A Circular Economy Virtuous Example—Use of a Stabilized Waste Material Instead of Calcite to Produce Sustainable Composites

: This work reports and analyzes the mechanical properties of some composites obtained using stabilized waste with epoxy resins E-227. For comparison, correspondent composite samples were realized using calcite as a ﬁller. The recovered stabilized waste was obtained by means of a new method to stabilize municipal solid waste incineration (MSWI) ﬂy ash (FA), based on the use of bottom ash (BA). The aim of this paper is to show that the stabilization process, which can be considered a zero—waste treatment, produces inert materials, that can be reused as a ﬁller. The production of new ﬁller was made on a pilot plant, designed to verify the transferability of the proposed stabilization technology. Mechanical analysis revealed that ﬂexural modulus raises by increasing the ﬁller content around 30% wt, independently of ﬁller type, stabilized sample or calcium carbonate. Mechanical properties are lower in the samples with the high amount of ﬁller due to the crowding e ﬀ ect. The morphology of composite materials showed a non-homogeneous dispersion of particles in stabilized sample ﬁller, characterized by large particle agglomerates. Finally, according to the ESCAPE simpliﬁed method, the obtained composites result more sustainable in comparison with the corresponding ones produced by using natural resources (like calcite). These ﬁndings open new possibilities for the reuse of the stabilized material, in frame of circular economy principles, with environmental and economic advantages.


Introduction
Incineration is an effective method to manage municipal solid wastes (MSW). Indeed, the waste volume is reduced up to 90%, with the by-product to concentrate persistent pollutants in combustion residues. According to European Union waste management strategy, the use of bottom ash (BA) is generally suggested as a sustainable solution to manage this secondary waste [1]. Indeed, MSW incineration BA is ever more identified as a potential source for materials of great importance to the economy [2]. BA was been proposed to be reused, for example, in building industry [3]. Incorporation of BA has already been demonstrated by Nikravan et al. for the partial substitution of aggregate and

Materials and Methods
In this study, Coal Fly Ash (CFA), Flue Gas Desulphurization (FGD), FA and BA were considered. CFA is produced as a by-product in thermal power plant during coal combustion. Fly ashes, classified as fine particulate residues, were removed from the combustion gases before they are emitted into the atmosphere by a dust-collection system [27]. FGD residues are another by-product resulting from coal combustion processes in power plants. In this process, insoluble calcium sulphite and calcium sulphate solids are formed due to the use of a lime-based or a sodium-based reagent [28].
In the present work, CFA and FGD residues were collected at the pulverized coal thermal power plant located in Brescia, Italy. BA and FA were provided by the Brescia (Italy) municipal solid waste incinerator plant. The latter works with three combustion lines per day, with a capacity of 880 tons MSW ashes each. For years, co-combustion of municipal solid waste with sewage sludge has been applied at this incineration plant. Large particles were separated from BA before their use. Afterwards, a milling procedure was applied to BA portion in order to obtain particles less than 700 µm.
The flue gas cleaning system involves the uses of dry scrubbers, fabric filters, an activated carbon injection system and a combination selective non-catalytic and catalytic reductions. Moreover, the plant contains a device installed to monitor the continuous flue gas emissions.
An industrial grade calcium carbonate (CaCO 3 ) Calcite V40 (Carrara, Italy), with a particle diameter distribution below 60 µm (99%), was used as a reference to produce polymer filler composites. The composite material matrix consists of Epoxy resin E-227 (produced by Prochima), also known as polyepoxides. This is a class of reactive pre-polymers and polymers characterized by the presence of epoxide groups. The bi-component product is formed by polymer and catalyst that must be mixed according to the ratio indicated by the manufacture equal to 1/2 in weight to obtain the final product.

Stabilization Procedure on the Pilot Plant
FA was stabilized by using the pilot plant (see Figure 1) placed in a Brescia incinerator, as described by Benassi et al. [13]. FGD and CFA were mixed with FA with relative weight percentage fixed at 65% FA, 20% FGD and 15% CFA. Calcium sulfite hydrate and portlandite are identified as the main crystalline phases of FGD residues. CFA revealed only two crystalline phases:-quartz and mullite [29]. In this study, the sample was prepared by mixing FA, CFA, FGD and BA, as reported by Assi et al. [21]. Tap water (25 kg) at room temperature was also used. The mixing procedure was made for 30 min as reported by Benassi et al. [13]. After the synthesis, the material underwent a natural aging process at the incinerator plant for 11 months, in order to promote carbonation reactions, that contribute to the stabilization of heavy metals over time as already discussed by Assi et al. [19]. The sample stability was verified by performing leaching tests on the stabilized product at 1, 2, 3 and 11 months after the treatment.
Appl. Sci. 2020, 10, x FOR PEER REVIEW 3 of 15 Afterwards, a milling procedure was applied to BA portion in order to obtain particles less than 700 µm. The flue gas cleaning system involves the uses of dry scrubbers, fabric filters, an activated carbon injection system and a combination selective non-catalytic and catalytic reductions. Moreover, the plant contains a device installed to monitor the continuous flue gas emissions.
An industrial grade calcium carbonate (CaCO3) Calcite V40 (Carrara, Italy), with a particle diameter distribution below 60 µm (99%), was used as a reference to produce polymer filler composites. The composite material matrix consists of Epoxy resin E-227 (produced by Prochima), also known as polyepoxides. This is a class of reactive pre-polymers and polymers characterized by the presence of epoxide groups. The bi-component product is formed by polymer and catalyst that must be mixed according to the ratio indicated by the manufacture equal to 1/2 in weight to obtain the final product.

