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Method for determining the photocatalytic potential of portland cement mortar containing TiO2 for decomposing the pollutant nitrogen monoxide

Abstract

Photocatalytic materials can minimize atmospheric pollution by decomposing certain organic and inorganic pollutants using sunlight as an energy source. In this paper, the development of a methodology to measure the photocatalytic potential of mortar containing TiO2 nanoparticles is reported. The results indicate that up to 40% of NOx can be degraded by Portland cement mortar containing 30-50% of TiO2, which validates the method developed for evaluating the photocatalytic potential of materials.

photocatalytic potential; titanium dioxide; Portland cement mortar; atmospheric pollutants


NOTA TÉCNICA

Method for determining the photocatalytic potential of portland cement mortar containing TiO2 for decomposing the pollutant nitrogen monoxide

Marcelle M. BonatoI; Mariana O. G. P. BragançaII; Kleber F. PortellaII,* * e-mail: portella@lactec.org.br ; Mateus E. VieiraI; Eliseu EsmanhotoII; Dailton P. CerqueiraIII; Jeannette C. M. dos SantosIII

IUniversidade Federal do Paraná, Centro Politécnico da UFPR, 81531-980 Curitiba - PR, Brasil

IIInstituto de Tecnologia para o Desenvolvimento, Centro Politécnico da UFPR, 81531-980 Curitiba - PR, Brasil

IIICompanhia de Eletricidade do Estado da Bahia, Av. Edgar Santos, nº 300, 41180-790 Salvador - BA, Brasil

ABSTRACT

Photocatalytic materials can minimize atmospheric pollution by decomposing certain organic and inorganic pollutants using sunlight as an energy source. In this paper, the development of a methodology to measure the photocatalytic potential of mortar containing TiO2 nanoparticles is reported. The results indicate that up to 40% of NOx can be degraded by Portland cement mortar containing 30-50% of TiO2, which validates the method developed for evaluating the photocatalytic potential of materials.

Keywords: photocatalytic potential; titanium dioxide; Portland cement mortar; atmospheric pollutants.

INTRODUCTION

Since discovery of photocatalytic splitting of water by suspensions of titanium dioxide (TiO2) initially by Fujishima and Honda in 1972 and subsequently studied by Nogueira and Jardim (1998),1 researchers have been investigating its mechanism and trying to improve its photocatalytic efficiency. TiO2, a semiconductor (Egap = 3.2 eV), forms three crystalline structures: anatase, rutile, and brokita. Anatase has a higher photocatalytic activity and is used largely due to its high efficiency and low cost. Its principle of operation is based on the generation of electron-hole pair upon absorbing UV light energy. Upon irradiation, electrons in the valence band receive enough power to overcome the energy gap of TiO2, and thus can be transferred to the conduction band leaving vacancies called holes in the valence band.1 These electron-hole pairs are strong oxidizing agents and are responsible for the digestion of various organic compounds. Several studies have investigated the possible applications of TiO2 as a photocatalytic material.2

Minimization of the impact of gas pollutants on environment by photocatalysis is a widely pursued goal; several researchers have studied the decomposition of NOx (Poon and Cheung, 2007; Hüsken et al., 2009), NH3 (Jin et al., 2009), and other harmful organic compounds, such as benzene (Du et al., 2011), toluene (Demeestere et al., 2008), and acetone (Visinescu et al, 2005), into innocuous substances.3

The use of this technique in civil engineering began in the 1990s in Japan, where companies and universities began to evaluate the photocatalytic abilities of concrete and ceramic tiles.4

Thus, in order to implement the technology, a methodology is developed to measure the photocatalytic potential of Portland cement mortar containing TiO2 nanoparticles in a controlled environment with an UV-A lamp radiation and a known concentration of NOx gas input.

EXPERIMENTAL

Materials

The cement used in this work was the CP II-32 Z (Portland cement composite with addition of pozzolan), due to its wide use in construction, plain concrete, reinforced concrete, prestressed concrete, precast elements, and other artifacts. Moreover, the material exhibits low permeability, allowing for an ideal application, as recommended by the Brazilian ABNT NBR 11579/91.5

Natural washed sand, as fine aggregate, was used for the production of mortar. The water from Curitiba-PR (Brazil) public water supply, considered potable, was used for mixing the concrete strength.

