Abstract

Thermogravimetric analysis coupled to Fourier transform infrared spectroscopy (TG/FT-IR) is a very popular technique for rubbers characterization. It involves analyses of the base polymer and additives. Ethylene–propylene–diene (EPDM) rubbers are frequently investigated by TG/FT-IR; however, the focus has been the degradation temperature range of the polymer. In this study, unvulcanized and vulcanized EPDM rubber and its additives were investigated by TG/FT-IR, without solvent extraction, and in a wide temperature range. Initially, the additives were individually characterized. TG/FT-IR identified the characteristic groups of all the additives analyzed and distinguished them from each other. Afterwards, unvulcanized and vulcanized EPDM rubbers were investigated without prior extraction.TG/FT-IR detected absorptions due to the additives tetramethylthiuram monosulfide and 2-mercaptobenzothiazole. Both of these sulfur-containing additives were present in the EPDM formulation at concentrations of 0.7 phr (0.63 wt %). The TG/FT-IR technique had some limitations, because not all the additives in EPDM rubber were detected. Paraffin oil, stearic acid and 2,2,4-trimethyl-1,2-dihydroquinoline functional groups were not observed in either the unvulcanized or vulcanized EPDM. Nevertheless, in addition to the ability of this method to detect sulfur-containing groups, the lack of a pre-extraction reduces the time and effort required for additive analysis in rubbers.

Keywords:
EPDM; additives; characterization; TG/FT-IR; TMTM; MBT

1 Introduction

Additives are selected and incorporated into rubbers to provide specific properties. Useful rubbers can only be obtained by appropriate compounding. Some chemicals provide processing aid, extended shelf-life or improved long-term performance, others enhance polymer properties. As a result, rubbers are complex chemical materials, which are difficult to analyze^[11 Bart, J. C. J. (2005). Additives in polymers: industrial analysis and applications. Chichester: John Wiley & Sons.^]. Analytical techniques that enable the detection of additives are of great importance for industries, especially for those cases in which they are present in very low concentrations.

Typically, there are two approaches for additive analysis in rubbers: extraction with solvent prior to analysis or direct determination. Extraction procedures can be very complex, labor-intensive, and not always reproducible^[11 Bart, J. C. J. (2005). Additives in polymers: industrial analysis and applications. Chichester: John Wiley & Sons.

2 Crompton, R. (2007). Determination of additives in polymers and rubbers. United Kingdom: Rapra Technology.^-33 Buchberger, W., & Stiftinger, M. (2012). Analysis of polymer additives and impurities by liquid chromatography/mass spectrometry and capillary electrophoresis/mass spectrometry. Advances in Polymer Science, 248, 39-67. http://dx.doi.org/10.1007/12_2011_147.
http://dx.doi.org/10.1007/12_2011_147... ^]; thus, direct analysis is always preferred if it is feasible.

Among the techniques for direct determination, thermogravimetric analysis coupled with Fourier transform infrared spectroscopy (TG/FT-IR) is one of the most powerful methods to study the thermal degradation of polymers. This technique has the merit of identifying the evolved gases of a polymer at different degradation temperatures; thus, it allows a temperature selective analysis^[44 Cervantes-Uc, J. M., Cauich-Rodríguez, J. V., Vazquez-Torres, H., & Licea-Claveríe, A. (2006). TGA/FTIR study on thermal degradation of polymethacrylates containing carboxylic groups. Polymer Degradation & Stability, 91(12), 3312-3321. http://dx.doi.org/10.1016/j.polymdegradstab.2006.06.005.
http://dx.doi.org/10.1016/j.polymdegrads... ^].

