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Yu, W., Han, X., Cai, H., Lu, W., Xu, H., and Yi, W. (2021). "Feasible management of non-degradable agricultural mulching film wastes into functional flame-retarded materials," BioResources 16(2), 2838-2852.

Abstract

A feasible procedure was proposed to convert agriculture mulching film wastes into functional flame-retarded cotton stalk particles-polyethylene-sandy soil composites (CS-PE-SSx) by simple compounding and injection molding. Due to the uniform dispersion of solid particles in polymer matrix and the promising interfacial combination and the potential interacting forces between cotton stalk and sandy soil particles, the resultant composites showed promising mechanical strength (a flexural strength of approximately 29.0 MPa, a tensile strength of approximately 15.8 MPa, and an impact strength of approximately 3.17 kJ/m2) and improved thermal stabilities. The addition of sandy soil particles endowed materials with favorable flame-retarded properties, which can be resistant to fire ignition and flame out within 55 s. Moreover, the actual agriculture wastes containing mulching film residues, cotton stalk, and soil from different areas of China were also successfully transformed into functional composites, which exhibited promising mechanical, thermal, and flame-retarding properties. This study provided a simple, green, and low-cost strategy to convert agriculture mulching film wastes into functional materials, which can be recommended as a viable option to solve the problem of agriculture mulching film wastes.


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Feasible Management of Non-degradable Agricultural Mulching Film Wastes into Functional Flame-retarded Materials

Wenfan Yu,a,b Xiangsheng Han,a,b Hongzhen Cai,a,b Wenyu Lu,a,b Hang Xu,a,b and Weiming Yi a,b,*

A feasible procedure was proposed to convert agriculture mulching film wastes into functional flame-retarded cotton stalk particles-polyethylene-sandy soil composites (CS-PE-SSx) by simple compounding and injection molding. Due to the uniform dispersion of solid particles in polymer matrix and the promising interfacial combination and the potential interacting forces between cotton stalk and sandy soil particles, the resultant composites showed promising mechanical strength (a flexural strength of approximately 29.0 MPa, a tensile strength of approximately 15.8 MPa, and an impact strength of approximately 3.17 kJ/m2) and improved thermal stabilities. The addition of sandy soil particles endowed materials with favorable flame-retarded properties, which can be resistant to fire ignition and flame out within 55 s. Moreover, the actual agriculture wastes containing mulching film residues, cotton stalk, and soil from different areas of China were also successfully transformed into functional composites, which exhibited promising mechanical, thermal, and flame-retarding properties. This study provided a simple, green, and low-cost strategy to convert agriculture mulching film wastes into functional materials, which can be recommended as a viable option to solve the problem of agriculture mulching film wastes.

Keywords: Agriculture waste; Sandy soil; Recyclability; Flame retardant; Materials

Contact information: a: School of Agricultural Engineering and Food Science, Shandong University of Technology, Zibo, 255000, China; b: Shandong Research Center of Engineering and Technology for Clean Energy, Zibo, 255000, China; *Corresponding author: yiweiming@sdut.edu.cn

GRAPHICAL ABSTRACT

INTRODUCTION

Plastic mulching film, one of the most commonly used materials in agricultural production, can conserve soil moisture and increase soil temperature in areas where irrigation is not available and the spring temperature is low; other benefits include higher crop yield and better crop quality (Gu et al. 2017; Lee et al. 2019; Chen et al. 2020; Hu et al. 2020). Typically, the major component of mulching film is low density and linear low-density polyethylene (Briassoulis and Schettini 2003; Kasirajan and Ngouajio 2012). This material is difficult to biodegrade due to its unique molecular structure and crystallinity, resulting in a great environmental burden (Ng et al. 2018). Because of the incomplete recovery after the crop season, waste mulching film debris accumulates in soil, which negatively affects the soil quality, entangles with crop roots, and inhibits the absorption of water and nutrients, thus decreasing the crop yields and limiting the sustainable development of agriculture (Liu et al. 2018; Qi et al. 2018; de Souza Machado et al. 2019). Moreover, such plastic residues remaining in agricultural soil can enter the ecosystem, and the microplastics may be migrated by soil organisms as carriers for other soil pollutants, or become dust in the air, threatening the environment (Steinmetz et al. 2016; He et al. 2018). Thus, how to deal with mulching film waste in effective, green, and low-cost ways is an urgent problem needed to be solved in both agricultural production and environmental protection.