Commercial TiO2 Evonik Aeroxide P25, predominantly composed of anatase phase, was used as the photocatalytic substance. The primary particle size and surface area of TiO2 powder was 21 nm and 50 ± 15 m2 g-1, respectively, as specified in the datasheet.

Methodology

Material characterization

Cement and fine aggregate material selected for use in the present study were characterized in accordance with the Brazilian standards (ABNT). Physical, chemical, and mechanical properties of the materials were observed to ensure that there was no interference in the quality of the produced concreted. Table 1 lists the test and methods adopted for evaluating each material.

X-ray diffraction patterns of TiO2 samples were measured on a Philips X'Pert MPD diffractometer with Cu-Ka radiation operating at 40 kV and 50 mA. The diffraction patterns were used to identify the structural phase of the sample and the Scherrer equation was used to identify the crystallite size:

where the value of k, the form factor, is 0.90 for a sphere; λ = 1.5406 Å; , base value at half-height (radians); and θ is the diffraction angle.

Scanning electron microscopy (SEM) measurements were carried out on a Philips XL 30 equipped with microprobe analytical X-ray type EDS. The sample TiO2 powder was previously covered with a thin layer of gold.

Photocatalytic mortar dosages

The photocatalytic study was conducted on samples of simple mortar (thickness = 1.8 cm), covered with a layer of photocatalytic mortar (thickness = 0.2 cm). Simple mortar with cement:sand (2.4 mm):water weight ratio of 1:3:0.4 were prepared. For the photocatalytic mortar layer, the ratio of the components was the same, except that various concentrations of TiO2 (as cement substitute) were used, according to the data presented in Table 2.

The samples were dry cured for ~48 h and wet cured for ~1 week before the tests were conducted for determining the photocatalytic potential.

Photocatalytic test

The photocatalytic potential of Portland cement mortar samples containing varying amounts of TiO2 was measured using an in-house built PVC cell (100 mm diameter) equipped with a UV-A lamp irradiating UV light between the wavelengths 320 and 400 nm directly on the sample, as shown in Figure 1. The oxidation and consumption of gas by the photocatalytic TiO2 were determined by analyzing the absorption/reaction of NOx, a gas representative of pollutants. Two additional components were used for this: a) a zero air generator (ZAG 7001) and a computerized calibrator (MGC 101) (both Environnement model) were used to adjust the initial concentration of the NOx gas injected in the cell, and b) the environmental air monitor (Horiba) was used to recognize the input and output concentration of NOx. The concentration of NOx inlet was set at 1.2 ppm, since the same concentration has been used by other researchers performing similar NOx degradation studies, and also because the usual concentration in several Brazilian environments (as stipulated by the Brazilian laws) are below this.6 The flow rate was set at 0.7 L/min, and the test was carried out over a 50 min period. The performance of the samples was assessed over time of exposure to the gas and UV-A radiation.


RESULTS AND DISCUSSION

Specific results obtained from each experiment are presented and discussed below.

Materials characterization

The cement was characterized in accordance with the Brazilian standards and the results are listed in Table 3. The results indicate that the properties of the cement are in accordance to the ABNT standards and the recommendations of the manufacturer.

The characteristics of the natural sand, including its particle size distribution, indicate that it is suitable for use in mortar (Table 4).

XRD patterns of TiO2 (Figure 2) indicate that the predominant phase is the anatase, which is considered to be photochemically active. From the high intensity diffraction peaks at 2θ values of 25º and 52º, the average grain size of crystallites is calculated to be 18 nm.


SEM micrograph of the TiO2 powder is shown in Figure 3 and shows that the powder has a uniform texture with fine grains. EDS analysis indicates that the sample is predominantly composed of titanium and oxygen.


Photocatalytic tests

Figure 4 displays two results from the photocatalytic degradation of NOx gas by the mortar samples with 10% TiO2 (weight/weight). These measurements are conducted in the presence of NOx gas (1.2 ppm) and UV-A radiation. Both samples present a 38 ± 1% reduction in NOx gas during the ~35 min analysis period. The efficiency of the method can be viewed during the period the UV-A lamp is turned on. These results confirm that TiO2 oxidizes the environmental pollutant, NOx gas.


