Evaluation of the synergistic effect of layered double hydroxides with micro- and nano-CaCO 3 on the thermal stability of polyvinyl chloride composites

Abstract

Synergistic stabilizing effect of layered double hydroxides (LDHs) with micro- as well as nano-sized calcium carbonate (CaCO₃) on thermal stability of polyvinyl chloride (PVC) was studied and evaluated. Nano-sized CaCO₃ was prepared in the laboratory by matrix-mediated growth and controlled (in situ deposition) technique. Crystal size of nano-CaCO₃ was estimated by studying x-ray diffraction pattern. The PVC composites were prepared using Brabender Plastograph instrument. Various formulations were prepared by taking fixed amount of LDH and varying the concentration of micro-/nano-sized CaCO₃. PVC sheets of 1 mm thickness were prepared on compression molding machine. Thermal stability in terms of thermal degradation was studied by thermogravimetric analyzer. Surface morphology and mechanical property were studied using scanning electron microscopy and universal tensile machine. Increase in the onset temperature of the PVC sheets was considered as imparting a better thermal stability to PVC. Better synergistic effect on the stabilization of PVC was observed in case of LDH with nano-sized CaCO₃ and compared with micro-sized CaCO₃ _.

Keywords

Polyvinyl chloride layered double hydroxides thermal stability stabilizers

Introduction

Concept of nanocomposites of polymer deals with the effect of nano-sized fillers on the properties of composites. In contrast to the conventional systems where reinforcement is of the order of microns, discrete constituents of the order of a few nanometers represent polymer nanocomposites.¹ Uniform dispersion of these nano-sized filler particles produces ultra-large interfacial area per unit volume between nanofiller and a polymer matrix. Immense internal interfacial area and the nanoscopic dimensions fundamentally differentiate polymer nanocomposites from traditional composites and filled thermoplastics. These new materials improve the performance of classic materials by acquiring new modified properties, resulting in favorable cases of unique synergism between the polymer materials.^2,3

Polyvinyl chloride (PVC) is one of the most versatile polymers used in many field of applications. However, low thermal stability during the processing of PVC is a major concern and leads to PVC degradation. During PVC processing, thermal degradation occurs due to dehydrochlorination which develops conjugated double bonds in the PVC backbone.^4,5 This degradation is responsible for the sudden change in the PVC color and deterioration of mechanical properties. To overcome the problem of thermal stability of PVC, various heat stabilizers are being used. Among the stabilizers, lead based, organotin compounds and mixed metal soaps constitute the majority.

Extensive research has been carried out to use the nontoxic heat stabilizers for PVC. One of its kinds is layered double hydroxides (LDHs). LDH is an inorganic compound having HCl-scavenging ability to improve the thermal stability of PVC.⁶ Lin and coworkers reported that optimum level of LDH is 1–2 phr at which substantial improvement in thermal stability of PVC can be observed.⁷ Zhu and coworkers studied the effect of calcium carbonate (CaCO₃)/lithium chloride (Li₂CO₃) on the degradation behavior of PVC and their effect on HCl-scavenging ability.⁸ Literatures also have reports that various fillers like silica, clay, CaCO₃ and metal hydroxides or oxides may enhance the properties of polymers including PVC.⁹ Some of these fillers, like CaCO₃ and metal hydroxides or oxides, act as HCl scavenger. Mechanism for scavenging HCl involves reactions of fillers with HCl liberated from PVC, which results in the unavailability of HCl for autocatalytic dehydrochlorination. Therefore, there is decrease in the rate of further thermal degradation of PVC. HCl-scavenging effect of particulate fillers such as red mud, calcium carbonate (CaCO₃) and dolomite on the thermal degradation of PVC was investigated by thermogravimetric/mass spectrometry.¹⁰ Also Stephanie and coworkers investigated the synergistic effect of CaCO₃ and poly(vinyl butyral) on the thermal stability of PVC.¹¹ Gupta reported the synergistic effect of hydrotalcite and diketones with metal stearates on the thermal stabilization of PVC with improved thermal stability of the PVC.¹² However, the synergistic effect of CaCO₃ and LDH on the thermal stability of PVC has not been studied so far.

