Evaluation of the Antibacterial Activity of a Geopolymer Mortar Based on Metakaolin Supplemented with TiO 2 and CuO Particles Using Glass Waste as Fine Aggregate

: Metakaolin-based geopolymer cements were produced by alkaline activation with a potassium hydroxide and potassium silicate solution. To produce the geopolymer composites, 10 wt.% titanium oxide (TiO 2 ) and 5 wt.% copper oxide (CuO) nanoparticles were used. The geopolymer mortar was prepared using glass waste as ﬁne aggregate. The raw materials and materials produced were characterized by X-ray di ﬀ raction, electron microscopy, and Fourier-transform infrared spectroscopy techniques. Likewise, the geopolymer samples were characterized to determine their physical properties, including their density, porosity, and absorption. The photocatalytic activity of the materials was evaluated by activating the nanoparticles in a chamber with UV–Vis light during 24 h; then, di ﬀ erent tests were performed to determine the growth inhibition of Staphylococcus aureus , Escherichia coli , and Pseudomonas aeruginosa bacteria in nutrient agar for times of up to 24 h. The study results showed that a geopolymer mortar containing glass waste as ﬁne aggregate (GP-G) exhibited a water absorption 56.73% lower than that of the reference geopolymer paste without glass (GP). Likewise, glass particles allowed the material to have a smoother and more homogeneous surface. The pore volume and density of the GP-G were 37.97% lower and 40.36% higher, respectively, than those of the GP. The study with bacteria showed that, after 24 h in the culture media, the GP-G mortars exhibited a high inhibition capacity for the growth of P. aeruginosa from solutions of 10 − 4 mL and in solutions of 10 − 6 mL for E. coli and S. aureus. These results indicate the possibility of generating antibacterial surfaces by applying geopolymer composite. MK and nanoparticles of TiO 2 (10 wt.%) and CuO (5 wt.%) were produced. This study evaluated the physical and microstructural properties of the geopolymers and the functionality of these geopolymers for inhibiting the growth of the bacteria S. aureus, P. aeruginosa , and E. coli. Based on the results obtained, the following conclusions can be drawn:


Introduction
The problematic relationships between environmental pollution and health preservation and prolongation are a subject of current interest and are, therefore, widely studied. Most health problems are associated with the presence of microorganisms such as bacteria, fungi, protozoa, and viruses that commonly infect humans in the living environment, leading to chronic infections and even leading to mortality [1][2][3]. The inanimate surfaces of different materials are often described as the source of hospital outbreaks because their contact with different microorganisms allows microbial permanence for a period of time favoring bacterial proliferation, and they are, therefore, reservoirs of bacteria that cause diseases transmitted through surfaces or fomites. This continues to be a cause of great concern The objective of this preliminary study was to determine the effects of incorporating nanoparticles of metallic oxides, such as TiO 2 and CuO, on the antimicrobial potential of a geopolymeric binder based on metakaolin (MK), and its corresponding geopolymer mortar using glass waste as a fine aggregate. Geopolymer mortars were fabricated for their use as coatings of construction elements for environments susceptible to bacterial growth. Among the microorganisms potentially pathogenic to humans were selected Gram-negative bacteria such as E. coli and Pseudomonas aeruginosa and Gram-positive bacteria such as S. aureus. Infections with these bacteria are recurrent and transmissible to people close to each other [4,5,36,37]. In addition, this preliminary study proposes the direct incorporation of such nanoparticles by mechanically mixing the components of the material in order to directly apply the geopolymer mortar on the substrate surfaces instead of using conventional deposition processes to produce oxide coatings.

Materials
To obtain the geopolymer cement paste, the precursor used was metakaolin (MK MetaMax, BASF, Florham Park, NJ, USA). A mixture of a commercial potassium silicate (SiO 2 = 26.38%, K 2 O = 13.06%, H 2 O = 60.56%), analytical grade potassium hydroxide (KOH), and water was used as an alkaline activator. The cementitious material was formulated using the following molar ratios of oxides, as determined by previous studies: SiO 2 /Al 2 O 3 = 2.5 and K 2 O/SiO 2 = 0.28 [38,39]. To produce the geopolymer composite with photocatalytic and antibacterial properties, titanium oxide (TiO 2 ) and copper oxide (CuO) particles were added. The TiO 2 used was high-purity and analytical grade (Merck, reference 1008081000). The CuO nanoparticles were synthesized from copper acetate ((CH 3 COO) 2 Cu·H 2 O) using the modified Pechini method [40] (Figure 1). To evaluate the cementitious properties, the pastes and mortars were prepared. The mortar was prepared using glass waste (G) as a fine aggregate.
To synthesize the CuO nanoparticles, citric acid and ethylene glycol were initially mixed in 100 mL of distilled water, and the mixture was heated to 70 • C. Then, copper acetate was added. These precursors were mixed with a molar ratio of 1:1:2, and the solution was constantly stirred using a magnetic stirrer. Simultaneously, an NH 4 OH solution was added until a neutral pH (pH = 7) was obtained. The resulting polymeric resin was subjected to an initial thermal treatment at 350 • C; the thermally treated powder was pulverized using a ceramic mortar. The resulting fine powder was thermally treated at 450 • C. The heating rate used in the two heat treatments was adjusted to 10 • C/min.