Stabilization Procedure on the Pilot Plant
FA was stabilized by using the pilot plant (see Figure 1) placed in a Brescia incinerator, as described by Benassi et al. [13]. FGD and CFA were mixed with FA with relative weight percentage fixed at 65% FA, 20% FGD and 15% CFA. Calcium sulfite hydrate and portlandite are identified as the main crystalline phases of FGD residues. CFA revealed only two crystalline phases:-quartz and mullite [29]. In this study, the sample was prepared by mixing FA, CFA, FGD and BA, as reported by Assi et al. [21]. Tap water (25 kg) at room temperature was also used. The mixing procedure was made for 30 min as reported by Benassi et al. [13]. After the synthesis, the material underwent a natural aging process at the incinerator plant for 11 months, in order to promote carbonation reactions, that contribute to the stabilization of heavy metals over time as already discussed by Assi et al. [19]. The sample stability was verified by performing leaching tests on the stabilized product at 1, 2, 3 and 11 months after the treatment.

Preparation of Composite Samples
Calcite and stabilized sample were used as filler. A series of five specimens:-0%, 10%, 30%, 50% and 70% wt were prepared by mixing the epoxy resin with calcite or stabilized sample in a beaker for about 5 min. After that, the mixture was drained in a mold and maintained for 24 h at room temperature to obtain a sufficient hardness. The samples of epoxy composites with different filler were fabricated according to the following steps:-(i) silicone rubber molds have been produced in order to realize the negative shape of the samples;-(ii) the stabilized sample has been mixed with the epoxy resin before pouring the mix in the molds; (iii) material stand-by for 4 days at room

Preparation of Composite Samples
Calcite and stabilized sample were used as filler. A series of five specimens:-0%, 10%, 30%, 50% and 70% wt were prepared by mixing the epoxy resin with calcite or stabilized sample in a beaker for about 5 min. After that, the mixture was drained in a mold and maintained for 24 h at room temperature to obtain a sufficient hardness. The samples of epoxy composites with different filler were fabricated according to the following steps:-(i) silicone rubber molds have been produced in order to realize the negative shape of the samples;-(ii) the stabilized sample has been mixed with the epoxy resin before pouring the mix in the molds; (iii) material stand-by for 4 days at room temperature. The same procedure has been applied to prepare the specimens with calcite as a filler. Figure 2 shows the two different samples prepared with stabilized FA and calcite, respectively.
Appl. Sci. 2020, 10, x FOR PEER REVIEW 4 of 15 temperature. The same procedure has been applied to prepare the specimens with calcite as a filler. Figure 2 shows the two different samples prepared with stabilized FA and calcite, respectively.

Leaching Tests
Leaching test was performed to raw powders and stabilized sample according the CEN normative (CEN EN 12457-2) [30] and optimized procedure [14,21]. For leaching tests, 20 g of each sample were mixed with 200 mL MQ water (1:10) and mixed at room temperature for 2 h by a magnetic stirrer. After that, samples were filtered through 0.45 µm pore membranes and the pH of the filtrates was checked by pH-meter (Metrohm, model 827 Lab, Origgio, Italy). The analyses of leaching solutions were scheduled at one (1 M), two (2 M), three (3 M) and eleven months (11 M) after the stabilization, in order to investigate the efficacy of the process.
Elemental chemical analysis of the leachate solutions was performed by means of Total reflection X-Ray Fluorescence (TXRF) technique. The S2 Picofox system from Bruker (Bruker AXS Microanalysis GmbH, Berlin, Germany), equipped with a Mo tube operating at 50 kV and 750 µA and a Silicon Drift Detector (SDD), was employed. Internal standard method is used to calculate the selected analytes concentration. To this aim, a stock solution of 1 g/L Ga in nitric acid (Ga-ICP Standard Solution, Fluka, Sigma Aldrich, Saint Louis, MO, USA) was used. A solution with final concentration of 1 mg/L of Ga was obtained by adding about 10 µL of a solution of 100 mg/L of Ga to 1 mL solution. In order to obtain homogenized working solutions, a vortex shaker at 2500 rpm was employed for 1 min. A droplet of 10 µL was deposited onto the surface of an acrylic reflector in a central position. Before measurements, the reflectors were left dried under a laminar hood on a hot plate at 50 °C and the residues were measured. For each sample, three independent reflectors were prepared and irradiated for 600 s of live time. All the recorded TXRF spectra were analyzed with the instrumental software. In these experimental conditions, P, S and Cl are low Z elements such as P, S and Cl that are underestimated [31]. For this reason, the quantification of these elements was corrected using the calculated relative sensitivities for P and S obtained by the calibration curves [32].