Hence in the present investigation we studied the synergistic effect of LDHs with micro- as well as nano-sized CaCO₃ on the thermal stabilization of PVC. In this work, we compounded the samples with the help of Brabender Plastograph machine, using LDHs and CaCO₃ in various proportions. Finally, the PVC sheets were prepared on compression molding machine, and the thermal stability of PVC composites was studied by thermogravimetric analysis (TGA). Morphology and mechanical property were studied to investigate the dispersion of fillers in the polymer matrix and reinforcement of matrix by the filler, respectively.

Experiment

Materials

A suspension-grade PVC (Reon grade–67) was obtained from the Reliance Industries Ltd., India. Calcium stearate, processing aid and stearic acid were kindly given by the Aryavarat Chemicals Ltd (Jalgaon, Maharashtra, India). All analytical grade chemicals and solvents such as glutaric acid, zinc oxide and toluene were used as obtained from S D Fine Chemicals (Mumbai, India). Other chemicals such as calcium chloride, potassium carbonate and polyethylene glycol (PEG; molecular weight 6000) were procured from the Qualigens India Ltd (Mumbai, India).

Synthesis of zinc glutarate

Zinc glutarate was synthesized from zinc oxide and glutaric acid.¹³ The powdered zinc glutarate was dried in a vacuum at 100°C for 24 h. Yield of zinc glutarate prepared in the laboratory was 99.8%.

Synthesis of nano-sized CaCO₃

Solution of calcium chloride (111 g, 1 M) was prepared by dissolving it in distilled water (100 mL). The PEG solution (372 g, 0.062 M) was prepared by dissolving it in hot distilled water (100 mL). These two solutions were mixed properly and digested gently for 12 h. Third solution, that is, potassium carbonate (106 g, 1 M) dissolved in distilled water (100 mL) was then added slowly to the above mixture under constant stirring. The newly formed particles of CaCO₃ were allowed to digest overnight. Nanoparticles were filtered, washed thoroughly with distilled water until the particles were freed of PEG traces and then dried at 110°C for 2 h. CaCO₃ filler was heated at about 250°C for removing traces of moisture before compounding.^14

–18

Preparation of the PVC/CaCO₃ nanocomposites

Different PVC formulations were prepared by varying concentrations of nano-sized CaCO₃ (1, 3 and 5 phr), keeping the LDH amount constant (2 phr). At the same time, commercial CaCO₃ PVC composites were also prepared for comparison of their performance with nano composites of PVC. All PVC formulations contain Ca stearate/Zn glutarate as primary stabilizer, plasticizer and lubricant. These formulations were dry blended in a mixer for 6–7 min. Then the dry blended PVC formulations were processed in a Brabender Plastograph internal mixer (GmbH & Co. KG, Duisburg, Germany) at 160°C for 5 min and at a mixing speed of 45 r/min. Successively, the PVC composites obtained were compression molded on heated compression molding machine at 170°C for 10 min. PVC sheets of 1 mm thickness were obtained, which were used for further analysis.

Characterization

X-Ray diffraction and transmission electron microscopy (TEM)

The particle size of the synthesized nano-sized CaCO₃ particles was determined using x-ray diffractometer (model: Xpert MPD; Philips, Holland) in the range of 0–1000 cps and diffraction angle of 0°–40° in sovitzkey Golay’s mode. Later, the size and morphology of the prepared nano fillers were confirmed using TEM (Philips Tecnai-20) at an accelerating voltage of 200 kV. The sample of synthesized fillers was dispersed in acetone in an ultrasonic bath for sufficient time before the analysis of particle size using the particles disperser on a C-coated grid

Thermogravimetric analysis

Thermal degradation behavior of the PVC samples was studied using Shimadzu thermogravimetric analyzer (TGA 50, Japan). Temperature programming was done from room temperature to 600°C at a heating rate of 20°C/min.