Preparation of the Geopolymers
To prepare the geopolymers, the components were firstly mixed in a solid state; then, the activating solution was added. The components were mixed for 15 min using a Hobart mixer. Next, the mixture was poured into silicone molds, and discs with 2.5 cm diameters were prepared. The liquid/solid ratio was 0.35 for the pastes and 0.40 for the mortar. The samples were wrapped with a plastic film to prevent moisture from evaporating and kept for 24 h in a chamber with a relative humidity (RH) >90% and a temperature of 25 • C. Subsequently, the samples were demolded and stored for 28 days. Figure 2 shows the experimental methodology followed in the study in order to prepare the geopolymer composites. Table 1 shows the compositions and codes of the mixtures evaluated. Two geopolymer pastes (GP, mGP) were prepared using 10 wt.% titanium oxide (TiO 2 ) and 5 wt.% copper oxide (CuO) particles. The percentage of TiO 2 incorporated was selected based on previous studies [11], where a high photocatalytic capacity for degrading B-rhodamine was achieved using 10 wt.% TiO 2 . Geopolymer mortars (GP-G) were manufactured with a binder/fine aggregate ratio of 1:2 by weight using glass waste (G) as fine aggregate. The photocatalytic capacity of MK-based geopolymer mortars (GP-G) increased up to 72% compared to that obtained with mortars using natural Coatings 2020, 10, 157 4 of 16 sand [41]. Geopolymer mortars with CuO particles were not prepared because the results obtained with the proportion of the oxide used in mGP were negative, as discussed later.
13.06%, H2O = 60.56%), analytical grade potassium hydroxide (KOH), and water was used as an alkaline activator. The cementitious material was formulated using the following molar ratios of oxides, as determined by previous studies: SiO2/Al2O3 = 2.5 and K2O/SiO2 = 0.28 [38,39]. To produce the geopolymer composite with photocatalytic and antibacterial properties, titanium oxide (TiO2) and copper oxide (CuO) particles were added. The TiO2 used was high-purity and analytical grade (Merck, reference 1008081000). The CuO nanoparticles were synthesized from copper acetate ((CH3COO)2Cu•H2O) using the modified Pechini method [40] (Figure 1). To evaluate the cementitious properties, the pastes and mortars were prepared. The mortar was prepared using glass waste (G) as a fine aggregate.   To synthesize the CuO nanoparticles, citric acid and ethylene glycol were initially mixed in 100 mL of distilled water, and the mixture was heated to 70 °C. Then, copper acetate was added. These precursors were mixed with a molar ratio of 1:1:2, and the solution was constantly stirred using a magnetic stirrer. Simultaneously, an NH4OH solution was added until a neutral pH (pH = 7) was obtained. The resulting polymeric resin was subjected to an initial thermal treatment at 350 °C; the thermally treated powder was pulverized using a ceramic mortar. The resulting fine powder was thermally treated at 450 °C. The heating rate used in the two heat treatments was adjusted to 10 °C/min.

Preparation of the Geopolymers
To prepare the geopolymers, the components were firstly mixed in a solid state; then, the activating solution was added. The components were mixed for 15 min using a Hobart mixer. Next, the mixture was poured into silicone molds, and discs with 2.5 cm diameters were prepared. The liquid/solid ratio was 0.35 for the pastes and 0.40 for the mortar. The samples were wrapped with a plastic film to prevent moisture from evaporating and kept for 24 h in a chamber with a relative humidity (RH) >90% and a temperature of 25 °C. Subsequently, the samples were demolded and stored for 28 days. Figure 2 shows the experimental methodology followed in the study in order to prepare the geopolymer composites. Table 1 shows the compositions and codes of the mixtures evaluated. Two geopolymer pastes (GP, mGP) were prepared using 10 wt.% titanium oxide (TiO2) and 5 wt.% copper oxide (CuO) particles. The percentage of TiO2 incorporated was selected based on previous studies [11], where a high photocatalytic capacity for degrading B-rhodamine was achieved using 10 wt.% TiO2. Geopolymer mortars (GP-G) were manufactured with a binder/fine aggregate ratio of 1:2 by weight using glass waste (G) as fine aggregate. The photocatalytic capacity of MKbased geopolymer mortars (GP-G) increased up to 72% compared to that obtained with mortars using natural sand [41]. Geopolymer mortars with CuO particles were not prepared because the results obtained with the proportion of the oxide used in mGP were negative, as discussed later.