XRD
X-ray diffraction (XRD) is performed for structural and microstructural characterization of the raw powders [21] and the stabilized sample after 11 M (see Figure 3). XRD patterns were acquired by means of an X'Pert PRO Bragg Brentano diffractometer (Malvern PANalytical, UK) equipped with a Cu K anode and operating at 40 kV and a current of 40 mA. Scans (2θ) were performed from 5° to 90°, with a step interval of 0.0167°. Philips X'Pert software (associated with the COD open database) was employed for phase identification.

Leaching Tests
Leaching test was performed to raw powders and stabilized sample according the CEN normative (CEN EN 12457-2) [30] and optimized procedure [14,21]. For leaching tests, 20 g of each sample were mixed with 200 mL MQ water (1:10) and mixed at room temperature for 2 h by a magnetic stirrer. After that, samples were filtered through 0.45 µm pore membranes and the pH of the filtrates was checked by pH-meter (Metrohm, model 827 Lab, Origgio, Italy). The analyses of leaching solutions were scheduled at one (1 M), two (2 M), three (3 M) and eleven months (11 M) after the stabilization, in order to investigate the efficacy of the process.
Elemental chemical analysis of the leachate solutions was performed by means of Total reflection X-Ray Fluorescence (TXRF) technique. The S2 Picofox system from Bruker (Bruker AXS Microanalysis GmbH, Berlin, Germany), equipped with a Mo tube operating at 50 kV and 750 µA and a Silicon Drift Detector (SDD), was employed. Internal standard method is used to calculate the selected analytes concentration. To this aim, a stock solution of 1 g/L Ga in nitric acid (Ga-ICP Standard Solution, Fluka, Sigma Aldrich, Saint Louis, MO, USA) was used. A solution with final concentration of 1 mg/L of Ga was obtained by adding about 10 µL of a solution of 100 mg/L of Ga to 1 mL solution. In order to obtain homogenized working solutions, a vortex shaker at 2500 rpm was employed for 1 min. A droplet of 10 µL was deposited onto the surface of an acrylic reflector in a central position. Before measurements, the reflectors were left dried under a laminar hood on a hot plate at 50 • C and the residues were measured. For each sample, three independent reflectors were prepared and irradiated for 600 s of live time. All the recorded TXRF spectra were analyzed with the instrumental software. In these experimental conditions, P, S and Cl are low Z elements such as P, S and Cl that are underestimated [31]. For this reason, the quantification of these elements was corrected using the calculated relative sensitivities for P and S obtained by the calibration curves [32].

XRD
X-ray diffraction (XRD) is performed for structural and microstructural characterization of the raw powders [21] and the stabilized sample after 11 M (see Figure 3). XRD patterns were acquired by means of an X'Pert PRO Bragg Brentano diffractometer (Malvern PANalytical, UK) equipped with a Cu K anode and operating at 40 kV and a current of 40 mA. Scans (2θ) were performed from 5 • to 90 • , with a step interval of 0.0167 • . Philips X'Pert software (associated with the COD open database) was employed for phase identification. Figure 3 reports the XRD pattern of the stabilized material 11 months after the synthesis procedure. The following crystalline phases are detected:-halite (NaCl), calcite (CaCO3), quartz (SiO2), hannebachite (Ca2H2O7S2), belite (Ca2SiO5), sylvine (KCl) and bassanite (Ca3H4O13.8S3).
where σ fmax is the flexural strength (MPa), P is the load (N), L is the support span (mm), b is the sample width (mm) and d is the sample thickness (mm).

SEM-EDXS
The morphology of the raw powders and obtained samples was characterized by a scanning electron microscope (SEM) Zeiss LEO EVO 40XVP (Carl Zeiss Microscopy GmbH, Oberkochen, Germany) equipped with a Link Analytical probe for energy dispersive X-ray spectroscopy (EDXS, Oxford Instruments NanoAnalysis, Buckinghamshire, UK). Gold was deposited on the sample surface in order to ensure the electrical charge. Secondary electron mode was employed to characterize the composites the morphology.