Scanning electron microscopy

Extent of dispersion of fillers and surface morphology of the PVC composites were inspected with scanning electron microscope (SEM JEOL JSM-6360A, Japan). Prior to analysis, the PVC samples were coated with platinum under vacuum.

Mechanical testing

Tensile strength of PVC sheets was measured using a universal tensile testing machine (Polyplast, Mumbai, India), according to ASTM D 638. The crosshead speed for testing was 50 mm/min, and all measurements were performed five times to obtain the average.

Results and discussion

Particle size determination

Particle size of synthesized nano-sized CaCO₃ was determined using x-ray diffraction pattern as shown in Figure 1, using the Scherer’s formula.

Figure 1.

XRD of nano-CaCO₃. CaCO₃: calcium carbonate; XRD: x-ray diffraction.

P a r t i c l e s i z e, d (Å) = k \cdot λ / Δ 2 θ C o s θ

where k = order of reflection, λ = 1.542, θ = diffraction angle and Δ2θ = full width at half maximum.

In the current study, the size obtained for synthesized CaCO₃ work was found to be in 44–66 nm range, which was later confirmed by TEM.

Particle size of synthesized CaCO₃ nanoparticles confirmed from TEM

In the present work, the particle size of the synthesized CaCO₃ filler was found to be in the range of 40–70 nm as verified using TEM micrograph (Figure 2).

Figure 2.

Transmission electron microscopy micrograph of calcium carbonate nanoparticles prepared by in situ deposition technique.

Thermal stability of PVC

TGA was used to investigate the thermal stability of PVC. The typical TGA curves of representative PVC samples are shown in Figure 3. It is reported in the literature that PVC degradation undergoes a two-step process.¹⁹ The first step involves dehydrochlorination of PVC around 200°C–350°C. The second step (350°C–550°C) mainly involves the breaking of the backbone chain of PVC due to the loss or pyrolysis to low-molecular-weight fragments produced by the decomposition of PVC.

Figure 3.

TGA thermograms of PVC samples (a) PVC without synergists (b) with 2 phr LDH (c) with 2 phr LDH + 3 phr micro-CaCO₃ (d) 2 phr LDH + 3 phr nano-CaCO₃. TGA: thermogravimetric analysis; PVC: polyvinyl chloride; LDH: layered double hydroxide; CaCO₃: calcium carbonate.

The data obtained from the TGA are shown in Table 1 and represented in Figure 4. The results show that the thermal stability of PVC is improved in all the case, that is, with the addition of LDH only in combination with micro-sized and nano-sized CaCO₃ in the PVC stabilizer system. Addition of only LDH along with the conventional Ca/Zn stabilizer system increases the onset temperature, while use of micro- as well as nano-sized CaCO₃ along with LDH further improves the thermal stability of PVC in terms of increased onset temperature. However, slight increase in the inflection temperature (T _max) was observed. Better thermal stability is thus observed when the PVC was added with 2 phr LDH in association with 3 and 5 phr nano-sized CaCO₃. As compared to the micro-sized CaCO₃ in the stabilizer system, nano-sized CaCO₃ show better results for the thermal stability of PVC. This may be attributed to more surface area available for nano-size CaCO₃ to interact with liberated HCl during PVC degradation as compared to interactions with micron size CaCO₃.²⁰ This indicates that the thermal stability of PVC improves by LDH which further enhanced synergistically by the addition of CaCO₃. These results could be explained by noting that calcium ions present in the nanoparticles are properly dispersed in a PVC matrix, scavenged the liberated HCl during the PVC degradation and subsequently formed calcium chloride.²¹ Along with this, the ion exchange mechanism of LDH with the release of HCl from PVC prevents further autocatalytic dehydrochlorination process, which in turn results in better thermal stability of PVC achieved by scavenging the liberated HCl.^5,6 This clearly points out that there is a synergism between LDH and nano-sized CaCO₃. The mechanism of reaction may be written as follow^11,22

Figure 4.