Many attempts have been made to deal with the agricultural mulching film wastes, such as the development and utilization of photodegradable or biodegradable materials, repeated use of plastics, weight reduction of mulching film, recycling, and incineration (Liu et al. 2014). Cyclic utilization and weight reduction of mulching film seems to be the simple way to deal with waste plastic residues. However, this strategy can only temporarily alleviate the aggravation of the problem, and collecting plastic in farmland will take a lot of time and labor. Incineration is the direct burning of agricultural residues in the field, which is another simple and direct method of waste treatment. Unfortunately, this option inevitably releases some air-borne particulates, greenhouse gas, and poses other serious consequences for the environment (Nkwachukwu et al. 2013; Vox et al. 2016). Biodegradable materials, such as mulching film, can be decomposed into small molecules after harvest season, becoming a promising strategy to reduce the pollution of the soil by plastic fragments. However, when biodegradable plastics are used in the actual environment, they often face the restriction of many environmental factors (e.g., temperature, pH, or moisture) and enzymatic factors (e.g., enzyme preference for plastic polymer), making the degradation of biodegradable plastics complicated and unpredictable (Lambert and Wagner 2017; Sanchez-Hernandez et al. 2020). Mulching film can also be turned into fuel for power plants. Although this option can protect the environment and save energy, the large amount of pollutants carried on the mulching film and the cost pressure brought by the recovery make it difficult to effectively implement the mulching film collection (Hemphill 1993).

Recently, wood-plastic composites are emerging as favorable options to recycle agriculture wastes. The concept of wood-plastic composites is straightforward: fine powder of wood, or woody biomass from agricultural residues, is blended with polymers, such as polyethylene or polypropylene, via extrusion, injection, or compression moulding to form simple sections, such as planks, or more complex profiles (Chan et al. 2017; Mohanty et al. 2018). Wood-plastic composites have many advanced properties, such as low moisture absorption, low density, resistance to biological attack, good dimensional stability, and a combination of high specific stiffness and strength (Sommerhuber et al. 2015). As a consequence, they are widely used by owners in different fields, such as different outdoor and indoor applications, like fencing, decking, railing, docks, landscaping timbers, windows, doors, and various parts of automobiles (Borah and Kim 2016). For the improvement of the material properties of wood-plastic composites, inorganic fillers, including red mud (Liu et al. 2016), mineral fillers (Guzel et al. 2016), montmorillonite (Zhu et al. 2019), nano-zinc oxide (Abdel-Rahman et al. 2020), and nano-silica (Hao et al. 2018; Ma et al. 2019), are added into the materials. For example, Vigneshwaran et al. (2019) used red mud and sisal fiber as fillers to reinforce unsaturated polyester resin, and the addition of red mud improved mechanical and waterproof properties of composites. Matykiewicz et al. (2019) added basalt powder to epoxy resin to enhance the thermomechanical properties, stiffness, and hardness of the composites. Liu et al. (2016) modified wood flour (WF) with sodium-montmorillonite (Na-MMT) and then compounded with polylactic acid (PLA). The physical properties, most of the mechanical properties, and thermal properties of the obtained composites were improved. Sandy soil is also an inorganic matter, and after crops were harvested, it will inevitably adhere to the mulching film wastes and agricultural residues. Thus, an opportunity was provided to convert mulching film wastes and inorganic soil into functional wood-plastic composites with favorable strength and potential flame retarded properties, which were suitable as building materials, interior decoration, landscaping wood, doors and tables, etc.