Evaluation of the Sustainability of the Proposed Technology
Recently, a rapid and suitable method to compare two materials, based on an index, was been introduced [7,34]. This approach is named ESACPE, standing for Evaluation of Sustainability of material substitution using carbon footprint by a simplified approach. This approach was proposed to support industrial transition to CE, by means of a method, based on the use of simplified indicators, for the evaluation of raw materials substitution sustainability.
An index (SUB-RAW index, see in the following) was introduced as a parameter to quantify the environmental benefices of a raw material substitution. It is evaluated only taking into account two parameters, strictly connected to the environmental performance of the considered materials, that are embodied energy (EE) and CO 2 footprint (CF).
The materials production from ores and feedstock requires energy, which is defined as "embodied energy." EE accounts for all direct and indirect energies needed for the production of 1 kg of a material [35]. The CO 2 footprint corresponds to the equivalent mass of greenhouse gases (kg CO 2 equivalent), produced and released into the atmosphere due to the production of 1 kg of the material [35].
In general, The EE and CF account for the resources and the emissions, respectively, involved in the synthesis of a material.
These parameters do not take into account functional and economical properties of the considered materials. Indeed, the basic idea of the proposed method is to use a simplified approach to evaluate material substitution. This is the reason the procedure must be simple and accessible to all.
Eventually after the positive results obtained by the ESCAPE method it would be possible to perform complete Life Cycle Assessment analysis, to globally evaluate the proposed material substitution.
The SUB-RAW index is defined as: where the subscripts raw and sub stand for raw material and new proposed material, respectively. The EE and CF range from 0.01 to 10 6 -10 7 , respectively reported in kg/kg and MJ/kg. Due to the large range of values, a logarithmic scale is often used. All the EE and CF parameters are used without their dimension, obtaining a dimensionless numerical value. It corresponds to a mean parameter accounting for environmental pressure and energies of the two materials, that are compared.
The goal to substitute natural resources with more sustainable materials is obtained when the index results positive. A positive value of this index, even if it is very low, can be a very good result in terms of substitution.
For example, a SUB-RAW index of about 0, 1, indeed, corresponds to a mean variation of EE and CF of about 25%.

TXRF Analysis
TXRF results of leachate solutions of raw ashes are reported in Table 1, with good agreement with previous studies [36][37][38]. The major elements in leachable FA are Cl, Ca and Br. Ca is also identified as the essential constituent of BA but its higher presence in FA is expected due to the addition of Ca(OH) 2 to adsorb acid gases (like SO 2 and HCl), produced during the incineration process. S is another element found in higher amount in FA with respect to BA due to the lower boiling points and higher volatility of the sulphate phases [38]. Other elements are found in trace amounts in all raw ashes. Zn and Pb show significant differences between FA and BA, in agreement with reported literature [13,38]. These two heavy metals are almost one order of magnitude higher in FA compared to BA and lower in CFA and FGD. As reported in Table 1, these ashes contain mostly Ca and S [14,39], while other elements are in low concentrations. Literature reports extremely high concentration of Si in CFA [27] but under this experimental conditions, Si could not be quantified.
Stabilized sample revealed a noticeable decrease in Pb and Zn leaching after the first month with respect to the raw FA. While, after 2 M, Pb concentration is lower than lower detection limit (LOD) by TXRF spectrometry (see Table 2), which is 0.002 mg/L [40]. In contrast, stabilized sample revealed higher S concentration compared with FA due to FGD residues addition for stabilization. Based on data reported in Table 2, we can conclude that the lower Zn and Pb leachability must be attributed to the carbonation and pozzolanic reactions that occur during stabilization [21]. It is already shown that pH is a key factor that affects heavy metals leaching behaviors. Considering the pH of all raw powders and final stabilized mixtures, it is extremely interesting to note that all ashes have a starting pH higher than 12 (see Table 1), while stabilized sample has a pH lower than 11 (see Table 2). In this way, pH monitoring also allows the following of the carbonation reactions [19].  In particular, the natural aging of stabilized material allows us to sequestrate carbon dioxide, making it possible to take advantage of the carbonation reaction, as a by-product of the stabilization mechanism [19]. Indeed, carbonation produces a pH neutralizing effect (the pH evolution of stabilized material, with time is reported in Table 2, which contributes to decrease the solubility/mobility of heavy metals. Figure 3 reports the XRD pattern of the stabilized material 11 months after the synthesis procedure. The following crystalline phases are detected:-halite (NaCl), calcite (CaCO 3 ), quartz (SiO 2 ), hannebachite (Ca 2 H 2 O 7 S 2 ), belite (Ca 2 SiO 5 ), sylvine (KCl) and bassanite (Ca 3 H 4 O 13.8 S 3 ).

XRD Pattern
The material is made of the same crystalline phases already detected in similar materials, stabilized by using amorphous silica sources [11,18], which are analyzed weeks after the treatment. The XRD spectra collected on stabilized material 1 month after the material synthesis (data not shown) corresponds to the one already reported by Assi et al. [21], due to the same stabilization procedure adopted. However, it is worth to notice the presence of belite in this sample. This phase was not found in previous works using the proposed stabilization methods [41] and is generally present as an additional main mineralogical component of calcium sulfoaluminate cement, which can be obtained by using FA [42]. Then its presence, although it was not expected, can be justified by previous works. It was already shown that FA and a source of lime (derived from FGD residues introduced in the sample stabilization procedure) respectively served as the principal raw silica and lime sources during the production of building materials such as clinker [43]. In the present case, the addition of BA allows us to increase the amount of CaO-Al 2 O 3 -SiO 2 able to increase the reactive amorphous phase that contribute to the heavy metals stabilization [44]. The belite formation is probably due to the crystallization of C-S-H (calcium silicate hydrate) phase, due to the reaction between silicate species and calcium, which in cement is a hydration product.
The stabilized material contains ceramic and silica-based material. This allows us to suppose that it may be reused to substitute some natural resources, with similar composition. One advantage of the obtained stabilized material is its physical form. Being a powder, it may be used as a filler in a composite, realized by mixing a matrix with a powder. In principle, this material may be used with all matrices requiring inorganic filler. In the present work, this filler was used to produce some composites by using an epoxy resin E-227, as described in the experimental section.