The average results for oxidation of NOx by mortar samples containing different concentrations of TiO2 are shown in Figure 5. From the results, it can be noted that samples with different concentrations of TiO2 mortar when irradiated by UV light are capable of oxidizing NOx gas pollutants. When compared with the reference material (without TiO2), 40% of the NOx is photocatalytically degraded in the presence of mortar containing varying amounts of TiO2.


The mechanism of photocatalytic oxidation of NOx can be represented by Equations (1-9).7

Equation (1) presents the absorption of photons (hν) of UV-A radiation by the semiconductor TiO2, resulting in the transfer of an electron (e-) from the valence to the conduction band with generation of a hole h+ in the valence band. The equations (2-4) show the adsorption of the reagents H2O, O2, and NO by TiO2. The water molecules adsorbed on the surface of the semiconductor generate hydroxyl radicals (OH•), as demonstrated in the equations (5 and 6). Subsequently, these radicals are involved in the oxidation of NO and NO2 to NO3 (Equations (7-9)). Thus, the nitrates ions are the degradation products of NOx.

It is evident from the graph that the higher rate of NOx degradation is observed when there is a 30-50% content of photoactive material. It is not environmentally suitable and financially feasible to use larger volumes of material.

CONCLUSION

A method to evaluate the photocatalytic efficiency of TiO2 for the oxidation of pollutants, such as NOx gas, is developed. When a layer of the mortar containing 30-50% TiO2 is irradiated under a UV light, up to 40% of NO can be reduced.

Besides, incorporation of photocatalytic agents in the mortar for the construction of various concrete artifacts is a very promising technique for minimizing pollutants, which can used on different objects, such as in electric poles for power distribution.

ACKNOWLEDGEMENTS

The present study utilized financial resources, materials, and additional infrastructure of LACTEC, ANEEL, COELBA, P&D 0047-002/2009 and CNPq Lei 8010/90. Thus, the project team is thankful to the CNPq/PQ and CNPq/PIBITI for the scholarships provided.

REFERENCES

1. Nogueira, R. F. P.; Jardim, W.; Quim. Nova 1998,21,69.

2. Silva, S. S.; Magalhães, F.; Sansiviero, M. T. C.; Quim. Nova 2010,33,85; Segato, T.P.; Technical Report. UEL, Londrina, 2004.

3. Yu, J-G.; Yu, H-G.; Cheng, B.; Zhao, X-J; Yu, J. C.; Ho, W-K.; J. Phys. Chem. B 2003,107,13871; Poon, C. S.; Cheung, E.; Constr. Build. Mater. 2007,21,1746; Hüsken, G.; Hunger, M.; Browers, H. J. H; Build. Environ. 2009,44,2463; Demeestere, K.; Dewulf, J.; De Witte, B.; Beeldens, A.; Van Langenhove, H.; Build. Environ. 2008,43,406; Kuo, C. C.; Tseng, Y-H.; Lin, H-Y.; Huang, C-H.; Shen, C-Y.; Li, Y. Y.; Shah, S.I.; Huang, C-P.; J. Am. Chem. Soc. 2007,129,4538; Maggos, T.; Plassais, A.; Bartzis, J. G.; Vasilakos, C.; Moussiopoulos, N.; Bonafous, L.; Environ. Monit. Assess. 2008,136,35; Linsebigler, A. L.; Lu, G.; Yates, J. T.; Chem. Rev. 1995,95,735; Jin, R.; Wu, Z.; Liu, Y.; Jiang, B.; Wang, H.; J. Hazard. Mater. 2009,161,42; Visinescu, C. M.; Sanjines, R.; Lévy, F.; Pârvulescu, V. I.; Appl. Catal., B 2005,60,155; Du, J.; Chen, W.; Zhang, C.; Liu, Y.; Zhao, C.; Dai, Y.; Chem. Eng. J. 2011,170,53.