Herein, cotton stalk particles-polyethylene-sandy soil composites (CS-PE-SSx) were fabricated by simple high-speed mixing, mini-twin-screw extrusion, and micro injection molding procedures. Unlike traditional preparation of wood-plastic composites that use maleic acid polyethylene (MAPE) as compatibilizer to optimize the interface combination between hydrophobic polyethylene matrix and hydrophilic biomass (Tong et al. 2014; Mu et al. 2018), the addition of sandy soil (without MAPE) offered a procedure with easy preparation capability and relatively low cost. Due to the uniform dispersion of solid particles in the polymer matrix, the promising interface combination and the potential interacting forces between biomass and the oxygen groups on the surface of sandy soil, the resultant composites exhibited improved mechanical strength (flexural strength of approximately 29.0 MPa, tensile strength of approximately 15.8 MPa, and an impact strength of approximately 3.17 kJ/m2). Due to the intrinsic flame-retarded properties of inorganic sandy soil and their uniform distribution in polymer matrix, the composites also showed a higher limiting oxygen index (LOI) value of 24.1% compared with 20.8% of composites without sandy soil. The composites were barely ignited by flame envelope for 10 s and exhibited flame out within 55 s. Furthermore, composites were also obtained by actual agriculture mulching film wastes from different areas of China (e.g., Shandong, Jiangsu, and Xinjiang). This work may pave a simple, green, and low-cost way for the feasible management of mulching film wastes into functional flame-retarded materials.

EXPERIMENTAL

Materials

High-density polyethylene (HDPE, 9001) with a melt flow index of 0.05 g/10 min was purchased from Taiwan Plastic Co., Ltd. (Taiwan, China). Linear low-density polyethylene (LLDPE, PF0218) with a melt flow index of 2 g/10 min was bought from Xingyu Plastic Chemical Co., Ltd. (Suzhou, China). The cotton stalk (CS) was from Liaocheng, China, and crushed as particles with sizes between 80- (178 µm) and 100-mesh (125 µm). The sandy soil (SS) with a particle size less than 140-mesh (104 µm) was obtained from Liaocheng, China.

Preparation of CS-PE-SSx Composites

The preparation procedure of CS-PE-SSx composites is illustrated in Fig. 1. Cotton stalk powder, sandy soil, and polyethylene (the main constituent in mulching film) were chosen as main components to imitate the natural agriculture wastes (Fig. 1A). As a bio-fiber, cotton stalk mainly consists of cellulose, hemicellulose, and lignin, and the fibrous morphology and the presence of polar groups (-OH, -COOH, and other polar groups) made them promising in the fabrication of functional composites (Zheng et al. 2015; Yang et al. 2019). Moreover, sandy soil mainly consists of silicon dioxide, which was characterized of the oxygen-containing group (-OH and -O-), may exist some interacting forces with bio-fiber and facilitate the materials manufacture (Wang et al. 2020).

Typically, sandy soil and cotton stalk were dried at 100 °C for 24 h. Then, specific ratios (Table 1) of dried cotton stalk powder, sandy soil, HDPE, and LLDPE were mixed in the dual-motion 3D high-speed mixer (JHN-15; Zhengzhou Jintai Metal Material Co., Ltd., Zhengzhou, China) at a speed of 15 r/min for 10 min (Fig. 1B). The mixtures were processed with the mini-twin-screw extruder (WLG10G, Shanghai Xinshuo Precision Machinery Co., Ltd., Shanghai, China) at a temperature of 180 °C and an extrusion speed of 60 r/min (Fig. 1C). Afterwards, the molten mixture was extruded into the barrel and then put into the micro injection molding machine (WZS10D, Shanghai Xinshuo Precision Machinery Co., Ltd., Shanghai, China) for injection molding (Fig. 1D). The barrel temperature was set at 180 °C, the material tube temperature was 45 °C, and the holding time was 5 s. The obtained composites were abbreviated as CS-PE-SSx, where x represented the contents of SS in composites.

Fig. 1. Schematic synthesis of CS-PE-SSx composites: (A) photographs of cotton stalk, mulching film, and sandy soil (the brown frame emphasizes the main components of cotton stalks, polyethylene, and sandy soil); (B) High-speed mixing; (C) Mini-twin-screw extruding; (D) Micro injection molding and the photograph of CS-PE-SSx composite samples

Characterization

Fourier transform infrared (FT-IR) analysis was performed on a Nicolet 5700 FT-IR spectrometer (Thermo Fisher Scientific, Waltham, MA, USA) using the KBr pellet method at wavenumber range 400 to 4000 cm-1. The samples were crushed into powders and washed with ethanol three times and dried at 60 °C for 24 h. The specimens for FT-IR measurement were prepared by grinding the sample solid with KBr together and then compressed into thin pellets.

