine perchlorate coordination compounds. Any composition having strong oxidizing and reducing groups simultaneously in a molecule will exhibit the properties of high energetic materials. Thus, metal perchlorate amine complexes will exhibit the properties of energetic material and undergo autotransmitted decomposition reactions [13] when subjected to a stimuli (heat, friction, shock, wave, etc.). Owing to their energetic properties these types of complexes have found applications in explosives, pyrotechnics, and propellants. Such type of complexes has been proved to be a strong burning rate modifier for hydroxyl terminated polybutadiene-ammonium perchlorate (HTPB-AP) based propellants [4, 5]. In search of insensitive high energetic materials, a strong interest is being given by the researches on such type of complexes (having oxidizing and reducing group in one molecule) and they have been synthesized and their properties have been extensively investigated [514]. In the present paper, we report the preparation, characterisation, thermolysis, and explosion characterisation of nickel perchlorate complex with n-propyl amine, water, and as ligands. Kinetics of early thermolysis was also investigated by applying model-fitting and isoconversional method.

2. Experimental

2.1. Materials

Nickel carbonate, perchloric acid, n-propyl amine (sd.fine), ethanol (Changshu Yangyuan Chemical, China), petroleum ether (Merk), and all of AR grades were used as received.

2.2. Preparation

The complex was prepared via two-step procedure. In first step hexahydrate nickel perchlorate was obtained by reacting nickel carbonate with 60% perchloric acid followed by recrystallisation. In second step, ethanolic solution of nickel perchlorate and n-propyl amine was mixed together, stirred well at room temperature, and filtered out some obtained light green ppt. From the filtrate, after 2-3 days light green crystals of desired complex were obtained. The crystals were washed with alcohol and dried.

Caution. Perchlorates are explosives. They should be handled with care. However, I have not found any problem during all experimental procedures.

2.3. Characterisation

Characterisation of complex was done by elemental analysis (C, H, N; Thermo Finnigan Flash EA 1112 CHNS analyzer), infrared [1517] (Perkin Elmer FT-IR spectrometer), UV-VIS spectroscopy and thermogravimetry (Table 1).


IR Element %, Observed/calculated
(cm−1) Assignments

448M–NC22.4/22.1
627Ionic perchlorateN8.6/8.5
753C–H defH6.1/6.4
990C–N str. Ni12.95/13.27
1089Ionic perchlorate
1112Bidentate
1145
1395C–NH2
1503 N–H bend.
1570
2705 C–H str.
2994
3034 NH2 (Pri)
3434O–H (H2O)

2.4. Thermal Analysis
2.4.1. TG in Air

Thermogravimetry in static air with heating rate of 10°C/min (Figure 1) was recorded using an indigenously fabricated TG apparatus [18] (sample mass 20 mg).

2.4.2. Simultaneous TG-DTG-DTA

These traces were obtained in flowing nitrogen atmosphere (100 mL/min), sample was ~2.5 mg at a heating rate of 10°C/min (Figure 2, Table 2).


StepTGDTA
Temperature range (°C)% decompositionPeak position (°C)Nature of peaks

I92–1214169Endo
II121–28812
III290–30570299Exo

2.4.3. Isothermal TG

Isothermal TG (Figure 3) was recorded in static air atmosphere using the same indigenously fabricated TG apparatus as mentioned earlier at five different temperatures (200, 210, 220, 230, and 240°C). Sample mass taken was 10 mg and readings were recorded for 30% decomposition.

2.4.4. Kinetic Analysis

Kinetics of decomposition has been investigated using isothermal TG data using model fitting (Table 3) [19] and isoconversional method [20, 21]. Variation of activation energy with extent of conversion is shown in Figure 4.


Serial numberModel Slope /kJmole−1 Mean deviationStandard deviation

1Power law3/41.13822128.217.70.97022.7282.877
2Power law2/31.21431978.116.40.96412.6132.756
3Power law1/20.61302148.717.80.97142.4862.628
4Power law−1/20.06052207.118.30.97402.2692.384
5Power law−1−0.00512224.618.50.97422.2542.378
6Mampel −1.10532275.118.90.96101.7551.853
7a-e3/40.72412177.118.10.97482.5702.711
8a-e2/3−0.02752249.818.70.95992.2682.390
9a-e1/2−0.41442260.218.80.96052.0852.201
10cs0.22402249.118.70.96862.3932.525
11T-d-diff0.26292305.119.10.96142.4702.605
12cc0.18692223.418.50.97132.3492.478
13P-T−1.63002237.518.60.95921.4541.536
14G-B1.20402256.118.70.96982.8913.049