4. Luca, D.; Teodorescu, C. M.; Apetrei, R.; Macovei, D.; Mardare, D.; Thin Solid Films 2007,515,8605.

5. ABNT_NBR 11579; Cimento Portland - Determinação da finura por meio da peneira 75 µm (nº 200). Rio de Janeiro, 1991; NBR NM 76; Cimento Portland - Determinação da finura pelo método de permeabilidade ao ar (Método de Blaine). Rio de Janeiro, 1998; NBR 11582; Cimento Portland - Determinação da expansibilidade de Le Chatelier. Rio de Janeiro, 1991; NBR NM 43; Cimento Portland - Determinação de Pasta de Consistência Normal. Rio de Janeiro, 2003; NBR NM 23; Cimento Portland - Determinação de massa específica. Rio de Janeiro, 2001; NBR NM 65; Cimento Portland - Determinação do tempo de pega. Rio de Janeiro, 2003; NBR 7215; Cimento Portland - Determinação da resistência à compressão. Rio de Janeiro, 1997; NBR 11578; Cimento Portland composto - Especificação. Rio de Janeiro, 1991; NBR NM 18; Cimento Portland - Determinação de Perda ao Fogo. Rio de Janeiro, 2004; NBR NM 15; Cimento Portland - Análise Química - Determinação de Resíduo Insolúvel. Rio de Janeiro, 2004; NBR NM 21; Cimento Portland - Análise química - Método optativo para a determinação de dióxido de silício, óxido de alumínio, óxido férrico, óxido de cálcio e óxido de magnésio. Rio de Janeiro, 2004; NBR NM 11-2; Cimento Portland - Análise química - Determinação de óxidos principais por complexometria Parte 2: Método ABNT. Rio de Janeiro, 2009; NBR 7211; Agregados para concreto - Especificação. Rio de Janeiro, 2005; NBR 7217; Determinação da composição granulométrica dos agregados. Rio de Janeiro, 1982; NBR 6118; Projeto de estruturas de concreto - Procedimento. Rio de Janeiro, 2007; NBR NM 53; Agregado graúdo - Determinação da massa específica, massa específica aparente e absorção de água. Rio de Janeiro, 2009; NBR NM 45; Agregados - Determinação da massa unitária e do volume de vazios. Rio de Janeiro, 2006; NBR NM 30; Agregados miúdos - Determinação da absorção de água. Rio de Janeiro, 2001; NBR 7218; Agregados - Determinação do teor de argila em torrões e materiais friáveis. Rio de Janeiro, 2010.

6. Maggos, T.; Bartzis, J. G.; Leva, P.; Kotzias, D.; Appl. Phys. A: Mater. Sci. Process. 2007,89,81; Ballari, M. M.; Hunger, M.; Sken, G. H.; Brouwers, H. J. H.; Catal. Today 2010,151,71.