Ethylene–propylene–diene copolymer (EPDM) is one of the most important rubbers, and has uses in diverse applications, even in the aerospace field. Its saturated backbone provides remarkable resistance to oxygen, ozone, and heat^[55 Choi, S., & Kim, Y. (2011). Formation of C7-species pyrolysis products from ethylene-propylene heterosequences of poly(ethylene-co-propylene). Analytical and Applied Pyrolysis, 92(2), 384-391. http://dx.doi.org/10.1016/j.jaap.2011.07.014.
http://dx.doi.org/10.1016/j.jaap.2011.07... ^]. Some recently published studies have been related to the TG/FT-IR analysis of additives in EPDM. Jiang et al.^[66 Jiang, Y., Zhang, X., He, J., Yu, L., & Yang, R. (2011). Effect of Polyphenylsilsesquioxane on the ablative and flame-retardation properties of Ethylene Propylene Diene Monomer (EPDM) composite. Polymer Degradation & Stability, 96(5), 949-954. http://dx.doi.org/10.1016/j.polymdegradstab.2011.01.034.
http://dx.doi.org/10.1016/j.polymdegrads... ^] used TG/FT-IR to evaluate the effect of polyphenylsilsesquioxane (PPSQ) on the release of volatile products in EPDM samples. The results indicated that PPSQ affects volatile products of EPDM and is detected in its formulation by TG/FT-IR. Çavdar et al.^[77 Çavdar, S., Özdemir, T., & Usanmaz, A. (2010). Comparative study on mechanical, thermal, viscoelastic and rheological properties of vulcanised EPDM rubber. Plastics.Rubber and Composites, 39(6), 277-282. http://dx.doi.org/10.1179/174328910X12647080902970.
http://dx.doi.org/10.1179/174328910X1264... ^] studied different vulcanizing agent contents by TG/FT-IR. They observed that increasing vulcanizing agent content decreased band intensities of CO and CO₂ and enhanced the thermal stability of EPDM rubber. Özdemir^[88 Özdemir, T. (2008). Gamma irradiation degradation/modification of 5-ethylidene 2-norbornene (ENB)-based ethylene propylene diene rubber (EPDM) depending on ENB content of EPDM and type/content of peroxides used in vulcanization. Radiation Physics and Chemistry, 77(6), 787-793. http://dx.doi.org/10.1016/j.radphyschem.2007.12.010.
http://dx.doi.org/10.1016/j.radphyschem.... ^] utilized TG/FT-IR to evaluate irradiated EPDM rubber vulcanized with two types of peroxides. The main absorptions of this irradiated rubber were attributed to aromatic C-H, methylene C-H, methyl ether C-H, methyl C-H, CO, and CO₂. However, none of the studies attempted to detect additives at degradation temperatures other than the EPDM polymer degradation temperature.

In a previous study^[99 Sanches, N. B., Cassu, S. N., Diniz, M. F., & Dutra, R. C. L. (2014). Characterization of additives typically employed in EPDM formulations by using FT-IR of gaseous pyrolyzates. Polímeros: Ciência e Tecnologia, 24(3), 269-275. http://dx.doi.org/10.4322/polimeros.2014.066.
http://dx.doi.org/10.4322/polimeros.2014... ^], we employed Fourier transform infrared spectroscopy of gaseous pyrolyzates (PY-G/FT-IR) for the detection of additives in EPDM rubber. The absorptions of additives were identified in unvulcanized and vulcanized EPDM samples without prior extraction with solvent. This technique was able to detect sulfur-containing additives at concentrations as low as 1.4 phr (1.26%). However, as the whole amount of the evolved gas from pyrolysis was trapped into a gas cell at once, a temperature selective analysis was not possible.

A temperature selective analysis can be performed using TG/FT-IR; moreover, this technique can cover a wide range of temperatures and provide information related to evolving products. Hence, this study is aimed at the detection of additives in EPDM rubber using TG/FT-IR without solvent extraction. Initially, each additive was individually characterized to identify its characteristic absorptions. Subsequently, unvulcanized and vulcanized EPDM samples were evaluated using raw EPDM rubber as a reference sample. The absorptions related to additives were identified by comparing the TG/FT-IR spectra of additives and EPDM samples.

2 Materials and Methods

2.1 Materials

Paraffin oil, stearic acid, 2,2,4-trimethyl-1,2-dihydroquinoline (TMQ), tetramethylthiuram monosulfide (TMTM), and 2-mercaptobenzothiazole (MBT) were provided by Zanaflex Borrachas Ltda, Brazil, and analyzed individually as received.

As a reference sample, commercial grade EPDM Keltan 21 containing the diene ENB (ethylidene norbornene) was purchased from DSM Elastômeros do Brasil Ltda, Brazil, and used as received.

Unvulcanized and vulcanized (terminology in accordance with the ASTM D1566-11^[1010 American Society for Testing and Materials (2011). ASTM D1566-11: Standard Terminology Relating to Rubber. West Conshohocken: ASTM.^]) samples were prepared using EPDM Keltan 21 and rubber-grade chemicals according to the composition listed in Table 1.

The molecular structures of the analyzed compounds prior to degradation are shown in Figure 1. MBT is represented by two different structures because this additive can be present in two tautomeric forms (Figures 1v and 1vi)^[1111 Nieuwenhuizen, P. J., Reedijk, J., Van Duin, M., & McGill, W. J. (1997). Thiuram-and dithiocarbamate-accelerated sulfur vulcanization from the chemist's perspective; methods, materials and mechanisms reviewed. Rubber Chemistry and Technology, 70(3), 368-429. http://dx.doi.org/10.5254/1.3538436.
http://dx.doi.org/10.5254/1.3538436...

