1. Introduction
Accelerated plastic use over the years has created an enormous quantity of waste plastic. In 2021, 390.7 million metric tons of waste plastic was produced globally [
1]. Despite the continued increase in plastic production, only 9% of this volume is recycled [
2]. For the plastic that does not get recycled, 22% is mismanaged, 19% is incinerated, and the remaining 50% is directed to landfill [
2]. This suboptimal waste plastic disposal has widespread negative environmental effects [
3]. The vast amount of unrecycled plastic presents a substantial opportunity to profitably utilize available materials, reduce pollution, and redirect waste from landfills.
One such application of waste plastic that continues to be investigated is the use of polymers as a replacement aggregate or fiber reinforcement in concrete [
4]. Traditional concrete is the most used material globally, with approximately 30 billion metric tons of concrete being consumed each year [
5]. The manufacturing of concrete, however, also makes it one of the most detrimental materials for the environment [
6]. A typical concrete mixture consists of 12% Portland cement, 34% sand, 28% crushed stone, and 6% water by weight [
6]. Of this mixture, Portland cement alone makes concrete the contributor of 8% of all global carbon emissions [
7,
8]. If concrete were compared against global contributors of greenhouse gases as a country, it would be the third largest producer – only surpassed by the United States and China [
8,
9,
10]. These large carbon emissions are almost exclusively a result of the manufacturing process of Portland cement [
6]. Between the fossil fuel combustion to operate the rotary kiln, and the high temperatures required for the calcination of limestone, every 1 ton of cement contributes to 1.25 tons of carbon dioxide (CO
2) production [
6]. Globally, the emissions from cement production continue to grow annually reaching a new peak of 1.7 billion metric tons of CO
2 in 2021 [
11]. To reduce the total emissions from concrete, many studies have been conducted in search of a less energy intensive binder to replace Portland Cement [
12]. These existing studies have investigated the use of industrial waste products as supplementary cement materials (SCM) and have already demonstrated some select successful replacements for Portland cement. These substitutes include, but are not limited to, palm oil fuel ash (POFA) [
13], rice husk ash (RHA) [
13], palm oil clinker powder (POCP) [
14], ground granulated blast-furnace slag (GGBS) [
15], pulverized fly ash (PFA) [
16], corn cob ash [
17]. While many of these materials have demonstrated merit, they are often associated with a lack of supply and localization of use. GGBS and PFA are both industrial waste products and are only produced in quantities that match only 5-10% of cement production [
18]. Another research study has shown that up to 70% of the concrete mix can be replaced by treated POFA while retaining average mechanical properties [
14]. The use of up to 30% recycled concrete aggregate in the mixture has also shown a 29% decrease in CO
2 emissions [
13]. Despite these aggressive carbon contributions and a production rate by weight that eclipses all other materials including plastics, concrete is often not immediately associated with unsustainable environmental practices. The problem of concrete, however, is more severe than plastic, with the total weight of plastic produced in 60 years being matched by concrete in only two [
10]. Beyond carbon emissions, concrete is also responsible for demanding 18% of global industrial water consumption and 9% of global industrial water withdrawal annually [
19]. A direct correlation can be observed between regions that experience greater water stress, and higher production of concrete in the United States, the Middle East, India, and China [
19]. On all accounts, concrete works to remove natural spaces, decrease ecological diversity, and increase water demands on already stressed environments all while aggressively contributing to global emissions.
Extrapolating beyond waste plastic aggregates, plastic applications have seen use as full material substitutes in the experimental testing of plastic sand bricks [
20]. Traditional bricks rely on cement as a key material in their manufacture and therefore also contribute to growing annual carbon emissions. By utilizing sand as the bulk aggregate and a liquid thermoplastic as the binder, plastic sand bricks have demonstrated potential as a new building material [
20]. Together, these solutions work to offset the cost and emissions associated with the manufacture and use of virgin construction materials while also providing a new opportunity for recycling [
4]. Using plastic composites to replace existing building materials can pave the way toward a more circular economy and reduced environmental impact [
20].