Physicochemical and Microstructural Characterization Techniques
The following instrumental techniques were used to characterize the materials:


The chemical composition of the starting materials was determined by X-ray fluorescence (XRF) using a Magix Pro PW-2440 X-ray fluorescence spectrometer (PANalytical, Tollerton,

Physicochemical and Microstructural Characterization Techniques
The following instrumental techniques were used to characterize the materials: • The chemical composition of the starting materials was determined by X-ray fluorescence (XRF) using a Magix Pro PW-2440 X-ray fluorescence spectrometer (PANalytical, Tollerton, Nottingham, UK) equipped with a rhodium tube with a maximum output of 4.0 kW and 0.02% sensitivity.

•
The X-ray diffraction (XRD) patterns were obtained with a RINT2000 wide-angle goniometer using Cu Kα radiation at 45 kV and 40 mA, and data were collected with a step size of 0.02 • over the range of 5 • -60 • 2θ using a scan speed of 5 • /min. • Fourier-transform infrared spectroscopy (FTIR) was performed with a PerkinElmer Spectrum 100 spectrometer operated in transmittance mode, and data were collected for a wavelength range of 450 cm −1 to 4000 cm −1 . The samples were prepared using the compressed KBr method.

•
The morphological observations and particle sizes of TiO2 and CuO were evaluated by scanning electron microscopy (SEM) using a JEOL JSM-6490 LV SEM system operated with an accelerating voltage of 20 kV. The specimens were coated with gold, and the observations were made in vacuum mode.

•
The density, pore volume, and water absorption of the geopolymers were determined following the procedures detailed in the ASTM C642-13 standard, except that the temperature used to dry the sample in the oven was 60 • C for 48 h.

Evaluation of the Antibacterial Activity of the Geopolymeric Materials
The geopolymer samples were exposed to the bacteria under study by activating the materials with UV-A light for 48 h. The UV-A radiation was provided by two mercury lamps (Electrolux T8 20 W BLB) located inside a black acrylic dome. The lamps emitted light at an intensity of 10.3 W·m −2 , which was measured with a Delta Ohm HD 2102.2 Photoradiometer using the filter for UV-A light range (k = 360 nm) at 5 mm [14]. The growth inhibition capacity of the bacteria in the materials was studied using E. coli, S. aureus, and P. aeruginosa bacteria. The tests were performed in two stages. The first stage followed the standard to evaluate the bactericidal capacity with the bacteria to be tested in the GP (with 10 wt.% TiO 2 ) and mGP (with 5 wt.% CuO) samples. This initial stage was performed by following the bacterial growth inhibition zone method (disc diffusion agar test). This method consisted of placing the sample, i.e., the GP and mGP disc, in a Petri dish and spreading nutrient agar on the sample. The Petri dishes were then covered for 24 h at 25 • C, and the bacterial growth was verified by the formation of an "inhibition halo" around the disc and under the disc. If the material is favorable to bacterial proliferation, more bacteria would be found at the site where the material rests ( Figure 3). Nottingham, UK) equipped with a rhodium tube with a maximum output of 4.0 kW and 0.02% sensitivity.  The X-ray diffraction (XRD) patterns were obtained with a RINT2000 wide-angle goniometer using Cu K radiation at 45 kV and 40 mA, and data were collected with a step size of 0.02° over the range of 5°-60° 2 using a scan speed of 5°/min.  Fourier-transform infrared spectroscopy (FTIR) was performed with a PerkinElmer Spectrum 100 spectrometer operated in transmittance mode, and data were collected for a wavelength range of 450 cm −1 to 4000 cm −1 . The samples were prepared using the compressed KBr method.  The morphological observations and particle sizes of TiO2 and CuO were evaluated by scanning electron microscopy (SEM) using a JEOL JSM-6490 LV SEM system operated with an accelerating voltage of 20 kV. The specimens were coated with gold, and the observations were made in vacuum mode.  The density, pore volume, and water absorption of the geopolymers were determined following the procedures detailed in the ASTM C642-13 standard, except that the temperature used to dry the sample in the oven was 60 °C for 48 h.