12 Contini, G., Di Castro, V., Stranges, S., Richter, R., & Alagia, M. (2002). Gas-phase photoemission study of 2-Mercaptobenzothiazole. The Journal of Physical Chemistry A, 106(12), 2833-2837. http://dx.doi.org/10.1021/jp013423b.
http://dx.doi.org/10.1021/jp013423b... ^-1313 Wu, F.-L., Hussein, W. M., Ross, B. P., & McGeary, R. P. (2012). 2-Mercaptobenzothiazole and its Derivatives: Syntheses, Reactions and Applications. Current Organic Chemistry, 16(13), 1555-1580. http://dx.doi.org/10.2174/138527212800840964.
http://dx.doi.org/10.2174/13852721280084... ^]. Contini et al.^[1212 Contini, G., Di Castro, V., Stranges, S., Richter, R., & Alagia, M. (2002). Gas-phase photoemission study of 2-Mercaptobenzothiazole. The Journal of Physical Chemistry A, 106(12), 2833-2837. http://dx.doi.org/10.1021/jp013423b.
http://dx.doi.org/10.1021/jp013423b... ^] stated that MBT exists in the vapor phase only in its tautomeric thione (benzothiazoline-2-thione) form, which contains a C=S bond and a hydrogen bonded to the nitrogen, rather than the thiol form, which contains an endocyclic C=N bond and a hydrogen bonded to sulfur. According to Wu et al.^[1313 Wu, F.-L., Hussein, W. M., Ross, B. P., & McGeary, R. P. (2012). 2-Mercaptobenzothiazole and its Derivatives: Syntheses, Reactions and Applications. Current Organic Chemistry, 16(13), 1555-1580. http://dx.doi.org/10.2174/138527212800840964.
http://dx.doi.org/10.2174/13852721280084... ^] and Mohamed et al.^[1414 Mohamed, T. A., Mustafa, A. M., Zoghaib, W. M., Afifi, M. S., Farag, R. S., & Badr, Y. (2008). Reinvestigation of benzothiazoline-2-thione and 2-mercaptobenzothiazole tautomers: conformational stability, barriers to internal rotation and DFT calculations. Journal of Molecular Structure: THEOCHEM, 868(1-3), 27-36. http://dx.doi.org/10.1016/j.theochem.2008.07.037.
http://dx.doi.org/10.1016/j.theochem.200... ^], thione is the dominant form in the solid state. For a better understanding of the structural differences, the thione form of the MBT molecule is shown in Figure 1.

Figure 1
Molecular structure of the analyzed compounds prior to degradation (adapted from Sanches et al.^[99 Sanches, N. B., Cassu, S. N., Diniz, M. F., & Dutra, R. C. L. (2014). Characterization of additives typically employed in EPDM formulations by using FT-IR of gaseous pyrolyzates. Polímeros: Ciência e Tecnologia, 24(3), 269-275. http://dx.doi.org/10.4322/polimeros.2014.066.
http://dx.doi.org/10.4322/polimeros.2014... ^]).

2.2 TG/FT-IR analysis

TG/FT-IR analyses were performed using a PerkinElmer Pyris 1 TGA coupled with a PerkinElmer Spectrum One FT-IR. The transfer line and FT-IR gas cell were maintained at 210 and 230 °C, respectively. The spectra were collected at resolution of 8 cm⁻¹ with a co-add of 8 scans per spectrum, resulting in one spectrum collected every 22 s. Each sample (ca. 20 mg) was heated from room temperature to 900 °C under a nitrogen atmosphere.

Heating rate and gas flow are the experimental parameters that have the greatest effect on the results of a TG/FT-IR experiment^[1515 Berbenni, V., Marini, A., Bruni, G., & Zerlia, T. (1995). TG/FT-IR: an analysis of the conditions affecting the combined TG/Spectral response. Thermochimica Acta, 258, 125-133. http://dx.doi.org/10.1016/0040-6031(94)02237-I.
http://dx.doi.org/10.1016/0040-6031(94)0... ^]. Based on previous studies and recommendations of the manufacturer of the equipment, tests were performed to determine the optimal settings. Moreover, Gram–Schmidt reconstruction (GSR) profiles, which indicate the relative intensities of gases in the gas cell, were qualitatively compared. The optimal conditions, which maximized the FT-IR response, were determined to be the combination of a 20 °C/min heating rate with a 25 ml/min gas flow. According to Berbenni et al.^[1515 Berbenni, V., Marini, A., Bruni, G., & Zerlia, T. (1995). TG/FT-IR: an analysis of the conditions affecting the combined TG/Spectral response. Thermochimica Acta, 258, 125-133. http://dx.doi.org/10.1016/0040-6031(94)02237-I.
http://dx.doi.org/10.1016/0040-6031(94)0... ^], a well-adjusted TG/FT-IR experiment will present GSR and differential thermogravimetric (DTG) curves with similar profiles. In addition to providing the most intense absorptions, the selected parameters also showed excellent agreement between the GSR and DTG curves.