Three Point Bending Test
Flexural strength and modulus of elasticity were obtained through a three-point bending test. Figure 4 reports a stress-strain curves obtained at different content (50% and 70%) of calcium carbonate and stabilized sample (ash) in comparison with neat polymer. Flexural modulus, evaluated from the slope of the stress versus strain deflection curve determines how much a sample will bend when a given load is applied, while flexural strength is calculated as the maximum bending stress.
Appl. Sci. 2020, 10, x FOR PEER REVIEW 8 of 15 The material is made of the same crystalline phases already detected in similar materials, stabilized by using amorphous silica sources [11,18], which are analyzed weeks after the treatment. The XRD spectra collected on stabilized material 1 month after the material synthesis (data not shown) corresponds to the one already reported by Assi et al. [21], due to the same stabilization procedure adopted. However, it is worth to notice the presence of belite in this sample. This phase was not found in previous works using the proposed stabilization methods [41] and is generally present as an additional main mineralogical component of calcium sulfoaluminate cement, which can be obtained by using FA [42]. Then its presence, although it was not expected, can be justified by previous works. It was already shown that FA and a source of lime (derived from FGD residues introduced in the sample stabilization procedure) respectively served as the principal raw silica and lime sources during the production of building materials such as clinker [43]. In the present case, the addition of BA allows us to increase the amount of CaO-Al2O3-SiO2 able to increase the reactive amorphous phase that contribute to the heavy metals stabilization [44]. The belite formation is probably due to the crystallization of C-S-H (calcium silicate hydrate) phase, due to the reaction between silicate species and calcium, which in cement is a hydration product.
The stabilized material contains ceramic and silica-based material. This allows us to suppose that it may be reused to substitute some natural resources, with similar composition. One advantage of the obtained stabilized material is its physical form. Being a powder, it may be used as a filler in a composite, realized by mixing a matrix with a powder. In principle, this material may be used with all matrices requiring inorganic filler. In the present work, this filler was used to produce some composites by using an epoxy resin E-227, as described in the experimental section.