Evaluation of the Antibacterial Activity of the Geopolymeric Materials
The geopolymer samples were exposed to the bacteria under study by activating the materials with UV-A light for 48 h. The UV-A radiation was provided by two mercury lamps (Electrolux T8 20 W BLB) located inside a black acrylic dome. The lamps emitted light at an intensity of 10.3 W•m −2 , which was measured with a Delta Ohm HD 2102.2 Photoradiometer using the filter for UV-A light range (k = 360 nm) at 5 mm [14]. The growth inhibition capacity of the bacteria in the materials was studied using E. coli, S. aureus, and P. aeruginosa bacteria. The tests were performed in two stages. The first stage followed the standard to evaluate the bactericidal capacity with the bacteria to be tested in the GP (with 10 wt.% TiO2) and mGP (with 5 wt.% CuO) samples. This initial stage was performed by following the bacterial growth inhibition zone method (disc diffusion agar test). This method consisted of placing the sample, i.e., the GP and mGP disc, in a Petri dish and spreading nutrient agar on the sample. The Petri dishes were then covered for 24 h at 25 °C, and the bacterial growth was verified by the formation of an "inhibition halo" around the disc and under the disc. If the material is favorable to bacterial proliferation, more bacteria would be found at the site where the material rests ( Figure 3). By considering the results of the initial stage, the ability of the geopolymer paste (GP) and the mortar with glass (GP-G) to inhibit bacterial growth was evaluated in the second stage. During this stage, the methodology used was based on the Hasmaliza study [9], with a few modifications. The bacteria were cultured in tryptic soya broth (Merck, Darmstadt, Germany) for 24 h. At the beginning of the test, a count was performed in each of the broths by performing six serial dilutions in plate  By considering the results of the initial stage, the ability of the geopolymer paste (GP) and the mortar with glass (GP-G) to inhibit bacterial growth was evaluated in the second stage. During this stage, the methodology used was based on the Hasmaliza study [9], with a few modifications. The bacteria were cultured in tryptic soya broth (Merck, Darmstadt, Germany) for 24 h. At the beginning of the test, a count was performed in each of the broths by performing six serial dilutions in plate count agar (PCA, Scharlau 01-161). Subsequently, 100 µL of each of the selected bacteria were placed on discs, which were exposed for 2 to 24 h at room temperature (25 • C) under conditions isolated from contamination. After each of the exposure times, the discs were washed with 5 mL of a 1% peptone-buffered saline solution (Difco, Waltham, MA, USA), which was performed with vigorous stirring for 5 min; finally, the six dilutions were performed in a type-2 laminar flow cabinet (C4, Colombia) to count the number of colony-forming bacteria using the pour plate procedure with PCA. Finally, each agar with its respective inoculum was left in the incubator (WTC Binder, Germany) for 24 h at 37 • C to subsequently count the bacteria grown for each material in the different dilutions.

Physicochemical and Microstructural Characterization of the Starting Materials and the Produced Geopolymers
The chemical composition of MK and G is shown in Table 2. MK was basically composed of silica and alumina oxides (approximately 97 wt.%) and contains TiO 2 impurities (1.73 wt.%). This oxide was in the form of anatase, as seen in the XRD results ( Figure 4). The results shown in Table 2 indicate that the glass waste used in G was from the SiO 2 -Na 2 O-CaO system (calcium sodium glass) and was highly amorphous, as corroborated by the XRD results based on the elevation of the baseline for 2θ angles between 20 • and 30 • (Figure 4). count agar (PCA, Scharlau 01-161). Subsequently, 100 μL of each of the selected bacteria were placed on discs, which were exposed for 2 to 24 h at room temperature (25 °C) under conditions isolated from contamination. After each of the exposure times, the discs were washed with 5 mL of a 1% peptone-buffered saline solution (Difco, Waltham, Massachusetts, USA), which was performed with vigorous stirring for 5 min; finally, the six dilutions were performed in a type-2 laminar flow cabinet (C4, Colombia) to count the number of colony-forming bacteria using the pour plate procedure with PCA. Finally, each agar with its respective inoculum was left in the incubator (WTC Binder, Germany) for 24 h at 37 °C to subsequently count the bacteria grown for each material in the different dilutions.