2.3 Selection of FT-IR spectra

In a typical TG/DTG result, the maximum value of the derivative curve indicates the maximum degradation rate. At this value, the quantity of evolving gases reaches its maximum. A single TG/DTG experiment can present one or multiple maxima depending on the sample components and its degradation characteristics.

An FT-IR spectrum was collected for each observed maximum degradation rate, which agreed with the maxima of the GSR profile with a delay of a few seconds. For some samples, a single spectrum was sufficient to represent the whole experiment, whereas for other samples, in which more than one degradation event was detected, more spectra were collected.

Moreover, the main absorptions determined in the spectra of additives were investigated in unvulcanized and vulcanized EPDM samples at the same temperature at which they appeared in the degradation of the additives.

In this study, all the FT-IR spectra were obtained from TG/FT-IR experiments, which are referred to as TG/FT-IR spectra.

3 Results and Discussion

3.1 Degradation temperatures

Initially, the additives, raw EPDM, and both unvulcanized and vulcanized EPDM were analyzed separately by TG/FT-IR. A set of TG/DTG curves, GSR curves, and FT-IR spectra was obtained for each sample.

Figure 2 shows the degradation temperatures obtained from the TG/DTG curves. A comparison between the degradation ranges of EPDM and its additives is useful because it indicates the temperature at which the characteristic absorptions of the additives should be searched for in the unvulcanized and vulcanized EPDM TG/FT-IR experiments.

Figure 2
Degradation temperature of components from TG/FT-IR experiments.

Figure 2 shows that only TMTM presents a narrow degradation temperature region of 180-310 °C, whereas the other additives show wide degradation regions. Raw EPDM degradation starts at approximately 250 °C; therefore, at lower temperatures, additive absorptions should be observed in unvulcanized and vulcanized EPDM without interference from characteristic EPDM bands. At higher temperatures, most additive absorptions should simultaneously be observed with the polymer bands.

The comparison between raw, unvulcanized and vulcanized EPDM confirm their peculiarities. Raw EPDM presents a more narrow temperature degradation range, as expected for a neat polymer. Unvulcanized and vulcanized EPDM degradation is broader because of the additive content. The comparison between unvulcanized and vulcanized EPDM shows that unvulcanized EPDM degradation begins at a lower temperature, although both contain the same formulation. Vulcanized EPDM was heated to approximately 150-180 °C in the crosslinking process; therefore, to some extent, it loses a certain quantity of low molecular weight additives.

3.2 TG/FT-IR analysis of additives

IR spectra of gaseous products can be very complex because they present a large number of absorptions. In this study, for peak assignment, the presence or absence of characteristic functional groups in the TG/FT-IR spectra was used. Figure 3 shows the FT-IR spectra of additives obtained from the TG/FT-IR technique.

Figure 3
TG/FT-IR spectra of (a) paraffin oil at 450 °C; (b) stearic acid at 324 °C; (c) TMQ at 362 °C; and (d) TMQ at 473 °C.

The main bands observed in the TG/FT-IR spectrum of paraffin oil (Figure 3a) are 3085, 3016, 2933, 2868, 1462, 1380, 949, and 911 cm⁻¹. The peaks at 3085 and 3016 cm⁻¹are assigned to the C-H group and/or C-H aromatic group, whereas those at 2933, 2868 and 1380 cm⁻¹ are assigned to the CH₃ group. The band at 1462 cm⁻¹ is assigned to C-H group. Although aromatic groups are not expected in the TG/FT-IR spectrum of paraffin oil, its presence can be explained by the fact that rubber-grade paraffin oils may contain 26%-40% of naphthenic oil and 2%-7% of aromatic oil^[1616 Loadman, M. J. R. (1998). Analysis of rubber and rubber-like polymers. Dordrecht: Klumer Academic Publishers.^].