Onset temperatue of PVC samples without and with synergists: (1) PVC without synergists, (2) PVC with 2 phr LDH, (3) PVC with 2 phr LDH + 1 phr micro- and nano-CaCO₃, (4) PVC with 2 phr LDH + 3 phr micro- and nano-CaCO₃ and (5) PVC with 2 phr LDH + 5 phr micro- and nano-CaCO₃. PVC: polyvinyl chloride; LDH: layered double hydroxide; CaCO₃: calcium carbonate.

Table 1.

TGA results of the PVC sheets.

Sample	Content	T _onset (°C)	T _max (°C)
1	PVC without synergists	254	286
2	PVC with LDH (2 phr)	256	288
3	PVC with LDH + micro-CaCO₃ (1 phr)	257	288
3	PVC with LDH + nano-CaCO₃ (1 phr)	258	289
4	PVC with LDH + micro-CaCO₃ (3 phr)	259	289
4	PVC with LDH + nano-CaCO₃ (3 phr)	261	291
5	PVC with LDH + micro-CaCO₃ (5 phr)	260	290
5	PVC with LDH + nano-CaCO₃ (5 phr)	263	292

TGA: thermogravimetric analysis; PVC: polyvinyl chloride; LDH: layered double hydroxide; CaCO₃: calcium carbonate.

Morphological study

Figure 5 depicts the representative SEM micrographs of the surface morphology of the PVC sheets containing 3 phr of micro- and nano-sized CaCO₃. The SEM micrographs show that the micron size CaCO₃ filler (Figure 5) are not dispersed properly in a PVC matrix and formed bigger agglomerates than that of its nano-size CaCO₃. Incorporation of filler in Brabender Plastograph EC imparts sufficient dispersion in both micro- and nano-sized CaCO₃. Proper dispersion gives maximum interfacial area for nano-sized CaCO₃ to scavenge the liberated HCl during the high-temperature processing of PVC. Therefore, it prevents the autocatalytic action of HCl, which stops and prevents further dehydrochlorination of PVC. Thus, we conclude that the proper dispersion of nano-sized CaCO₃ provides better HCl-scavenging properties than the micron-sized one CaCO₃.

Figure 5.

SEM of PVC sheets having 3 phr of (a) micro-CaCO₃ and (b) nano-sized CaCO₃. PVC: polyvinyl chloride; CaCO₃: calcium carbonate; SEM: scanning electron microscopy.

Mechanical testing

The effects of commercial and nano-CaCO₃ with LDH on the tensile strength of PVC sheets are shown in Figure 6, and the corresponding data are given in Table 2. From the figure it was observed that the initial tensile strength of the PVC composites does not changed substantially but increased further with the addition of micro as well as nano-CaCO₃ along with LDH into the PVC stabilizer system. By the addition of 1, 3 and 5 phr CaCO₃ with LDH in PVC, the tensile strengths of the nano-CaCO₃–filled PVC composites were found to be much better than those of the micro-CaCO₃–filled PVC composites. The most substantial increase in the tensile strength value was observed at 3 and 5 phr of nano-CaCO₃. This is because the size of nano-CaCO₃ is much smaller and through their higher surface area can have better interactions with PVC matrix than those of micro-CaCO₃. This provides better interfacial interaction between matrix-filler surface, which results in the improvement of the mechanical strength of the polymer matrix.²³

Figure 6.