Physicochemical and Microstructural Characterization of the Starting Materials and the Produced Geopolymers
The chemical composition of MK and G is shown in Table 2. MK was basically composed of silica and alumina oxides (approximately 97 wt.%) and contains TiO2 impurities (1.73 wt.%). This oxide was in the form of anatase, as seen in the XRD results ( Figure 4). The results shown in Table 2 indicate that the glass waste used in G was from the SiO2-Na2O-CaO system (calcium sodium glass) and was highly amorphous, as corroborated by the XRD results based on the elevation of the baseline for 2 angles between 20° and 30° ( Figure 4).    Titanium oxide existed in the anatase phase (TiO 2 , Inorganic Crystal Structure Database ICSD # 154604), as identified by the peaks observed in the diffractogram (Figure 4) at approximately 2θ = 25.3 • , 37.8 • , 48.1 • , 53.9 • , and 55.1 • , which also indicated the high photocatalytic potential of TiO 2 . The XRD pattern of the copper oxide nanoparticles synthesized from copper acetate by the Pechini method showed peaks at 2θ = 34 • , 36 • , 38 • , 49 • , 53 • , and 58 • , which corresponded to pure monoclinic CuO (ICSD code 67850), a phase considered to have bactericidal properties [42]. Similar results were found by Román et al. [15]. The XRD pattern obtained for the GP indicated that the material was amorphous (see the lifted baseline for 2θ between 25 • and 35 • ), with the only crystalline phase being the anatase phase, which was contributed to a high degree by the TiO 2 particles and to a lesser extent by MK.
SEM was used to determine the particle size of the TiO 2 and CuO particles ( Figure 5); the average TiO 2 and CuO particle sizes were 0.615 µm and 0.198 µm, respectively. Figure 5a shows the elongated and irregular shape of the TiO 2 particles, while Figure 5b shows that the CuO particles has a rounded and more homogeneous shape. 25.3°, 37.8°, 48.1°, 53.9°, and 55.1°, which also indicated the high photocatalytic potential of TiO2. The XRD pattern of the copper oxide nanoparticles synthesized from copper acetate by the Pechini method showed peaks at 2 = 34°, 36°, 38°, 49°, 53°, and 58°, which corresponded to pure monoclinic CuO (ICSD code 67850), a phase considered to have bactericidal properties [42]. Similar results were found by Román et al. [15]. The XRD pattern obtained for the GP indicated that the material was amorphous (see the lifted baseline for 2 between 25° and 35°), with the only crystalline phase being the anatase phase, which was contributed to a high degree by the TiO2 particles and to a lesser extent by MK. SEM was used to determine the particle size of the TiO2 and CuO particles ( Figure 5); the average TiO2 and CuO particle sizes were 0.615 μm and 0.198 μm, respectively. Figure 5a shows the elongated and irregular shape of the TiO2 particles, while Figure 5b shows that the CuO particles has a rounded and more homogeneous shape. The FTIR results obtained for MK, GP, and GP-G are shown in Figure 6. In the MK spectrum, a large band corresponding to asymmetric vibrations, specifically, vibrations of the Si-O-Si and O-Si-O groups, was centered at 1089 cm −1 [43]. The band located at 814 cm −1 was associated with the vibrational mode of the Al-O bond of the Al IV present in MK [43,44].
When MK was activated under alkaline conditions to form a geopolymer, the main bands at wavenumbers of 1007 and 1015 cm −1 shifted in both the GP and GP-G mortar spectra; this band corresponded to the asymmetric vibration of the Si-OT bonds in the GP gel potassium aluminum silicate hydrates (KASH) (where T corresponds to Si or Al tetrahedrons) [45]. According to Tchakouté et al. [46], the infrared absorption bands at wavenumbers close to 1100 cm −1 and 950 cm −1 could indicate that the geopolymers contained more SiQ 3 and SiQ 2 species, respectively. Additionally, the band observed in the GP-G mortar spectrum was more intense than that observed in the GP spectrum, indicating the presence of more undissolved silica in the alkaline system [43]. This result was expected, since the mortar was designed with particles of G. The band located at approximately 703 cm −1 came from symmetric vibrations of the presence of Ti-O-Ti photoactive species [10].
The peaks at approximately 3434 cm −1 and 1645 cm −1 in the MK, GP, and GP-G spectra corresponded to stress vibrations of the H-OH group, indicating that water molecules were associated with free water [38,[47][48][49]. Finally, the peaks corresponding to the bending vibration of the Si-O-Si group [47,49] were identifiable at 473, 463, and 470 cm −1 for the MK, GP, and GP-G samples, respectively.
The SEM images of GP and GP-G are shown in Figure 7. Figure 7a shows that the GP had a smooth and homogeneous surface, indicating the presence of large amounts of the KASH gel. The FTIR results obtained for MK, GP, and GP-G are shown in Figure 6. In the MK spectrum, a large band corresponding to asymmetric vibrations, specifically, vibrations of the Si-O-Si and O-Si-O groups, was centered at 1089 cm −1 [43]. The band located at 814 cm −1 was associated with the vibrational mode of the Al-O bond of the Al IV present in MK [43,44].