X-ray diffraction (XRD) analysis was performed on a Bruker AXS D8 advance polycrystalline X-ray diffractometer (BRUKER AXS GMBH, Karlsruhe, Germany) using CuKα radiation. The operating voltage was 40 KV, the operating current was 50 mA, the sweep range was 5° to 60°, and the scanning speed was 5°/min. The samples were crushed, washed with ethanol three times, and dried at 60 °C for 24 h before XRD study.

Field emission scanning electron microscopy (FE-SEM, FEI Sirion 200; Thermo Fisher Scientific, Waltham, MA, USA) was used to characterize the surface microstructure of samples. The scanning voltage was set as 10 kV. Energy-dispersive X-ray spectroscopy mapping of broken samples was performed to verify the presence and distribution of SS in CS-PE-SSx composites.

The thermal stabilities of the samples were evaluated using a synchronous thermal analyzer (STA 449, NETZSCH Scientific Instruments Trading Ltd., Selb, Germany). The experiments were conducted in nitrogen atmosphere (20 mL/min) with the heating process from 30 °C to 1100 °C under a 10 °C/min heating rate.

Mechanical properties

The tensile and flexural properties of the samples were tested with an electronic universal testing machine (WDW1020; Changchun Kexin Co., Ltd., Changchun, China). The samples were cut into dimensions of 80 × 10 × 4 mm3 for flexural properties testing, with a 64 mm bending span and a 5 mm/min loading speed. Samples with dimensions of 150 × 10 × 4 mm3 were used for tensile properties tests with a 10 mm/min stretching speed. The impact performance of the samples (80 × 10 × 4 mm3) was tested using a pendulum electronic impact tester (JB-300b; Jinan Hengsi Shengda Instrument Co., Ltd., Jinan, China) under an impact energy of 1 J. All the mechanical properties tests were processed for more than five replicates and averaged for each test.

Flame-retarded properties

The flame-retardant properties of samples were studied by evaluating their combustion processes. Typically, on one hand, the CS-PE-SSx samples (20 × 10 × 4 mm3) with different SS contents were ignited by flame envelope for 10 s, and their burning status and flame sizes were recorded. On the other hand, the CS-PE-SSx samples (25 × 10 × 4 mm3) with different SS contents were ignited and kept burning in the air, and their flame out time and burning extents were recorded. An intelligent oxygen index analyzer (ZR-01; Qingdao Shan Fang Instrument Co., Ltd., Qingdao, China) was used to measure the LOI values of CS-PE-SSx composites. The dimensions of samples were 80 × 10 × 4 mm3 and the mixed gas flow rate was 40 ± 2 mm/s. The LOI values and corresponding estimated standard deviation were calculated according to Eq. 1,

(1)

where OI represents the limiting oxygen index (vol%), Cf is the last oxygen concentration value (vol%) of each group of measurements, d represents the difference of the oxygen concentration of each measurement (vol%), and k is obtained by comparing the last six measurements to find the standard. The value of d can be optimized according to Eqs. 2 and 3,

(2)

(3)

where σ represents the standard deviation, ci is the oxygen concentration (vol%) obtained from the last six measurements of each group, and n is the number of measurements of the oxygen concentration. If d < (2σ) / 3, then increase the value of d and repeat the experiment until the condition is met. If d > 1.5σ, then decrease the value of d and repeat the experiment.

RESULTS AND DISCUSSION

FT-IR

The FT-IR analysis was carried out on SS, LLDPE, CS, and CS-PE-SSx with different SS contents (Fig. 2). For cotton stalk, the bands at 3419 cm−1, 2918 cm−1 and 2850 cm−1, 1743 cm−1, 1633 cm−1, 1510 cm−1 and 1455 cm−1, 1426 cm−1 and 1375 cm−1, were attributed to the hydrogen bonded O-H stretching vibration, C-H stretching vibration from -CH and -CH2 in cellulose and hemicellulose components, C=O valance vibration of hemicellulose acetyl group or ester linkage of carboxylic group of feruli and p-coumeric acid in lignin, the vibration of C=O stretch of conjugated p-substituted aryl ketones, the -C=C- stretch of the aromatic rings of lignin, and -CH, -CH2 vibrations and aromatic ring modes, respectively (Fig. 2A) (Rahbar Shamskar et al. 2016). However, the characteristic peak at 1743 cm-1 and 1633 cm-1 exhibited blue shifts to 1735 cm-1 and 1624 cm-1 of CS-PE-SS40, indicating the changes of their chemical environment, which was triggered by the possible interactions between components in CS-PE-SS40 (Fig. 2B). The main component of sandy soil was silicon dioxide. The polar groups on the surface of silicon dioxide may contribute some interacting forces with biomass, resulting in the shift of the characteristic peaks in the FT-IR spectrum (Boehm 1966). Thus, the interaction between CS and SS indicated promising combination among components, mechanical properties, and functionalities.