2.4.5. Explosion Delay Experiments

This experiment was performed using tube furnace technique [22] (sample mass 10 mg) at temperatures of 280, 300, 320, 340, and 360°C within experimental limit of ±1°C (Table 4). data were fitted in Arrhenius equation where is the Arrhenius factor, is the activation energy for explosion, is absolute temperature, and is the gas constant. A plot of versus is presented in Figure 5.


   at temperature (°C) (kJmol−1)

1239383585430.90.9842−1.915

3. Results and Discussion

Table 1 containing elemental analysis and IR data shows a good agreement between observed and calculated percentages of C, H, N, and Ni. The FT-IR spectra of the complex revealed bands at 448 cm−1 assigned to (M–N), 627 and 1089 cm−1 assigned to ionic perchlorate, and 1112 and 1145 cm−1 assigned to bidentate perchlorate ion ( symmetry) [22]. A broad peak at 3434 cm−1 is due to (O–H) of coordinated water. Other peaks are according to standard text. In the UV-VIS spectrum, the absorption maxima at 263 nm is due to transition and a peak at 378 nm is assigned for overlapping with charge transfer band. A band at 870 nm is assigned for transition. Thus, as suggested by the overall evidence given above, the complex can be formulated as [Ni(n-pa)3(ClO4)(H2O)]ClO4 in which Ni2+ is hexacoordinated. Out of six coordination sites, three sites are satisfied with nitrogen atoms; one from each n-propylamine and three sites with O-atoms; one from water molecule and two from one of the perchlorate ions acting as a bidentate ligand ( symmetry).

A perusal of TG curve recorded in static air with linear temperature increase shows that the complex decomposes in three steps. The very first step (92–121°C) is gradual in which coordinated H2O leaves the complex (~4% wt. Loss). In the second step (121–288°C) one of the n-propylamines is released (~12% wt. Loss). In the third step (290–305°C) the remaining residue [Ni(n-pa)2(ClO4)]ClO4 (might be tetracoordinated complex of Ni2+) ignites with smoke and low noise giving a sharp weight loss (~70%). At lost ~15% mass is left which corresponds to NiO (calculated mass 15.27%). In flowing N2 atmosphere (Figure 2) the decomposition pattern of complex is similar to static air. A DTG peak has been obtained corresponding to third step sudden weight loss. DTG were not obtained for first step because this step is very gradual. DTG peak for second step might be incorporated in third step of DTG peak. In DTA curve an endotherm at 169°C and this is to be in harmony with second step (removal of one of the n-pa molecule). A strong exothermic peak at 299°C has been received which suits the ignition of partially decomposed residue in the third step.

Thus, in the light of the above discussion, the thermolysis pattern of the complex can be given as In the order to calculate activation energy () for the removal of ligands (30% wt. Loss which includes H2O and 2 n-pa molecule), a set of reaction models (Table 3) [19] was used on isothermal TG data in the temperature range 200–240°C (Figure 3). values obtained (~18 kJ mole−1) are almost equal irrespective of the reaction model used.

Kinetic analysis of isothermal TG data applying isoconversional method [20, 21] concerns with the calculation of activation energy independent of the model but corresponding to the extent of conversion () of the complex. Figure 4 shows that at different values of , values in are different. Model-free isoconversional method is a better approach to obtain reliable and consistent kinetic data as compared to model-fitting methods.

The complex when subjected to sudden high temperature explodes with noise. To determine the activation energy of explosion () explosion delay time has been recorded at five different temperatures (Table 4). Activation energy for explosion was found to be 30.9 kJ mol−1. A graph of versus (Figure 5) shows that explosion delay time exponentially depends on temperatures.

4. Conclusion

The complex has been prepared and characterised by various techniques. TG-DTA study reveals that the complex decompose in three steps. After an initial weight loss (~16%) oxidiser () and fuel (reducing group i.e., n-pa) lead to ignition giving a sharp exothermic peak in DTA. End product of thermolysis corresponds to NiO. Complex explodes when kept suddenly under high temperatures.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors thank the Secretary Board of Management, Principal and Head of Department of Chemistry, DBS College, Kanpur, for providing laboratory facilities, and University Grants Commission, New Delhi, for financial assistance. Thanks are also due to Sophisticated Test and Instrumentation Centre, Cochin University of Science and Technology, for CHN, FT-IR, UV-VIS, and TG-DTA analyses.

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Copyright © 2014 Chandra Prakash Singh and Abhishek Singh. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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