Three Point Bending Test
Flexural strength and modulus of elasticity were obtained through a three-point bending test. Figure 4 reports a stress-strain curves obtained at different content (50% and 70%) of calcium carbonate and stabilized sample (ash) in comparison with neat polymer. Flexural modulus, evaluated from the slope of the stress versus strain deflection curve determines how much a sample will bend when a given load is applied, while flexural strength is calculated as the maximum bending stress. In Figure 4, it is possible to notice first that the neat epoxy shows an elongation at break much higher than that both stabilized sample-epoxy and calcium carbonate-epoxy composites. Moreover, the neat epoxy did not break brittle but it yields above the peak. The presence of 50% by weight of filler significantly reduces the elongation at break of the composites and a major amount of filler up to 70% by weight further decreases it. The influence of stabilized FA as filler in epoxy resin matrix on the elongation at break is similar to that of calcium carbonate. As expected, increasing the filler amount in the epoxy matrix the elongation and the straight at break decrease, while the flexural modulus increases [45][46][47]. In general, the same content [% wt] of ash and calcium carbonate affects In Figure 4, it is possible to notice first that the neat epoxy shows an elongation at break much higher than that both stabilized sample-epoxy and calcium carbonate-epoxy composites. Moreover, the neat epoxy did not break brittle but it yields above the peak. The presence of 50% by weight of Appl. Sci. 2020, 10, 754 9 of 16 filler significantly reduces the elongation at break of the composites and a major amount of filler up to 70% by weight further decreases it. The influence of stabilized FA as filler in epoxy resin matrix on the elongation at break is similar to that of calcium carbonate. As expected, increasing the filler amount in the epoxy matrix the elongation and the straight at break decrease, while the flexural modulus increases [45][46][47]. In general, the same content [% wt] of ash and calcium carbonate affects the composite flexural behavior similarly. The flexural modulus and flexural strength of CaCO 3 /epoxy and stabilized sample/epoxy composites with different filler amount are shown in Figures 5 and 6, respectively.
Appl. Sci. 2020, 10, x FOR PEER REVIEW 9 of 15 CaCO3/epoxy and stabilized sample/epoxy composites with different filler amount are shown in Figures 5 and 6, respectively. Figure 5 shows the trend of flexural modulus of stabilized sample-epoxy and calcium carbonateepoxy composites at different filler content (from 10% up to 70% by weight). It should be noted that the flexural modulus of stabilized sample (ash) and calcium carbonate composites is similar for each filler content and the curves almost overlap. The flexural modulus remains approximately constant up to a filler amount of 30% wt, then it slightly increases to a filler amount of 50% and it strongly increases for filler amount of 70%wt. In general, the flexural modulus raises increasing the filler content by more than 30% by weight of filler content independently of whether the filler is stabilized sample or calcium carbonate.  Figure 6 shows the trend of flexural strength for of stabilized sample-epoxy and calcium carbonate-epoxy composites at different filler content (from 10% up to 70% by weight). Flexural strength and elongation at brake reduction of composites decreased with increasing of filler loading mainly due to agglomeration process acting as defects in the polymer matrix. It is worthwhile to note that the flexural strength decreases increasing the filler content up to 30% by weight for both ash and calcium carbonate. The composite stabilized sample-epoxy shows a constant decrease in the flexural strength up to a filler content of 50% wt and then it shows a slight increase up to 70% wt. Due to this trend and its standard deviation, it is possible to consider the flexural strength constant for stabilized sample content above 30% wt as well as for calcium carbonate composite. The experimental data show a change in tendency of flexural modulus and strength for stabilized FA and calcium carbonate content greater than 30% by weight.    Figure 6 shows the trend of flexural strength for of stabilized sample-epoxy and calcium carbonate-epoxy composites at different filler content (from 10% up to 70% by weight). Flexural strength and elongation at brake reduction of composites decreased with increasing of filler loading mainly due to agglomeration process acting as defects in the polymer matrix. It is worthwhile to note that the flexural strength decreases increasing the filler content up to 30% by weight for both ash and calcium carbonate. The composite stabilized sample-epoxy shows a constant decrease in the flexural strength up to a filler content of 50% wt and then it shows a slight increase up to 70% wt. Due to this trend and its standard deviation, it is possible to consider the flexural strength constant for stabilized sample content above 30% wt as well as for calcium carbonate composite. The experimental data show a change in tendency of flexural modulus and strength for stabilized FA and calcium carbonate content greater than 30% by weight. Figure 6. Flexural strength as a function of filler content. Figure 6. Flexural strength as a function of filler content. Figure 5 shows the trend of flexural modulus of stabilized sample-epoxy and calcium carbonate-epoxy composites at different filler content (from 10% up to 70% by weight). It should be noted that the flexural modulus of stabilized sample (ash) and calcium carbonate composites is similar for each filler content and the curves almost overlap. The flexural modulus remains approximately constant up to a filler amount of 30% wt, then it slightly increases to a filler amount of 50% and it strongly increases for filler amount of 70%wt. In general, the flexural modulus raises increasing the filler content by more than 30% by weight of filler content independently of whether the filler is stabilized sample or calcium carbonate. Figure 6 shows the trend of flexural strength for of stabilized sample-epoxy and calcium carbonate-epoxy composites at different filler content (from 10% up to 70% by weight). Flexural strength and elongation at brake reduction of composites decreased with increasing of filler loading mainly due to agglomeration process acting as defects in the polymer matrix. It is worthwhile to note that the flexural strength decreases increasing the filler content up to 30% by weight for both ash and calcium carbonate. The composite stabilized sample-epoxy shows a constant decrease in the flexural strength up to a filler content of 50% wt and then it shows a slight increase up to 70% wt. Due to this trend and its standard deviation, it is possible to consider the flexural strength constant for stabilized sample content above 30% wt as well as for calcium carbonate composite. The experimental data show a change in tendency of flexural modulus and strength for stabilized FA and calcium carbonate content greater than 30% by weight.

SEM-EDXS Analysis
SEM-EDXS was performed on the longitudinal surface of the specimens, that were in contact with the mold. Figure 7 presents SEM images of 50% wt stabilized sample filled epoxy composite in comparison with 50% wt CaCO 3 filled epoxy composite. SEM images demonstrate a significant difference between stabilized sample and CaCO 3 based composite. Indeed, the composite material with stabilized sample filler exhibits a non-homogeneous dispersion of particles with different dimensions, characterized by large agglomerates. These results are confirmed by the EDX maps (see Figure 8) that show the distribution of Ca in different % wt filler. On the other hand, a homogeneous distribution is associated with a better dispersion, with particles with diameter below 60 µm observed for composite with CaCO 3 . Ca was chosen because is present in both fillers and its quantity is limited in the epoxy-resin matrix. This allows us to highlight that particle agglomeration takes place in the case of the new fillers composite. Besides, particle cluster occur above 10% wt of stabilized sample, thus leading to a larger particle size and hence, strengthening decrease. When particles aggregation occurred, due to the interactions between them within the polymer matrix, the particle size increased and led to the creation of stress concentration points, which act as crack initiation and eventually weakened the interfacial adhesion between the matrix and particle [46]. The addition of stabilized sample fillers to the composite material leads to the poor distribution of particles in the resin matrix [47].

