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Application of bauxite waste from amazon region in the heavy clay industry

Abstract

In this work, a method was developed for the application of red mud, an alkaline leaching waste, from a bauxite processing plant located in northern Brazil (Amazon region) as starting material for heavy clay products. Samples were prepared by pressing blends of red mud and clay, which were then fired at temperatures from 900 ºC to 1190 ºC. Characterization was carried out by chemical analysis, differential thermal analysis (DTA) and X-ray diffraction (XRD), and the following ceramic properties were evaluated: water absorption, linear shrinkage and flexural strength. In order to evaluate the Na+ stability in the dense ceramic, leaching tests were also carried out on the specimens after sintering process. Results indicated that samples with 50 and 70 wt% of red mud are proper for being used in the production of ceramic bodies, due to its excellent properties, mainly high mechanical resistance and low water absorption, showing thus, an option to minimizing the environmental impacts caused by the aluminum industry.

traditional ceramics; red mud; bauxite waste


Application of bauxite waste from amazon region in the heavy clay industry

Edemarino Araujo HildebrandoI,* * e-mail: edemarino@ufpa.br ; José Antônio da Silva SouzaII; Rômulo Simões AngélicaIII; Roberto de Freitas NevesII

IFaculty of Materials Engineering, Federal University of Pará – UFPA, Folha 17, Quadra 04, Lote Especial, CEP 68505-080, Marabá, PA, Brazil

IIFaculty of Chemical Engineering, Federal University of Pará – UFPA, Av. Augusto Corrêa s/n, CEP 66075-110, Belém, PA, Brazil

IIIFaculty of Geology, Federal University of Pará – UFPA, Av. Augusto Corrêa s/n, CEP 66075-110, Belém, PA, Brazil

ABSTRACT

In this work, a method was developed for the application of red mud, an alkaline leaching waste, from a bauxite processing plant located in northern Brazil (Amazon region) as starting material for heavy clay products. Samples were prepared by pressing blends of red mud and clay, which were then fired at temperatures from 900 ºC to 1190 ºC. Characterization was carried out by chemical analysis, differential thermal analysis (DTA) and X-ray diffraction (XRD), and the following ceramic properties were evaluated: water absorption, linear shrinkage and flexural strength. In order to evaluate the Na+ stability in the dense ceramic, leaching tests were also carried out on the specimens after sintering process. Results indicated that samples with 50 and 70 wt% of red mud are proper for being used in the production of ceramic bodies, due to its excellent properties, mainly high mechanical resistance and low water absorption, showing thus, an option to minimizing the environmental impacts caused by the aluminum industry.

Keywords: traditional ceramics, red mud, bauxite waste

1. Introduction

Mining wastes accumulate at higher rates as a consequence of the increasing consumption of metals in the world and the growing exploitation of mineral deposits. Their disposal raises several environmental situations. Special problems occur related to residues which contain heavy metal ions, surfactants, acids, etc., which may affect surface and underground water quality1,2. One of these wastes, known as red mud, contains a significant amount of oxides, such as ferric oxide, calcium oxide, titanium and sodium oxide, among others, that are the main constituents, besides trace elements like Ga, V, Sr, Zr, Y, Th, U, etc. Most of these compounds are originally present in the bauxites and others are added during Bayer process for the alumina production (e.g., NaO)[3]. The presence of such alkaline oxides in the red mud lead to a corrosive action on metals, siliceous materials and living beings4.

Solving or minimize these problems involves mainly an improvement and a better optimization of production in order to generate the least amount of waste. Among the several industrial segments, the alumina industry faces a world-class problem namely the increasing disposal of solid wastes that is very common in the Bayer processing5,6. Generally, 0.8-1.5 tons of red mud is generated from each ton of alumina produced. With the quick development of alumina industry all over the world, the disposal of red mud has caused serious environmental problems mainly due to its large quantities and strong alkalinity (pH 10.0-12.5)[7]. As same bauxites contain radioactive elements, the red mud, has characteristic radioactivity, which can accumulate in the dam construction and storage yards endanger human health4.

Tsakiridis et al.8 estimated that over 66 million tons of red mud is impounded annually in the world (around 85 alumina plants worldwide). The disposal of such a huge amount of alkaline waste is very expensive (up to 1-2% of the alumina price), and requires large areas of occupation (approximately 1 km2 per 5 years for a 1 Mtpy alumina plant). Alunorte company, located at Pará State in the Brazilian Amazonia, produces 4.40 million tons/year of alumina, with an expected 6.26 million tons/year capacity9 which will produce an even larger volume of red mud as waste.