The TG/FT-IR spectrum of stearic acid is shown in Figure 3b. The band at 3576 cm⁻¹ is assigned to the OH group. The peaks at 2933 and 2864 cm⁻¹ are assigned to the CH₂ groups. The absorption at 1776 cm⁻¹ is assigned to the C=O group. The bands at 1462 and 1126 cm⁻¹ are assigned to the CH₂ group, whereas the band at 1372 cm⁻¹ is assigned to the CH₃ group^[1717 Zhang, Z., Dallek, S., Vogt, R., Li, Y., Topping, T. D., Zhou, Y., Schoenung, J. M., & Lavernia, E. J. (2010). Degassing behavior of nanostructured al and its composites. Metallurgical and Materials Transactions. A, Physical Metallurgy and Materials Science, 41(2), 532-541. http://dx.doi.org/10.1007/s11661-009-0089-6.
http://dx.doi.org/10.1007/s11661-009-008... ^,1818 Jansen, J. A. J., Van Der Maas, J. H., & Boer, A. P. (1992). Hyphenated on-the-spot TG/FT-IR technique. Applied Spectroscopy, 46(1), 88-92. http://dx.doi.org/10.1366/0003702924444452.
http://dx.doi.org/10.1366/00037029244444... ^].

The TG/FT-IR spectra corresponding to TMQ degradation at 362 and 473 °C are shown in Figures 3c and 3d, respectively. The spectrum at 362 °C showed a band at 3015 cm⁻¹, which is assigned to the C-H or H-C=C group. The bands around 2968–2877 and 1059-1005 cm⁻¹ are assigned to the CH₃ group. The peaks at 1603 and 744 cm⁻¹ are assigned to the C-C aromatic and C-H groups, respectively. The absorption at 1304 cm⁻¹ is assigned to the N-H^[1919 Welti, D., & Stephany, R. (1968). Some comments on the infrared spectra of vapors. Applied Spectroscopy, 22(6), 678-688. http://dx.doi.org/10.1366/000370268774384119.
http://dx.doi.org/10.1366/00037026877438... ^] and/or C-N^[2020 Smith, A. L. (1979). Applied infrared spectroscopy.New York: John Wiley & Sons.^] groups, whereas the bands at 1263 and 1162 cm⁻¹ are assigned to the C-N aromatic group.

The spectrum at 473 °C showed the same bands as the one at 362 °C; however, other absorptions were detected, which are described as follows. The bands at 1497, 1380, and 835-812 cm⁻¹ are assigned to the C-C aromatic and/or CHN, CH₃, and C-H groups of the benzene ring, respectively^[2020 Smith, A. L. (1979). Applied infrared spectroscopy.New York: John Wiley & Sons.^]. These bands were possibly not detected at 362 °C because of the low amount of evolved gas at this temperature.

Figure 4a shows the TG/FT-IR spectrum of TMTM at 294 °C. The bands at 2941-2812 cm⁻¹ are assigned to the CH₃ group. The bands at 2072 and 2048 cm⁻¹ probably can be assigned to the N=C=S (isothiocyanate) group^[2121 Silverstein, R. M., Webster, F. X., & Kiemle, D. J. (2005). Spectrometric identification of organic compounds. New York: John Wiley & Sons.

22 Meyers, R. A. (2001). Encyclopedia of physical science and technology. Oxford: Elsevier.

23 Fiels, L. D., Sternhell, S., & Kalman, J. R. (2008). Organic structures from Spectra. Chichester: John Wiley & Sons.^-2424 Coates, J. (2000). Interpretation of infrared Spectra, a practical approach. In R. A. Meyers (Ed.), Encyclopedia of analytical chemistry (pp. 10815-10837). Chichester: John Wiley & Sons.^].

Figure 4
TG/FT-IR of (a) TMTM at 294 °C; (b) MBT at 361 °C; and (c) MBT at 784 °C.

The spectra of CS₂ in the gaseous state obtained from the reference databases^[2525 NIST Standard Reference Database WebBook2013Retrieved in 3 Mar. 2013, from http://webbook.nist.gov/cgi/cbook.cgi?ID=C75150&Units=SI&Type=IR-SPEC
http://webbook.nist.gov/cgi/cbook.cgi?ID... ^,2626 BIO-RAD/SADTLER Reference Database2013Retrieved in 3 Mar. 2013, from Retrieved from https://scifinder.cas.org/
https://scifinder.cas.org/... ^], show absorptions at approximately 2320, 2179, and 1530 cm⁻¹, which are in excellent agreement with the bands observed at 2336-2316, 2193-2179, and 1539-1524 cm⁻¹. Moreover, similar to other studies, a band located between 1523 and 1541 cm⁻¹can be attributed to the CS₂ group^[2727 Person, W. B., & Hall, L. C. (1964). Absolute infrared intensities of CS2 fundamentals in gas and liquid phases: an interpretation of the bond moments of CO and CS. 22Spectrochimica Acta, 20(5), 771-779. http://dx.doi.org/10.1016/0371-1951(64)80076-X.
http://dx.doi.org/10.1016/0371-1951(64)8... ^,2828 Hoffmann, F., Riesen, R., & Foreman, J. (2000). Characterization of thermal stability and reaction products by means of TGA-FTIR coupling. American Laboratory, 32(1), 13-17.^].