SEM-EDXS Analysis
SEM-EDXS was performed on the longitudinal surface of the specimens, that were in contact with the mold. Figure 7 presents SEM images of 50% wt stabilized sample filled epoxy composite in comparison with 50% wt CaCO3 filled epoxy composite. SEM images demonstrate a significant difference between stabilized sample and CaCO3 based composite. Indeed, the composite material with stabilized sample filler exhibits a non-homogeneous dispersion of particles with different dimensions, characterized by large agglomerates. These results are confirmed by the EDX maps (see Figure 8) that show the distribution of Ca in different % wt filler. On the other hand, a homogeneous distribution is associated with a better dispersion, with particles with diameter below 60 µm observed for composite with CaCO3. Ca was chosen because is present in both fillers and its quantity is limited in the epoxyresin matrix. This allows us to highlight that particle agglomeration takes place in the case of the new fillers composite. Besides, particle cluster occur above 10% wt of stabilized sample, thus leading to a larger particle size and hence, strengthening decrease. When particles aggregation occurred, due to the interactions between them within the polymer matrix, the particle size increased and led to the creation of stress concentration points, which act as crack initiation and eventually weakened the interfacial adhesion between the matrix and particle [46]. The addition of stabilized sample fillers to the composite material leads to the poor distribution of particles in the resin matrix [47].  From the elemental characterization provided by different chemical EDXS analyses (Table 3), the increase of filler amount causes a decrease in the C and Cl content, while increases Ca amount. In case of composite with stabilized sample, Al, Mg, K and S presence has been noticed, due to the initial chemical composition of the FA. It is important to highlight the limit of the instrument with light

SEM-EDXS Analysis
SEM-EDXS was performed on the longitudinal surface of the specimens, that were in contact with the mold. Figure 7 presents SEM images of 50% wt stabilized sample filled epoxy composite in comparison with 50% wt CaCO3 filled epoxy composite. SEM images demonstrate a significant difference between stabilized sample and CaCO3 based composite. Indeed, the composite material with stabilized sample filler exhibits a non-homogeneous dispersion of particles with different dimensions, characterized by large agglomerates. These results are confirmed by the EDX maps (see Figure 8) that show the distribution of Ca in different % wt filler. On the other hand, a homogeneous distribution is associated with a better dispersion, with particles with diameter below 60 µm observed for composite with CaCO3. Ca was chosen because is present in both fillers and its quantity is limited in the epoxyresin matrix. This allows us to highlight that particle agglomeration takes place in the case of the new fillers composite. Besides, particle cluster occur above 10% wt of stabilized sample, thus leading to a larger particle size and hence, strengthening decrease. When particles aggregation occurred, due to the interactions between them within the polymer matrix, the particle size increased and led to the creation of stress concentration points, which act as crack initiation and eventually weakened the interfacial adhesion between the matrix and particle [46]. The addition of stabilized sample fillers to the composite material leads to the poor distribution of particles in the resin matrix [47].  From the elemental characterization provided by different chemical EDXS analyses (Table 3), the increase of filler amount causes a decrease in the C and Cl content, while increases Ca amount. In case of composite with stabilized sample, Al, Mg, K and S presence has been noticed, due to the initial chemical composition of the FA. It is important to highlight the limit of the instrument with light From the elemental characterization provided by different chemical EDXS analyses (Table 3), the increase of filler amount causes a decrease in the C and Cl content, while increases Ca amount. In case of composite with stabilized sample, Al, Mg, K and S presence has been noticed, due to the initial chemical composition of the FA. It is important to highlight the limit of the instrument with light elements such as C; however, although the C amount is expressed in a semi-quantitative way, it becomes very useful for the comparative analysis between the two examined compounds.

Sustainability Evaluation of the Proposed Technology
EE and CF parameters of the synthesis of the proposed new filler were considered to evaluate environmental sustainability.
Data about EE and CF of the recycled stabilized material were obtained by using the CES Selector software [48] taking into account the stabilization procedure, which involves the bottom ash grinding and considering the mixing of different ashes typologies, as described in the experimental section and discussed in literature [21]. For the stabilized material, an embodied energy ranging from 0.061 to 0.062 MJ/kg and a CO 2 footprint of about 0.03 kg/kg resulted. Table 4 reports the SUB-RAW indices evaluated by comparing the new proposed material with respect to calcite, which is a natural resource that is often used as a filler, to produce some composites. As a reference, this index was also calculated in comparison with sandstone, talc and resin used to synthesize the composites for this work. From calculated SUB-RAW indices, it is evident that the new proposed inert is more sustainable if compared to some natural resources, as for example calcite, talc and sandstone. Obviously it is also more sustainable with respect to a resin [49]. Then, it is possible to conclude that it may be used to produce composited materials. In principle, its market applicability is potentially very promising. To evaluate this, also the price of the materials reported in this work have been considered. Figure 9 shows the EE for several materials (ceramic, glass and composites) as a function of their commercial price. Data were obtained from CES Selector 2019 [48]. Data on the carbon footprint of the same materials, reported as a function of their commercial price, have the same behavior already shown by Bontempi et al. [34], therefore they are not reported in this paper. In correspondence of the EE of the new proposed material, an orange dotted horizontal line is reported. From the analysis of Figure 9, it can be seen that the new obtained stabilized material can be compared to wollastonite in terms of the EE environmental parameter used to quantify the sustainability of a material. Figure 9 shows that the energy needed to synthesize the new proposed material is lower than that of the almost majority of ceramic and glass materials. It results evident that it is more sustainable that the previous proposed COSMOS filler, obtained by adding an external silica source [16,39] to stabilize MSWI FA. Indeed, EE of COSMOS resulted higher than that of calcite. On the contrary, in the present case, it is demonstrated that the new obtained stabilized material can be used, with environmental advantages, in substitution of calcite. This is due to the fact that BA is a by-product produced on the same incinerator plant where FA is generated. As a consequence, its EE and CF can be assumed to be zero. It is possible to conclude that the new filler is strongly suggested to be used for the synthesis of composites materials, avoiding the natural resources employ. The price, which is generally used to evaluate the commercial applications of a material, is an important criterion, which must be also taken into account, because it can be related to the new material market. In the present case, this is unknown but the Figure 9 reports the price of several materials, allowing us to verify the market opportunities for the new proposed filler.