As a corrosively hazardous material, the comprehensive utilization of red mud has attracted more and more interest from the scientific community. Thus, a number of efforts have been made in order to find possible applications for this material, as for example, as catalysts materials10, fillers in PVC11, pigment12, for the recovery of some valuable elements13, cements manufacturing8,14-16, water treatment17,18, among others. Unfortunately, several reuse techniques consume relatively small amounts of waste compared to the huge amount produced. Therefore, one of the most appealing application should be the reuse of red mud as a starting material for the production of construction and building materials4,19-22. Sglavo et al.20 investigated the use of red mud as a raw component in clay mixtures for ceramic bodies production and the influence in the amount of red mud (0-20 wt%) and sintering temperature (950-1050 ºC) on the final properties of the produced material was analyzed. Recently, Qin and Wu4, prepared a novel ceramic material at 1020-1050 ºC using 30 wt% of red mud. The authors investigated the radiation level, and concluded that the ceramic materials produced using red mud are not harmful to humans beings or to the environment.

Considering all the concerns described above, the main purpose of the present work was to develop a method to verify how the bauxite waste (red mud) from Brazilian Amazon region could be used as a raw material in the ceramic industry, using it not only as an additive, i.e., in small quantities, but in high concentrations. Thus, studies were performed about the ceramic properties of the sintered material and the data were compared with the values found in scientific literature directed to red ceramics. Leaching tests on the final products were also carried.

2. Material and Methods

2.1. Raw materials

The red mud studied in this work was supplied by Alunorte company (Amazon region, Para State, Brazil. The sample was collected directly from the tailings basin and its moisture content is around 9%. The clay used for the blends occurs as a compact brown material with red mottling related to tertiary geological formations. Samples were collected from outcrops located nearby the Alunorte plant.

The raw materials were characterized by X-ray diffraction (XRD), differential thermal analysis (DTA) and chemical analysis. The mineralogical composition of the bulk materials (randomly oriented samples) was carried out by Powder X-ray diffractometry (XRD), using a Panalytical X'Pert PRO MPD (PW3040/60) diffractometer with a ceramic X-ray tube (λ CuKα1=0.1540598 nm), Kβ Ni filter and a X´celerator PSD (Position-Sensitive Detector). The following analysis conditions were used: scan range from 5 to 70º 2θ, 40 kV and 30 mA, 0.02º step size and 10s time/step; divergent slit of 1/4º and anti scattering of 1/2º; mask of 10 mm; sample movement set to spinning with a rotation time of 1.0 s. Differential thermal analysis (DTA) of ≈ 17 mg of sample were carried out in a Thermal Science Thermoanalyzer model PL-STA. The experiments used alumina crucibles and N2 atmosphere with a flow rate of 50 cc min–1 at a heating time of 20 ºC min−1 to 1100 ºC. Total chemical analysis (major oxides and trace elements) were obtained by using a combination of methods, including wet analytical methods and Atomic Absorption Spectrometry.

2.2. Sample preparation and sintering methods

Samples of clay and red mud were dried at 110 ºC until constant weight, mixed and homogenized with water, using the following proportions: 70 wt% red mud / 30 wt% clay and 50 wt% red mud/50 wt% clay; the percentages of red mud were established from Hildebrando et al.23. The mixtures were then dried at 110º C/24 h, grinded and screened through a 80 Mesh Tyler sieve. Batches of eight green specimens (10.0 cm × 5.0 cm × 1.0 cm bodies) were pressed (axial compressive strength) at 20 MPa.

The ceramic bodies were named as follow: RM-50 (50% red mud and 50% clay) and RM-70 (70% red mud and 30% clay). During firing in a muffle electrical furnace, the heating and cooling rates were kept at 10 ºC/min and the specimens were maintained at the maximum temperature (900 ºC, 950 ºC, 1000 ºC, and 1190 ºC) for 3 hours. Such sintering temperatures were used according to Monteiro and Vieira24, and several others references from the scientific and technological literature.

2.3. Mechanical properties

The samples were submitted to the following tests: water absorption (WA) determined from the weight differences between the as-sintered and water soaked samples (immersed in boiling water for 2 hours), linear shrinkage (LS) evaluated from the variation of the length of the rectangular pieces, and flexural strength (FS). Flexural strength was obtained by the three points bend test performed in a universal test machine25,26.

2.4. Sodium contents in the samples after sintering

Samples were submitted to leaching tests, according to the technical standard NBR 10005[27], in order to detect possible polluting factors from the soluble sodium in the ceramic bodies.

3. Results and Discussion

The chemical composition of the raw materials dried at 110 ºC is shown in Table 1.

Red mud possesses high amount of fusing material, as expected, such as sodium and iron which can reduce the sintering temperature for adequately formulated mixtures. The amount of silica (SiO2) present in the red mud is low (19.9%) so it cannot be used alone as it is not enough to form the glass that would give mechanical resistance to the sintered material.