Fig. 2. (A) The FT-IR spectra of CS, SS, LLDPE, and CS-PE-SSx composites with different SS contents; (B) The amplified FT-IR spectra at wavenumber 1600 to 1800 cm-1, emphasizing the blue shift of wavenumber

XRD

The XRD patterns of CS, HDPE, SS, and CS-PE-SS40 are shown in Fig. 3. The CS showed two regions with peak values of approximately 16.9° and 22.1°, demonstrated an amorphous state and cellulose I, respectively (Zhou et al. 2020). Two main diffraction peaks of the HDPE could be observed at 21.6° and 24°, which corresponded to (110) and (200) crystal planes (Zhang et al. 2019). The sandy soil displayed two strong diffraction peaks at 20.9° and 26.7°, which were assigned to the (100) and (101) crystal planes (Vijay et al. 2019). Similarly, CS-PE-SS40 composites exhibited the characteristic peaks of HDPE, SS, and CS, implying that the crystal structures of each component were not changed during the preparation procedure. The retainment of intrinsic properties of each component in CS-PE-SSx composites indicated that this materials preparation was feasible and non-destructive, which was promising in further applications such as flame retard.

Fig. 3. XRD curves of HDPE, sandy soil, cotton stalk, and CS-PE-SS40

SEM

Figure 4A through 4H showed the cross-section SEM images of CS-PE-SS0-40. Composites without SS exhibited that cotton stalk particles that were well combined with polyethylene matrix (Fig. 4A).

Fig. 4. Scanning electron micrographs of composites with different sandy soil contents (A through G); SEM image of sandy soil 40 wt% (H), EDS and mapping of silicon, oxygen, and carbon (I)

After adding SS, inorganic particles with diameters ranging from 10 µm to 110 µm were observed. The distribution of SS in polyethylene matrix became dense and uniform as their contents increased, indicating favorable adhesion of polyethylene on the surfaces of SS (Fig. 4B through 4G). In the amplified SEM image of CS-PE-SS40 composites, melt polymer matrix as fluid at high temperature tightly attached onto the surfaces of SS after cooling and showed no obvious cracks (Fig. 4H) (Essabir et al. 2017; Spoerk et al. 2017). The corresponding energy-dispersive X-ray spectrum and mapping further implied the presence and uniform distribution of SS in CS-PE-SS40 composites (Fig. 4I). The favorable combination in the interfaces and potential interactions between components were critical for the performance of functional composites. Thus, the well dispersion of SS in polymer matrix combined with the tight interface adhesion and interactions between SS and CS particles exhibited promising potential in the development of mechanical properties and thermal stabilities of CS-PE-SS40 composites.

Mechanical Properties of CS-PE-SSx

To study the impact of SS on the mechanical properties of CS-PE-SSx composites, the flexural strength, tensile strength, and impact strength of CS-PE-SS0, CS-PE-SS10, CS-PE-SS20, CS-PE-SS30, and CS-PE-SS40 composites were tested (Fig. 5). The mechanical strength, such as flexural strength, tensile strength, and impact strength, increased with more SS addition and reached values of 29.0 MPa, 15.8 MPa, and 3.17 kJ/m2 for CS-PE-SS40 composites, respectively (Figs. 5A through 5C). The improvement of mechanical properties of composites may be attributed to three reasons. Firstly, SS particles with high stiffness were well distributed in polymer matrix. They transferred stress efficiently and thus improved the mechanical properties of CS-PE-SSx composites (Chan et al. 2019). Secondly, the rigid SS particles embedded in polymer matrix may form a concentration of force when external forces were applied, thereby inducing crazing in the interface between SS and polyethylene matrix. Inorganic particles can prevent the development of crazing, and the increase of SS contents inhibits the growth of the number of crazing and improves the strength of the composites (Keskisaari et al. 2016). Lastly, the interacting forces between SS particles and CS powders also endowed composites favorable resistance to external forces and thus improved their mechanical properties. Overall, the composites fabricated with SS, CS, and PE were mechanically strong and suitable for functional wood-plastic plate materials.