Therefore, considering the chemical structure of TMTM and the references in the literature, doublets can be attributed to the presence of the C=S and/or CS₂ group in the TMTM degradation products.

The TG/FT-IR spectra corresponding to MBT degradation at 361 and 784 °C are shown in Figures 4b and 4c, respectively. The spectrum at 361 °C has a band at 3748 cm⁻¹, which can be assigned to the N-H group. The peaks at 3076 and 755 cm⁻¹ are assigned to the aromatic C-H group. The band at 2895 cm⁻¹ is assigned to the CH₂ group. The doublet at 2071-2046 cm⁻¹ and the peak at 656 cm⁻¹ are assigned to the N=C=S group^[2020 Smith, A. L. (1979). Applied infrared spectroscopy.New York: John Wiley & Sons.^]. These absorptions are in excellent agreement with the benzothiazole spectrum in the literature^[2525 NIST Standard Reference Database WebBook2013Retrieved in 3 Mar. 2013, from http://webbook.nist.gov/cgi/cbook.cgi?ID=C75150&Units=SI&Type=IR-SPEC
http://webbook.nist.gov/cgi/cbook.cgi?ID... ^]. Doublets at 2193-2179 (very subtle) and 1539-1525 cm⁻¹ are assigned to the C=S and/or CS₂ group, which is analogous to the TMTM assignment. These assignments confirm the presence of the thione form in the vapor phase, as indicated by Contini et al.^[1212 Contini, G., Di Castro, V., Stranges, S., Richter, R., & Alagia, M. (2002). Gas-phase photoemission study of 2-Mercaptobenzothiazole. The Journal of Physical Chemistry A, 106(12), 2833-2837. http://dx.doi.org/10.1021/jp013423b.
http://dx.doi.org/10.1021/jp013423b... ^].

After 450 °C, the intensity of the bands observed in the 361 °C spectrum starts decreasing with the emergence of a doublet at 1376-1343 cm⁻¹, indicating the structural transformation of the molecule. The spectrum at 784 °C shows this doublet; however, it is inconclusive for determining the evolved products during MBT thermal degradation.

According to Brooks et al.^[2929 Brooks, C. T., Peacock, S. J., & Reuben, B. G. (1979). Pyrolysis of benzene. Journal of the Chemical Society, Faraday Transactions I, 75(0), 652-662. http://dx.doi.org/10.1039/f19797500652.
http://dx.doi.org/10.1039/f19797500652... ^], pyrolysis of pure benzene leads to ring opening at 763 °C, leading to the generation of methane as one of the degradation products. The spectrum of methane from the literature^[2525 NIST Standard Reference Database WebBook2013Retrieved in 3 Mar. 2013, from http://webbook.nist.gov/cgi/cbook.cgi?ID=C75150&Units=SI&Type=IR-SPEC
http://webbook.nist.gov/cgi/cbook.cgi?ID... ^] shows absorptions in the region of 1376-1343 cm⁻¹, indicating that they could be related to the CH₃ group. Nevertheless, recent studies have assigned these peaks to the C-C group of the benzene ring^[3030 Xiao-Hong, L., Zheng-Xin, T., & Xian-Zhou, Z. (2009). Molecular structure, IR spectra of 2- mercaptobenzothiazole and 2-mercaptobenzoxazole by density funcional theory and ab initio Hartree-Fock calculations. Spectrochimica Acta. Part A: Molecular and Biomolecular Spectroscopy, 74(1), 168-173. http://dx.doi.org/10.1016/j.saa.2009.05.026.
http://dx.doi.org/10.1016/j.saa.2009.05.... ^,3131 Sathyanarayanmoorthi, V., Karunathan, R., & Kannappan, V. (2013). Molecular modeling and spectroscopic studies of Benzothiazole. Journal of Chemistry, 2013, 1-14. http://dx.doi.org/10.1155/2013/258519.
http://dx.doi.org/10.1155/2013/258519... ^], or to the ring vibrations of the heterocyclic MBT ring^[2121 Silverstein, R. M., Webster, F. X., & Kiemle, D. J. (2005). Spectrometric identification of organic compounds. New York: John Wiley & Sons.^].