Tensile Strength of PVC samples without and with synergists: (1) PVC without synergists, (2) PVC with 2 phr LDH, (3) PVC with 2 phr LDH + 1 phr micro- and nano-CaCO₃, (4) PVC with 2 phr LDH + 3 phr micro- and nano-CaCO₃ and (5) PVC with 2 phr LDH + 5 phr micro- and nano-CaCO₃. PVC: polyvinyl chloride; LDH: layered double hydroxide; CaCO₃: calcium carbonate.

Table 2.

Mechanical testing results of the PVC sheets.

Sample	Content	Tensile strength (kg/cm²)
1	PVC without synergists	2.17
2	PVC with LDH (2 phr)	2.19
3	PVC with LDH + micro-CaCO₃ (1 phr)	2.23
3	PVC with LDH + nano-CaCO₃ (1 phr)	2.34
4	PVC with LDH + micro-CaCO₃ (3 phr)	2.32
4	PVC with LDH + nano-CaCO₃ (3 phr)	2.50
5	PVC with LDH + micro-CaCO₃ (5 phr)	2.57
5	PVC with LDH + nano-CaCO₃ (5 phr)	3.04

PVC: polyvinyl chloride; LDH: layered double hydroxide; CaCO₃: calcium carbonate.

Conclusion

Nano-sized CaCO₃ was prepared in the laboratory and its particle size was found to be in the range of 40–70 nm. We prepared different PVC composites with varying content of micro- and nano-sized CaCO₃, by keeping the LDH amount constant. Thermal stability of PVC sheets were studied by TGA. Addition of nano-sized CaCO₃ increases the onset temperature of PVC more substantially than that of micro-CaCO_3. Larger surface area provided by nano-sized CaCO₃ and better scavenging reaction of HCl resulted in enhanced thermal stability of PVC and better tensile strength than the micro-sized CaCO₃-filled PVC. Better synergism was observed in LDH with nano-sized CaCO₃ stabilizing system on the thermal stability of PVC compared to the synergistic effect of LDHs with micro-sized CaCO₃.

Footnotes

Acknowledgement

The authors thank the Aryavarat Chemical Limited, Jalgaon, India, for providing additives.

Funding

This work was supported by the University Grant Commission (UGC), New Delhi, India.

References

Gianellis

. Polymer layered silicate nanocomposites. Adv Mater 1996; 8(1): 29–35.

LeBaron

Wang

Pinnavaia

. Polymer-layered silicate nanocomposites: an overview. Appl Clay Sci 1999; 15(1-2): 11–29.

Krishnamoorthi

Vaia

Gianellis

. Structure and dynamics of polymer-layered silicate nanocomposites. Chem Mater 1996; 8(8): 1728–1734.

Benaniba

Belhaneche-Bensemra

Gelbard

. Stabilization of PVC by epoxidized sunflower oil in the presence of zinc and calcium stearates. Polym Degrad Stabil 2003; 82(2): 245–249.

Benavides

Edge

Allen

Tellez

. Polyene formation in poly(vinyl Chloride) stabilized with pre-heated metal stearates. Polym Bull 1999; 42(3): 273–279.

Van der Ven

Van Gemert

MLM

Batenburg

Keern

Gielgens

Koster

TPM

. On the action of hydrotalcite-like clay materials as stabilizers in polyvinyl chloride. Appl Clay Sci 2000; 17(1): 25–34.

Lin

Evans

Duan

. Modulating effect of Mg–Al–CO₃ layered double hydroxides on the thermal stability of PVC resin. Polym Degrad Stabil 2005; 88(2): 286–293.

Zhu

Zhang

. Effect of CaCO₃/LiCO₃ on the HCI generation of PVC during combustion. Polym Test 2003; 22(5): 539–543.

Xiong

Guo

. The kinetic studies of elimination of HCI during thermal decomposition of PVC in the presence of transition metal oxides. Polym Plastic Tech Eng 2005; 44: 275–288.

10.

Tamer

Jale

Mithat

Mehmet

Cornelia

Henning

. The effect of some fillers on PVC degradation. J Anal Appl Pyrol 2006; 75: 112–119.