When MK was activated under alkaline conditions to form a geopolymer, the main bands at wavenumbers of 1007 and 1015 cm −1 shifted in both the GP and GP-G mortar spectra; this band corresponded to the asymmetric vibration of the Si-OT bonds in the GP gel potassium aluminum silicate hydrates (KASH) (where T corresponds to Si or Al tetrahedrons) [45]. According to Tchakouté et al. [46], the infrared absorption bands at wavenumbers close to 1100 cm −1 and 950 cm −1 could indicate that the geopolymers contained more SiQ 3 and SiQ 2 species, respectively. Additionally, the band observed in the GP-G mortar spectrum was more intense than that observed in the GP spectrum, indicating the presence of more undissolved silica in the alkaline system [43]. This result was expected, since the mortar was designed with particles of G. The band located at approximately 703 cm −1 came from symmetric vibrations of the presence of Ti-O-Ti photoactive species [10]. investigated, and it was noteworthy that there was no significant difference between the morphologies of the systems with and without TiO2, and that the formation of the KASH gel was not impeded by the addition of TiO2, as these coexisted in the structure of the material. Comparing the physical properties (Table 3) of the geopolymer matrix [11], with and without TiO2 addition, we found that the water absorption decreased by just 3.9%, and the density and volume of the permeable pores increased by 5.73% and 1.52%, respectively.  The glass particles of the GP-G mortar (Figure 7b) were identifiable by their large sizes and angular smooth surfaces [41,47], which were due to the milling processes that these particles underwent. The presence of micro-cracks in the sample was also observed with the incorporation of glass ( Figure 7b); similar results were reported by Lin et al. [47] and Mejía de Gutiérrez et al. [41]. The GP-G had a more homogeneous and denser surface similar to that reported by Lin et al. [47] and a higher density (see Table 3); the material was more compact, which was reflected in its lower water absorption capacity and lower volume of permeable pores.  The peaks at approximately 3434 cm −1 and 1645 cm −1 in the MK, GP, and GP-G spectra corresponded to stress vibrations of the H-OH group, indicating that water molecules were associated with free water [38,[47][48][49]. Finally, the peaks corresponding to the bending vibration of the Si-O-Si group [47,49] were identifiable at 473, 463, and 470 cm −1 for the MK, GP, and GP-G samples, respectively.
The SEM images of GP and GP-G are shown in Figure 7. Figure 7a shows that the GP had a smooth and homogeneous surface, indicating the presence of large amounts of the KASH gel. Unreacted MK that was not dissolved by the alkaline activation conditions was also identified [11,44,47]. GP showed a homogeneous distribution of the TiO 2 nanoparticles inside the matrix. In a previous study [11], the effect of the incorporation of TiO 2 in the geopolymeric matrix was investigated, and it was noteworthy that there was no significant difference between the morphologies of the systems with and without TiO 2 , and that the formation of the KASH gel was not impeded by the addition of TiO 2 , as these coexisted in the structure of the material. Comparing the physical properties (Table 3) of the geopolymer matrix [11], with and without TiO 2 addition, we found that the water absorption decreased by just 3.9%, and the density and volume of the permeable pores increased by 5.73% and 1.52%, respectively. investigated, and it was noteworthy that there was no significant difference between the morphologies of the systems with and without TiO2, and that the formation of the KASH gel was not impeded by the addition of TiO2, as these coexisted in the structure of the material. Comparing the physical properties (Table 3) of the geopolymer matrix [11], with and without TiO2 addition, we found that the water absorption decreased by just 3.9%, and the density and volume of the permeable pores increased by 5.73% and 1.52%, respectively.  The glass particles of the GP-G mortar (Figure 7b) were identifiable by their large sizes and angular smooth surfaces [41,47], which were due to the milling processes that these particles underwent. The presence of micro-cracks in the sample was also observed with the incorporation of glass (Figure 7b); similar results were reported by Lin et al. [47] and Mejía de Gutiérrez et al. [41]. The GP-G had a more homogeneous and denser surface similar to that reported by Lin et al. [47] and a higher density (see Table 3); the material was more compact, which was reflected in its lower water absorption capacity and lower volume of permeable pores. The glass particles of the GP-G mortar (Figure 7b) were identifiable by their large sizes and angular smooth surfaces [41,47], which were due to the milling processes that these particles underwent. The presence of micro-cracks in the sample was also observed with the incorporation of glass ( Figure 7b); similar results were reported by Lin et al. [47] and Mejía de Gutiérrez et al. [41]. The GP-G had a more homogeneous and denser surface similar to that reported by Lin et al. [47] and a higher density (see Table 3); the material was more compact, which was reflected in its lower water absorption capacity and lower volume of permeable pores. Table 3. Physical properties of the GP and GP-G samples.