3.3 TG/FT-IR analysis of EPDM

TG/FT-IR results of raw, unvulcanized, and vulcanized EPDM can complement each other. In this study, raw rubber was analyzed as a reference sample, and its FT-IR spectrum was compared with the spectra of unvulcanized and vulcanized EPDM to differentiate the polymer absorptions. Unvulcanized rubber was analyzed by TG/FT-IR to obtain the spectrum before vulcanization, which is when additives are chemically preserved.

The TG/FT-IR spectra of the evolved products of raw, unvulcanized, and vulcanized EPDM are shown in Figure 5. Figure 5a shows the TG/FT-IR spectrum of raw EPDM. The peak at 3086 cm⁻¹ is assigned to the olefinic and/or aromatic C-H. The peaks at 988 and 911 cm⁻¹ are assigned to the vinylic C=C. The band around 949 cm⁻¹ is assigned to the trans C=C. The bands observed at 889 cm⁻¹ and at 1385 cm⁻¹ are assigned to the RR′CCH₂ and CH₃ groups, respectively^[2020 Smith, A. L. (1979). Applied infrared spectroscopy.New York: John Wiley & Sons.^]. The absorptions detected in the raw EPDM FT-IR spectrum can help evaluate additive-related absorptions in the formulated EPDM.

Figure 5
TG/FT-IR of (a) raw EPDM at 494 °C; (b) unvulcanized EPDM at 272 °C; (c) vulcanized EPDM at 280 °C; (d) unvulcanized EPDM at 509 °C; and (e) vulcanized.

TG/FT-IR spectra of unvulcanized and vulcanized EPDM (Figures 5b and 5c) are very similar at 272 and 280 °C, respectively. These spectra show very weak doublets around 2192-2179 and 2071-2047 cm⁻¹. A more intense doublet is detected in the region of 1540-1525 cm⁻¹. These peaks are absent in the spectrum of raw EPDM (Figure 5a); thus, they are related to the additives. Only TMTM and MBT TG/FT-IR spectra show similar bands; thus, it can be assumed that these absorptions are related to them.

Figures 5d and 5e show the TG/FT-IR spectra of unvulcanized and vulcanized EPDM at 509 and 517 °C, respectively. At these temperatures, unvulcanized and vulcanized EPDM degradation products show only polymer-related absorptions, which are in excellent agreement with the raw EPDM TG/FT-IR spectrum (Figure 5a).

TG/FT-IR results of raw EPDM, as well as the results for unvulcanized and vulcanized EPDM at 509 and 517 °C, respectively, exclusively show the EPDM polymer. Their assignments are in accordance with a published study^[3232 Choi, S., & Kim, Y. (2011). Analysis of 5-ethylidene-2-norbornene in ethylene-propylene-diene terpolymer using pyrolysis-GC/MS. Polymer Testing, 30(5), 509-514. http://dx.doi.org/10.1016/j.polymertesting.2011.04.005.
http://dx.doi.org/10.1016/j.polymertesti... ^] that evaluated EPDM rubber by coupling pyrolysis–gas chromatography and mass spectrometry (PY-GC/MS). Its results indicate a mix of alkanes and alkenes among the major products of EPDM thermal degradation.

Moreover, the main absorptions of paraffin oil, stearic acid, and TMQ were investigated in EPDM TG/FT-IR spectra at the temperature range, in which the additive degradation was observed. The TG/FT-IR spectra of unvulcanized and vulcanized EPDM show no peaks that could be related to these additives.

In a previous study^[99 Sanches, N. B., Cassu, S. N., Diniz, M. F., & Dutra, R. C. L. (2014). Characterization of additives typically employed in EPDM formulations by using FT-IR of gaseous pyrolyzates. Polímeros: Ciência e Tecnologia, 24(3), 269-275. http://dx.doi.org/10.4322/polimeros.2014.066.
http://dx.doi.org/10.4322/polimeros.2014... ^], a band at 771/772 cm⁻¹ from paraffin oil, stearic acid, and TMQ pyrolysis was detected in the PY-G/FT-IR spectra of unvulcanized and vulcanized EPDM. In the TG/FT-IR experiments, the absence can be explained by features of the technique. In this study, the evolved gases are carried to FT-IR by the flow gas, which dilutes the degradation products; moreover, the amount of sample is significantly less than the one analyzed with the PY-G/FT-IR technique.

Table 2 summarizes the functional groups assigned to the additives and EPDM by TG/FT-IR experiments, and relates them to the temperature at which spectra were collected. It can be seen that unvulcanized and vulcanized EPDM spectra were collected at a higher temperature than the raw EPDM spectrum. As the temperatures are related to the maximum degradation rate of the polymer, the differences are possibly due to the additives (unvulcanized and vulcanized EPDM) and the crosslinking effect (vulcanized EPDM only).