11.

Stephanie

Claude

David

Albert

Cédric

. Synergetic effect of poly(vinyl butyral) and calcium carbonate on thermal stability of poly(vinyl chloride) nanocomposites investigated by TG–FTIR–MS. J Therm Anal Calorim 2010; 100: 667–677.

12.

Gupta

Agarwal

Banerjee

. Synergistic combination of metal stearates and β-diketones with hydrotalcites in poly(vinylchloride) stabilization. J Appl Polym Sci 2009; 112: 1056–1062.

13.

Yan-Bin

Liu

Wei-Qu

Liu

Meng-Hua

Hou

. Metal dicarboxylates as thermal stabilizers for PVC. Polym Degrad Stabil 2007; 92(8): 1565–1571.

14.

Saujanya

Radhakrishnan

. Structure development and crystallization behaviour of PP/nanoparticulate composite. Polymer 2001; 42(16): 6723–6731.

15.

Saujanya C, Ashamol S, Padalkar S and Radhakrishnan S. Control of nanoparticle size of fillers by polymer blend technique Polymer 2001; 42(5): 2255–2258.

16.

Das

Pathak

Pramanik

. Low-temperature preparation of nanocrystalline lead zirconate titanate and lead lanthanum zirconate titanate powders using triethanolamine. J Am Ceramic Soc 81(12): 3357–3360.

17.

Pathak

Panda

Tarafdar

Pramanik

. Synthesis of nano-sized metal oxide powders and their application in separation technology. J Indian Chem Soc 2003; 80: 289–295.

18.

Abdul

Patil

Mahulikar

Kapadi

Hundiwale

. Studies on processing of styrene butadiene rubber (SBR).CaCO₃ nanocomposites by different mixing techniques and their performance properties. Rubber India Lxi 2009; (06): 29–36.

19.

Starnes

. Structural and mechanistic aspects of the thermal degradation of poly(vinyl chloride). Prog Polym Sci 2002; 27: 2133–2170.

20.

Benes

Milanov

Matuschek

Placek

Balek

. Thermal degradation f PVC cable insulation studied by simultaneous TG-FTIR and TG-EGA methods. J Therm Anal Calorim 2004; 78(2): 621–630.

21.

Karayildirim

Yanik

Yuksel

Saglam

Vasile

Bockhorn

. The effect of some fillers on PVC degradation. J Anal Appl Pyrol 2006; 75(2): 112–119.

22.

Peng

Mingfei

Jinshan

. Thermal stabilities of poly(vinylchloride)/ calcium carbonate (PVC/CaCO₃) composites. J Macromol Sci B Phys 2006; 45: 1135–1140.

23.

Chen

Teng

Yang

. Effects of microscale calcium carbonate and nanoscale calcium carbonate on the fusion, thermal, and mechanical characterizations of rigid poly(vinyl chloride)/calcium carbonate composites. J Polym Sci B Polym Phys 2006; 44: 451–460.

Evaluation of the synergistic effect of layered double hydroxides with micro- and nano-CaCO 3 on the thermal stability of polyvinyl chloride composites

Abstract

Keywords

Introduction

Experiment

Materials

Synthesis of zinc glutarate

Synthesis of nano-sized CaCO3

Preparation of the PVC/CaCO3 nanocomposites

Characterization

X-Ray diffraction and transmission electron microscopy (TEM)

Thermogravimetric analysis

Scanning electron microscopy

Mechanical testing

Results and discussion

Particle size determination

Particle size of synthesized CaCO3 nanoparticles confirmed from TEM

Thermal stability of PVC

Morphological study

Mechanical testing

Conclusion

Footnotes

Acknowledgement

Funding

References

Synthesis of nano-sized CaCO₃

Preparation of the PVC/CaCO₃ nanocomposites

Particle size of synthesized CaCO₃ nanoparticles confirmed from TEM