7. Melo, J. V. S.; Trichês, G.; Build. Environ. 2012,49,117.

Recebido em 19/09/2013; aceito em 26/02/2014; publicado na web em 17/06/2014

  • 1. Nogueira, R. F. P.; Jardim, W.; Quim. Nova 1998,21,69.
  • 2. Silva, S. S.; Magalhães, F.; Sansiviero, M. T. C.; Quim. Nova 2010,33,85;
  • Segato, T.P.; Technical Report. UEL, Londrina, 2004
  • 3. Yu, J-G.; Yu, H-G.; Cheng, B.; Zhao, X-J; Yu, J. C.; Ho, W-K.; J. Phys. Chem. B 2003,107,13871;
  • Poon, C. S.; Cheung, E.; Constr. Build. Mater. 2007,21,1746;
  • Hüsken, G.; Hunger, M.; Browers, H. J. H; Build. Environ. 2009,44,2463;
  • Demeestere, K.; Dewulf, J.; De Witte, B.; Beeldens, A.; Van Langenhove, H.; Build. Environ. 2008,43,406;
  • Kuo, C. C.; Tseng, Y-H.; Lin, H-Y.; Huang, C-H.; Shen, C-Y.; Li, Y. Y.; Shah, S.I.; Huang, C-P.; J. Am. Chem. Soc. 2007,129,4538;
  • Maggos, T.; Plassais, A.; Bartzis, J. G.; Vasilakos, C.; Moussiopoulos, N.; Bonafous, L.; Environ. Monit. Assess. 2008,136,35;
  • Linsebigler, A. L.; Lu, G.; Yates, J. T.; Chem. Rev. 1995,95,735;
  • Jin, R.; Wu, Z.; Liu, Y.; Jiang, B.; Wang, H.; J. Hazard. Mater. 2009,161,42;
  • Visinescu, C. M.; Sanjines, R.; Lévy, F.; Pârvulescu, V. I.; Appl. Catal., B 2005,60,155;
  • Du, J.; Chen, W.; Zhang, C.; Liu, Y.; Zhao, C.; Dai, Y.; Chem. Eng. J. 2011,170,53.
  • 4. Luca, D.; Teodorescu, C. M.; Apetrei, R.; Macovei, D.; Mardare, D.; Thin Solid Films 2007,515,8605.
  • 5. ABNT_NBR 11579; Cimento Portland - Determinação da finura por meio da peneira 75 µm (nº 200). Rio de Janeiro, 1991;
  • NBR NM 76; Cimento Portland - Determinação da finura pelo método de permeabilidade ao ar (Método de Blaine). Rio de Janeiro, 1998;
  • NBR 11582; Cimento Portland - Determinação da expansibilidade de Le Chatelier. Rio de Janeiro, 1991;
  • NBR NM 43; Cimento Portland - Determinação de Pasta de Consistência Normal. Rio de Janeiro, 2003;
  • NBR NM 23; Cimento Portland - Determinação de massa específica. Rio de Janeiro, 2001;
  • NBR NM 65; Cimento Portland - Determinação do tempo de pega. Rio de Janeiro, 2003;
  • NBR 7215; Cimento Portland - Determinação da resistência à compressão. Rio de Janeiro, 1997;
  • NBR 11578; Cimento Portland composto - Especificação. Rio de Janeiro, 1991;
  • NBR NM 18; Cimento Portland - Determinação de Perda ao Fogo. Rio de Janeiro, 2004;
  • NBR NM 15; Cimento Portland - Análise Química - Determinação de Resíduo Insolúvel. Rio de Janeiro, 2004;
  • NBR NM 21; Cimento Portland - Análise química - Método optativo para a determinação de dióxido de silício, óxido de alumínio, óxido férrico, óxido de cálcio e óxido de magnésio. Rio de Janeiro, 2004;
  • NBR NM 11-2; Cimento Portland - Análise química - Determinação de óxidos principais por complexometria Parte 2: Método ABNT. Rio de Janeiro, 2009;
  • NBR 7211; Agregados para concreto - Especificação. Rio de Janeiro, 2005;
  • NBR 7217; Determinação da composição granulométrica dos agregados. Rio de Janeiro, 1982;
  • NBR 6118; Projeto de estruturas de concreto - Procedimento. Rio de Janeiro, 2007;
  • NBR NM 53; Agregado graúdo - Determinação da massa específica, massa específica aparente e absorção de água. Rio de Janeiro, 2009;
  • NBR NM 45; Agregados - Determinação da massa unitária e do volume de vazios. Rio de Janeiro, 2006;
  • NBR NM 30; Agregados miúdos - Determinação da absorção de água. Rio de Janeiro, 2001;
  • NBR 7218; Agregados - Determinação do teor de argila em torrões e materiais friáveis. Rio de Janeiro, 2010
  • 6. Maggos, T.; Bartzis, J. G.; Leva, P.; Kotzias, D.; Appl. Phys. A: Mater. Sci. Process. 2007,89,81;
  • Ballari, M. M.; Hunger, M.; Sken, G. H.; Brouwers, H. J. H.; Catal. Today 2010,151,71.
  • 7. Melo, J. V. S.; Trichês, G.; Build. Environ. 2012,49,117.
  • *
    e-mail:
  • Publication Dates

    • Publication in this collection
      01 Aug 2014
    • Date of issue
      July 2014

    History

    • Accepted
      26 Feb 2014
    • Received
      19 Sept 2013
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