Sample
Paste without TiO 2 [11] GP (Paste) ( Figure 8 shows the results of the first experimentation stage, corresponding to the standardization method using Petri dishes and exposure in nutrient agar with the GP and mGP. As shown in Figure 8a, for the mGP, no inhibition halo was observed for E. coli. Although authors such as Román et al. [15] showed the capacity of CuO nanoparticles to eliminate Ochrobactrum anthropi, in the present study and under the composition used (5 wt.% CuO), CuO geopolymeric compounds with antibacterial capacity for E. coli, S. aureus, and P. aeruginosa were not obtained.  Figure 8 shows the results of the first experimentation stage, corresponding to the standardization method using Petri dishes and exposure in nutrient agar with the GP and mGP. As shown in Figure 8a, for the mGP, no inhibition halo was observed for E. coli. Although authors such as Román et al. [15] showed the capacity of CuO nanoparticles to eliminate Ochrobactrum anthropi, in the present study and under the composition used (5 wt.% CuO), CuO geopolymeric compounds with antibacterial capacity for E. coli, S. aureus, and P. aeruginosa were not obtained.

Assays with Bacteria
Previous studies demonstrated that the quantity of nanoparticles is an important parameter. The entrapment and inhibition of bacteria on surfaces was evaluated using CuO and Ag nanoparticles [2,22,33,34,42], and a good compatibility was reported in orthodontic adhesives using CuO in high quantities [17]. The amount of CuO nanoparticles used in this preliminary study was probably low and, for this reason, it did not allow for bacterial elimination. This is according to Guo et al. [14], who evaluated different percentages of TiO2 in coatings fabricated by immersion and reported that an incorporation of 5 wt.% TiO2 particles failed to eliminate E. coli, which was attributed to the processes of initial photocatalytic inactivation step being slow with this proportion of titanium oxide.
These nanoparticles were incorporated into materials because of their high surface/volume ratio, which allowed interactions with bacterial cell membranes, preventing these microorganisms from attaching to the material surface (bacteriostatic effect); when this occurred, the material was able to eliminate these microorganisms (bactericidal effect) [13,[22][23][24]34]. Table 4 shows the results of the initial standardization assay for GP and mGP with the three bacteria tested.  In the case of the geopolymer with TiO2 nanoparticles (GP), the standardization results were satisfactory for E. coli, in which a bactericidal effect was in fact observed for the sample GP. The inhibition was satisfactory, and a halo did form around the sample (Figure 8a); additionally, when sample GP was removed from the agar nutrient, no bacteria were found under the sample, as shown Previous studies demonstrated that the quantity of nanoparticles is an important parameter. The entrapment and inhibition of bacteria on surfaces was evaluated using CuO and Ag nanoparticles [2,22,33,34,42], and a good compatibility was reported in orthodontic adhesives using CuO in high quantities [17]. The amount of CuO nanoparticles used in this preliminary study was probably low and, for this reason, it did not allow for bacterial elimination. This is according to Guo et al. [14], who evaluated different percentages of TiO 2 in coatings fabricated by immersion and reported that an incorporation of 5 wt.% TiO 2 particles failed to eliminate E. coli, which was attributed to the processes of initial photocatalytic inactivation step being slow with this proportion of titanium oxide.
These nanoparticles were incorporated into materials because of their high surface/volume ratio, which allowed interactions with bacterial cell membranes, preventing these microorganisms from attaching to the material surface (bacteriostatic effect); when this occurred, the material was able to eliminate these microorganisms (bactericidal effect) [13,[22][23][24]34]. Table 4 shows the results of the initial standardization assay for GP and mGP with the three bacteria tested. In the case of the geopolymer with TiO 2 nanoparticles (GP), the standardization results were satisfactory for E. coli, in which a bactericidal effect was in fact observed for the sample GP. The inhibition was satisfactory, and a halo did form around the sample ( Figure 8a); additionally, when sample GP was removed from the agar nutrient, no bacteria were found under the sample, as shown in Figure 8b. On the contrary, for the mGP, the halo formation was not evidenced; when the mGP sample was removed from the agar nutrient, an appreciable number of colonies grew below it for the three bacteria tested.
Based on the preliminary results of the first phase of standardization, the study was continued exclusively with GP samples; additionally, a GP-G mortar was fabricated and tested. The decision to use a geopolymer mortar with glass to measure the bactericide capacity of the geopolymers was based on the results reported by Mejía de Gutiérrez et al. [41], who observed a higher photocatalytic efficiency for B-rhodamine degradation in compounds functionalized with TiO 2 when glass waste was used to prepare the geopolymer mortars. Likewise, studies by Sikora et al. [35] showed that the use of glass enhanced the photocatalytic activity for E. coli colony degradation, and elimination occurred in 30 min.
In the second phase, the number of CFUs was analyzed in different solutions for short times (4-5 h) and after one day in the agar with the E. coli, P. aeruginosa, and S. aureus bacteria.
Analyzing the GP-G mortar exposed to the different solutions for short times (Table 5) showed that, after 5 h, CFUs were not present the in the 10 −7 mL solutions for the three bacteria evaluated. Evaluating S. aureus exposed to GP (Figure 9) for 4 h in all solutions showed CFU growth, while, for the GP-G in the 10 −7 solutions, zero CFUs were evident. However, the GP exhibited significant antimicrobial activity for only the 10 −7 solutions containing P. aeruginosa (Figure 9). The results reported in this study corresponding to GP and GP-G are satisfactory. The toxicity of nanoparticles for inhibiting bacterial growth was previously demonstrated for S. aureus using ZnO nanoparticles by Sikora [35], and for E. coli using CuO by Kumar [20] and TiO 2 by Sunada et al. [50]. Sunada et al. [50] explained that the photokilling reaction of E. coli cells using TiO 2 is initiated by a partial decomposition of the outer membrane, followed by an attack of the cytoplasmic membrane, resulting in cell death. In general, the adhesion of nanoparticles onto the cell wall and the membrane of the microorganisms produces morphological changes characterized by shrinkage of the cytoplasm and membrane detachment, finally leading to rupture of cell wall [51]. Additionally, the photocatalysis generates reactive oxygen species (ROS) and free radical species, contributing to an increase in the antibacterial potential of the nanoparticles [34,51,52].
For the agar solutions exposed to GP for longer times (Table 6), the greatest inhibition occurred in the 10 −6 solutions for Pseudomonas aeruginosa ( Figure 10) and E. coli (Figure 11). The highest efficacy for the inhibition of CFU bacterial growth was evidenced by the GP-G mortar in the 10 −6 solutions for the three bacteria evaluated. This result confirms that the incorporation of glass wastes in geopolymeric compounds increased the photocatalytic capacity and the bactericidal effect of the MK-based geopolymer supplemented with TiO 2 and, therefore, improved the bacterial growth inhibition capacity on surfaces.
Finally, according to Tables 5 and 6, samples GP and GP-G showed a bacteriostatic effect depending on the bacteria and time.
Although TiO 2 and other nanoparticles previously attracted a lot of interest due to their antibacterial properties in different applications, according to the results, in general, samples containing glass wastes showed a higher bacteriostatic effect. The use of ground glass particles maximized the capacity for inhibiting CFU growth after 5 h for the GP-G mortars in solutions of 10 −7 mL containing the three bacteria evaluated (S. aureus, P. aeruginosa, and E. coli). Furthermore, GP-G seems to be particularly effective against P. aeruginosa.    the three bacteria evaluated. This result confirms that the incorporation of glass wastes in geopolymeric compounds increased the photocatalytic capacity and the bactericidal effect of the MKbased geopolymer supplemented with TiO2 and, therefore, improved the bacterial growth inhibition capacity on surfaces.       Finally, according to Tables 5 and 6, samples GP and GP-G showed a bacteriostatic effect depending on the bacteria and time.
Although TiO2 and other nanoparticles previously attracted a lot of interest due to their antibacterial properties in different applications, according to the results, in general, samples containing glass wastes showed a higher bacteriostatic effect. The use of ground glass particles maximized the capacity for inhibiting CFU growth after 5 h for the GP-G mortars in solutions of 10 −7 mL containing the three bacteria evaluated (S. aureus, P. aeruginosa, and E. coli). Furthermore, GP-G seems to be particularly effective against P. aeruginosa.