The clay is mainly constituted by SiO2 (51.8%), Al2O3 (24.5%) and Fe2O3 (10.9%) and a low amount of fusing compounds (Na2O + K2O < 0.35%). These features render the clay economically unfit for use in red ceramic products, due to its high sintering temperatures.

The differential thermal analysis (DTA) for the clay, shown in Figure 1, portrays two endothermic peaks, one at 130 ºC due to water loss and another at 550 ºC due to dehydroxilation that is characteristic to kaolinite. Right after these peaks a low intensity exothermic peak is observed near the 970 ºC, characteristic of the formation of the silicon-aluminum spinel28.


The DTA for the red mud, shown in Figure 1, portrays a wide endothermic band in the range 100 ºC-280 ºC and can be discussed in two parts. The first in the range 100 ºC-150 ºC is related with the evaporation of physical water content of the red mud while the second part 150 ºC-280 ºC can be explained by the loss of zeolitic water and by the dehydrolixation of ferrous compounds; these bands are in good agreement with the reported by Castaldi et al.29. The endothermic peak at 310 ºC corresponds to the temperature of decomposition of gibbsite29, and that acoording to Atasoy30 gibbsite partially dehydroxylates to boehmite and the remained part of the gibbsite goes to a transition of alumina at 314 ºC.

Figure 2 presents the X-ray patterns of red mud and clay dried at 110 ºC. In general, the minerals that are present in the sample of red mud, can be identify and classify in two categories. In the first, phases from bauxite such as gibbsite, hematite, goethite, anatase and quartz; this results are similar to those reported by Rivas Mercury et al.31. The second category, phases formed during Bayer process such as sodalite and cancrinite29. In turn, the clay is constituted mostly by the clay mineral kaolinite and other mineral phases such as hematite, quartz and anatase.


Figure 3 and 4 displays the results of ceramic properties conducted on the bodies after sintering process. Figure 3 shows the curves for water absorption and linear shrinkage. This type of curves is also known as gresification diagram, which is associated with the efficiency of the sintering process. The sintering of a material usually causes many changes in its properties. In ceramics, the changes generally are accompanied by shrinkage as the temperature is increased. During this process, the particles are bound together, reducing porosity and making difficult the water absorption by the material23. In general, the curves in Figure 3 show a decrease in the water absorption values as the linear shrinkage is increased, while the sintering is carried out. According to Brazilian norms32,33 the maximum water absorption for bricks and roofing tiles are 22% and 20%, respectively. It is observed in Figure 3 that the specification for bricks roofing tiles was achieved in the studied temperature range (900-1150 ºC) for sample RM-50 while the sample RM-70 attained only above 950 ºC



One of the most significant modifications of the ceramic products after sintering is the improvement in its mechanical resistance34. Samples RM-70 and RM-50 showed an increasing trend in such values, and this is substantiated by the presence of alkaline fluxes in the formulations from red mud, which cause densification by liquid phase sintering with the creating more glass phases to form glass network structures. It is important mentioning that the values measured (>10 MPa) were above the limits recommended for red ceramics by technical standards32,33 and were better that found in previous works20. Figure 4 evidenced the variation with temperature of the flexural strength for the samples studied.

As can be seen in Figure 5, the concentration of sodium decreased at higher sintering temperatures. This is due to reactions mainly between sodium present in the red mud and silicates in the clay, when both raw materials are blended. This strongly contributes for the formation of more vitreous phase in the sintered material.


For both samples (RM-70 and RM-50) the concentrations of sodium were into a tolerable range, given the limit of 200 ppm adopted by the Ministry of Health – Brazilian Standard for Fresh Water. This reveals that products fabricated from the mixtures of red mud and clay in both compositions would not be aggressive to the environment and would classify as Waste Class III – inert according to standards NBR 1000435.

4. Conclusions

The application of red mud in mixtures with clay offers an interesting alternative for the fabrication of products of heavy clay industry, especially because of the low cost of raw materials, in particular the red mud which is produced in large quantities as bauxite processing waste. Samples with 50 and 70 wt% of red mud demonstrated all the possibilities of being used in the production of bricks and compact blocks given their excellent qualities mainly high mechanical resistance and low water absorption. The sintering process that took place into the mixture of clay and red mud was able to fix the soluble sodium which was largely present in the mixture. The leaching tests showed that the increasing in sintering temperature led to a decreasing in concentration of sodium residuals, owing to reactions that occurred during sintering. Further studies should be performed in order to check the occurrence of efflorescence of soluble salts and leaching from other metals present in the red mud should be evaluated.

Acknowledgements

The authors would like to thank the Brazilian agency CAPES for financial support.

Received: September 26, 2012;

Revised: July 19, 2013

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  • Publication Dates

    • Publication in this collection
      03 Sept 2013
    • Date of issue
      Dec 2013

    History

    • Received
      26 Sept 2012
    • Accepted
      19 July 2013
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