Conclusions
Recently, a new stabilization technology developed to treat MSW incineration FA has been proposed. It is based on the use of bottom ash, produced at the same incinerator plant. This new process is considered a zero-waste approach, because it involves the use of waste materials produced on the same plant. As a consequence, the landfilling of these wastes can be neglected, following the recommended material use close loop by utilizing 'waste' for suitable and sustainable applications.
This work demonstrates the sustainability of the proposed technology by using a new simplified approach and allowing to compare the obtained inert material with natural resources.
In addition, the effects of the new produced filler on the structure and properties of obtained composites based on the use of a resin are assessed by means of structural and mechanical analyses. For comparison purposes, also calcite (CaCO3) was used as a standard filler, to formulate composites that were produced and analyzed under the same conditions.
Regarding mechanical properties of the new stabilized sample-composite, the comparison with CaCO3 based formulation shows comparable values in terms of flexural modulus and flexural strength that raise by increasing the filler content around 30% wt, independently of filler type, stabilized sample or calcium carbonate, respectively. The amount of CaCO3 or stabilized sample in From the analysis of Figure 9, it can be seen that the new obtained stabilized material can be compared to wollastonite in terms of the EE environmental parameter used to quantify the sustainability of a material. Figure 9 shows that the energy needed to synthesize the new proposed material is lower than that of the almost majority of ceramic and glass materials. It results evident that it is more sustainable that the previous proposed COSMOS filler, obtained by adding an external silica source [16,39] to stabilize MSWI FA. Indeed, EE of COSMOS resulted higher than that of calcite. On the contrary, in the present case, it is demonstrated that the new obtained stabilized material can be used, with environmental advantages, in substitution of calcite. This is due to the fact that BA is a by-product produced on the same incinerator plant where FA is generated. As a consequence, its EE and CF can be assumed to be zero. It is possible to conclude that the new filler is strongly suggested to be used for the synthesis of composites materials, avoiding the natural resources employ. The price, which is generally used to evaluate the commercial applications of a material, is an important criterion, which must be also taken into account, because it can be related to the new material market. In the present case, this is unknown but the Figure 9 reports the price of several materials, allowing us to verify the market opportunities for the new proposed filler.

Conclusions
Recently, a new stabilization technology developed to treat MSW incineration FA has been proposed. It is based on the use of bottom ash, produced at the same incinerator plant. This new process is considered a zero-waste approach, because it involves the use of waste materials produced on the same plant. As a consequence, the landfilling of these wastes can be neglected, following the recommended material use close loop by utilizing 'waste' for suitable and sustainable applications.
This work demonstrates the sustainability of the proposed technology by using a new simplified approach and allowing to compare the obtained inert material with natural resources.
In addition, the effects of the new produced filler on the structure and properties of obtained composites based on the use of a resin are assessed by means of structural and mechanical analyses.
For comparison purposes, also calcite (CaCO 3 ) was used as a standard filler, to formulate composites that were produced and analyzed under the same conditions.
Regarding mechanical properties of the new stabilized sample-composite, the comparison with CaCO 3 based formulation shows comparable values in terms of flexural modulus and flexural strength that raise by increasing the filler content around 30% wt, independently of filler type, stabilized sample or calcium carbonate, respectively. The amount of CaCO 3 or stabilized sample in the composites is the main factor causing a reduction in the mechanical properties mainly due to the crowding effect. EDX maps highlighted a more homogeneous distribution of Ca in CaCO 3 -composites with respect to stabilized sample-composites, due to the lower particle dimension in calcite powder.
In summary, it is possible to conclude that the new proposed filler, realized by using stabilized MSWI fly ash, can be used to produce sustainable composites, allowing to preserve natural resources, as for example of calcite, demonstrating similar mechanical and structural performance and with great environmental and economic benefits.
If Europe-wide implementation of waste recovery is to be part of the circular economy strategy, it is expected that one of the political priorities should be the implementation of a legal framework that can support new technologies and materials availability for the recycling sectors.