The current research field surrounding plastic composites for use as building materials consists of combining cement with fine aggregate plastics, lightweighting approaches for traditional concrete based on aggregate density, plastic additives in unfired clay brick, and soil-cement blocks [
20]. Existing plastic sand brick studies have developed methods for producing to-scale bricks and subjecting them to compressive strength, tensile strength, efflorescence, thermal resistance, and water absorption tests [
21,
22]. The typical thermoplastics used across these studies were limited to polyethylene (PE), low density polyethylene (LDPE), high density polyethylene (HDPE), polyvinylchloride (PVC), polypropylene (PP), and polystyrene (PS) [
23]. On average, these studies found that plastic sand bricks demonstrated an initial decline in compressive strength at low percentages of sand but experienced a peak in strength at 40% compositions and similar strength at 50% [
21]. The highest strength was recorded at 32.7 MPa for a 3:1 LDPE-sand material composition [
24]. This places plastic sand bricks at a comparable compressive strength to residential concrete which has a strength range from 23.3 MPa to 30.2 MPa in commercial structures [
25]. High strength concrete, however, is more difficult to replicate as it can have compressive strength ratings exceeding 70–80 MPa [
26].
The existing research has demonstrated potential for using recycled plastic as a substitute for traditionally used building materials in construction. This study extends this research by investigating the use of polycarbonate (PC) in plastic sand bricks as a new material. The characteristics of PC make it a desirable material for applications demanding high compressive strength, durability, impact strength, thermal resistivity, clarity, fatigue resistance, and UV resistance [
27]. It is readily used in commercial applications such as storefront windows, protective barriers and safety glass, vehicle components, electronic housings, and medical diagnostic equipment [
27,
28]. The highest demand for PC are in the automotive industry due to its high performance strength properties in conjunction with its light weight [
28]. In 2020, the global capacity for PC was 6.1 million tons annually with a projected continued growth of 8% in upcoming years [
29]. This high production rate and potential source of waste plastic, coupled with the high compressive strength properties of PC (76 – 86.2 MPa for molded PC) as an engineering plastic makes it a desirable substitute for typically high strength concrete applications [
30]. This work provides a repeatable test method and mold to produce a matrix of sand-plastic sample compositions with dimensions adhering to ASTM D695 standard test method for compressive properties of rigid-plastics [
31]. The testing consisted of compositions of 0% (control), 20%, 30%, 40%, and 50% sand by weight based on proven success ranges of sand-plastic ratios across previous studies with different plastics [
24]. Each sample was subjected to compressive strength tests until yield and their resulting stress-strain behavior were plotted. The results are presented and discussed in the context of plastic recycling and the circular economy.
3. Results
The plastic sand bricks produced demonstrated macrohomogeneity and minimal porosity. At low sand compositions (30% sand and below), the samples’ viscosity and appearance were nearly identical to pure PC. The increase from 30% to 40% sand, however, showed a dramatic increase in both visible sand and working texture. While liquid, high sand compositions (40% and 50% sand) were more viscous than the low sand compositions and the cooled bricks retained a “gritty” texture. This resulting gradient is demonstrated in
Figure 7 where the stark contrast between 20% sand and 50% sand can be seen.
After each sample was subjected to a compression test to failure, the resulting stress-strain curves were plotted and compared against a 100% recycled PC sample produced using the same mold and process. The resulting strength behavior in
Figure 8 was observed.