Some differences in absorption intensities are expected between the TG/FT-IR spectra of unvulcanized and vulcanized EPDM. Vulcanized gaseous output is expected to be lower in quantity with less intense absorptions because the crosslinking process involves temperatures around 150 °C, which can alter the additives and cause chemical reactions. Although this study involves only qualitative analysis, this quantitative aspect could prevent detection of additives. For example, sulfur compounds could be partially or totally consumed in the reticulation reaction; consequently, their bands might lose intensity or even disappear from the FT-IR spectra of vulcanized rubber. Nevertheless, in this study, the unvulcanized and vulcanized EPDM TG/FT-IR spectra are very similar.

Intriguingly, the TG/FT-IR technique was able to detect only the sulfur-containing additives TMTM and MBT in unvulcanized and vulcanized EPDM. Both additives demonstrated similar characteristic absorptions related to sulfur compounds in the regions of 2192-2179, 2071-2047, and 1540-1524 cm⁻¹. These results confirm that absorptions related to the sulfur compounds show stronger intensities in the gaseous state than in the solid and liquid state^[99 Sanches, N. B., Cassu, S. N., Diniz, M. F., & Dutra, R. C. L. (2014). Characterization of additives typically employed in EPDM formulations by using FT-IR of gaseous pyrolyzates. Polímeros: Ciência e Tecnologia, 24(3), 269-275. http://dx.doi.org/10.4322/polimeros.2014.066.
http://dx.doi.org/10.4322/polimeros.2014... ^]. TG/FT-IR was capable of detecting sulfur compounds in concentrations as low as 1.4 phr (1.26%), considering the sum of TMTM and MBT content in the compounds. This confirms the potential of this method to investigate these types of materials, even with a considerably smaller sample than that used in the PY-G/FT-IR technique^[99 Sanches, N. B., Cassu, S. N., Diniz, M. F., & Dutra, R. C. L. (2014). Characterization of additives typically employed in EPDM formulations by using FT-IR of gaseous pyrolyzates. Polímeros: Ciência e Tecnologia, 24(3), 269-275. http://dx.doi.org/10.4322/polimeros.2014.066.
http://dx.doi.org/10.4322/polimeros.2014... ^].

In our former study^[99 Sanches, N. B., Cassu, S. N., Diniz, M. F., & Dutra, R. C. L. (2014). Characterization of additives typically employed in EPDM formulations by using FT-IR of gaseous pyrolyzates. Polímeros: Ciência e Tecnologia, 24(3), 269-275. http://dx.doi.org/10.4322/polimeros.2014.066.
http://dx.doi.org/10.4322/polimeros.2014... ^], the PY-G/FT-IR technique was unable to differentiate TMTM and MBT from each other; however, TG/FT-IR could easily distinguish between them. This demonstrates the superiority of TG/FT-IR for analyzing sulfur additives. In fact, PY-G/FT-IR and TG/FT-IR can complement each other because the former has the advantage of providing a very concentrated evolved gas, which can be helpful in analyzing additives whose products present weak absorptions or are present in low concentrations in the rubber compound. On the other hand, TG/FT-IR has the disadvantage of yielding gases diluted with the flow gas, but is able to provide spectra at different temperatures and thus differentiate the components of complex degradation samples.

4 Conclusion

TG/FT-IR characterization of additives frequently used in EPDM rubber was performed. This technique was capable of distinguishing all the additives from each other without exception. By analyzing the degradation of these additives at different temperatures, TG/FT-IR demonstrated very distinct spectra. Furthermore, TMTM and MBT accelerators showed some similar characteristic absorptions, which are related to sulfur compounds. The presence of these specific absorptions enables the differentiation of additives with and without sulfur, by TG/FT-IR.

This technique was able to detect absorptions of sulfur additives in EPDM rubber at concentrations as low as 1.4 phr (1.26%), even in vulcanized EPDM. These specific absorptions were detected at temperatures lower than the temperatures at which the polymer bands were observed, in accordance to TMTM and MBT degradation characteristics. Moreover, the identification of functional groups of these additives was possible without their prior extraction using solvents in both unvulcanized and vulcanized EPDM.

Therefore, the TG/FT-IR technique can be employed for the analysis of separate additives, neat rubber (raw), and unvulcanized and vulcanized compounds. It demonstrated temperature selectivity, enabling the investigation of specific temperatures at which the additives degrade. Although the technique was unable to detect paraffin oil, stearic acid, and TMQ additives in unvulcanized and vulcanized EPDM, the sulfur-related characteristic absorptions of TMTM and MBT were identified.

5. References

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