Conclusions
Geopolymer composites based on the alkaline activation of MK and nanoparticles of TiO2 (10

Conclusions
Geopolymer composites based on the alkaline activation of MK and nanoparticles of TiO 2 (10 wt.%) and CuO (5 wt.%) were produced. This study evaluated the physical and microstructural properties of the geopolymers and the functionality of these geopolymers for inhibiting the growth of the bacteria S. aureus, P. aeruginosa, and E. coli. Based on the results obtained, the following conclusions can be drawn:

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Here, 10 wt.% TiO 2 used for the manufacture of geopolymeric pastes and mortars showed satisfactory elimination of bacterial growth. In contrast, 5 wt.% CuO did not inhibit bacterial growth.

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The incorporation of glass wastes as fine aggregate endowed the GP-G with a 56.73% lower water absorption compared to the GP sample. Likewise, the glass particles endowed the material with a smoother and more homogeneous surface, 40.36% higher density, and 37.97% lower pore volume.

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The use of ground glass particles maximized the capacity for inhibiting CFU growth after 5 h for the GP-G mortars in solutions of 10 −7 mL containing the three bacteria evaluated (S. aureus, P. aeruginosa, and E. coli).

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After 24 h in the bacterial culture, the GP-G mortars exhibited a high capacity for inhibiting the growth of P. aeruginosa in the 10 −4 mL solutions and E. coli and S. aureus in the 10 −6 mL solutions.

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These results indicate the potential for using the MK-based geopolymer composite with 10 wt.% TiO 2 for applications on surfaces with antibacterial properties.