Figure 8 shows that the addition of sand directly affects the compressive strength, compressive modulus, and failure mode of a PC sand brick. At low sand compositions, the compressive yield strength has notably lower averages than the 71 MPA recorded for 100% PC with a minimum of 51 MPa at 20% sand. As the percentage of sand increases, the compressive strength of the samples also increases until a maximum of 71 MPa at 50% sand is reached. The reduced strength at low sand compositions can be associated with an additive threshold for which sand behaves as an impurity at insufficient amounts and as a reinforcement above this threshold. The compressive modulus or compressive stiffness (slope of the linear region prior to plastic yield) of the low sand compositions has no change from the control at an average of 1.43 GPa, but increases with higher sand contributions to ultimately exceed the control at 50% sand and achieve a modulus of 2.44 GPa. The maximum and average compressive strengths of each PC sand composition are summarized in
Figure 9.
The 40% and 50% sand compositions experienced more consistent response to stress between trials, and their strength was comparable to the 100% PC control than samples with lower percentage contributions of sand. This is shown by the higher standard deviations for 20%, and 30% sand in comparison to the lower deviations for 40% and 50% sand samples (
Figure 10).
At 50% sand composition, the critical distinction from 100% recycled PC is the increase to compressive modulus and the change in failure mechanism. As the ratio of sand increases, the compressive stiffness of the brick increases, and the plastic region of the curve following yield plateaus (
Figure 8). This pattern deviates from the low sand compositions in which the higher ratio of PC allows the sample to continue to deform and flow at increasingly high stresses and strains. This can be seen by comparing the control values at fracture to the sand samples in
Figure 8. The 100% PC control has a smooth plastic region that increases exponentially until fracture at a final strain of 0.63. Alternatively, the 50% sand samples achieve a strain of only 0.49 after a plateau equivalent to the yield strength. A gradient of incrementally lower fracture stress and strains can be observed as the percentage of sand increases from 20% to 50% until a minimum is reached at 50%. This pattern is a product of the thermoplastics ability to flow and the tradeoff to the more brittle shear/cracking behavior of a concrete-like material as sand is added [
36]. The high strains at fracture associated with lower sand compositions can only be achieved by having material flow outward to conserve the sample material and increase the effective cross section capable of withstanding higher stresses. This change in cross section and flow behavior is emphasized in
Figure 10. While this high stress at fracture would suggest increased structural potential, the severe strain and cross-sectional deformation makes this plastic region largely inconsequential to most load bearing cases. Alternatively, as the composition of sand is increased, the sample flows less, resulting in a lower strain, and less deformed neutral cross section.
The failure mechanism of high sand compositions more closely reflects that observed in concrete due to the transition from ductile to shear failure. This can be seen in
Figure 11 following the indicated shearing line of action. The PC acts as a binder for the sand and enables the sand to contribute to the rigidity of the sample. This explains the increase to strength and stiffness up to failure, at which point the sand begins to separate from the PC causing cracks to propagate between grains of sand and along the shear plane until the material crumbles to the same effect as concrete [
36]. The contribution of sand to crack propagation and shear failure can be observed by comparing the curves in
Figure 8. The control demonstrates a smooth stress vs. strain behavior in the plastic region following yield as the material flows. Alternatively, all sand composites show visible fluctuations from a theoretical smooth curve in the plastic region with more appearing as the percentage of sand is increased. The moment sand is introduced to the material, the smooth flow behavior of the thermoplastic is interrupted to a varying degree dependent on the amount of sand used.
Therefore, it can be concluded that 50% sand composition most closely mimics high performance concrete at a reduced density of 1.86 g/cm3 and contributes to an increased compressive stiffness, increased compressive strength, and shear failure at lower strains than 100% recycled PC.
Author Contributions
Conceptualization, J.M.P.; methodology, M.W., A.K., and J.M.P.; validation, M.W., A.K., and J.M.P.; formal analysis, M.W. and A.K.; investigation, M.W. and A.K.; resources, J.M.P.; data curation, M.W., A.K., and J.M.P.; writing—original draft preparation, M.W., A.K., and J.M.P.; writing—review and editing, M.W., A.K., and J.M.P; visualization, M.W.; supervision, J.M.P.; project administration, J.M.P.; funding acquisition, J.M.P. All authors have read and agreed to the published version of the manuscript.