 

Fig. 5. (A through C) Flexural strength, tensile strength, and impact strength, respectively, of composites with different sandy soil contents

Thermal Properties of CS-PE-SSx

The mass loss curves and mass loss derivatives of HDPE, LLDPE, CS, SS, CS-PE-SS0, CS-PE-SS5, CS-PE-SS10, CS-PE-SS15, CS-PE-SS20, CS-PE-SS30, and CS-PE-SS40 composites are presented in Fig. 6 to evaluate the effect of SS on the thermal stabilities of CS-PE-SSx composites. Both HDPE and LLDPE presented only one major step of thermal decomposition. The steps around 500 °C of HDPE and LLDPE were related to the break of carbon-carbon bond of the polymeric chains and formation of volatiles compounds (Moreno and Saron 2017). The main weight loss process of CS was around 350 °C, leading to 55% of weight loss, which was mainly caused by thermal depolymerization of the hemicellulose, breaking of glycosidic bond of the cellulose, and decomposition of the α-cellulose. Lignin in CS also started decomposition at approximately 500 °C (Guo et al. 2020). However, the thermogravimetric curve of SS exhibited only a weak peak between 630 °C and 770 °C, which can be attributed to the degradation of CaCO3 into CaO. It was noteworthy that CS-PE-SSx composites showed less mass loss compared with pure CS, HDPE, LDPE, and composites without SS. This may be due to the high thermal stability of SS and strong interacting forces with CS and fine dispersion in polymer matrix, which can prevent the penetration of volatile degradation products from the composites (Subramani et al. 2007; Koohestani et al. 2017). Furthermore, the temperature at 10% weight loss of CS-PE-SSx composites also increased from 252 °C of CS to 312 °C of CS-PE-SS40. All the results provided good evidence that the thermal stabilities of the composites were enhanced effectively.

Fig. 6. TG (A) and DTG (B) curves of SS, CS, LLDPE, HDPE, and CS-PE-SSx composites; the contents of SS were 0 wt%, 5 wt%, 10 wt%, 15 wt%, 20 wt%, 30 wt%, and 40 wt%, respectively.

Flame Retardant Properties of CS-PE-SSx

The SS, as an inorganic flame retardant, can effectively weaken the transfer of heat and the volatilization of combustible gas and reduce the contact area between combustible and air, making it difficult for the flame to continue to burn down, and finally improving the flame-retardant properties of the composites (Schirp and Su 2016; Zhang et al. 2017). In Fig. 7A, composites with different SS contents were ignited by flame lighter. It can be observed that when the composite sample only contained cotton stalk and polymer matrix, the flame became very bright after 10 s of ignition. While the composites with SS addition, it was difficult to ignite. Additionally, with the increase of SS contents, the flame intensity decreased obviously and was even unignited for CS-PE-SS40. The flame out time and burning distance were recorded after the tops of the samples were fully ignited (Fig. 7B through 7D). When the contents of SS were 0 wt%, the sample showed sustained combustion until it burned out. However, with the addition of SS, the samples exhibited obvious extinguishment phenomenon and the extinguishment time rapidly decreased (CS-PE-SS40 composites flamed out within 55 s). Compared with the composites without SS, the burning distance of the samples contained SS was remarkably shortened and an almost 75% decrease occurred with only 5 wt% SS addition.

The LOI value corresponds to the oxygen content required for combustion to occur, and a high limiting oxygen index value means high flame-retarded properties. (Zhou and Fu 2020). The LOI values of the composites were shown in Fig. 7E. When the proportion of SS was 0 wt%, the LOI values of the composite was 20.8%. The LOI values of the composites increased gradually with more SS usage. When the proportion of SS reached 40 wt%, the LOI value of the composite reached 24.1%. Many flame retardants, such as aluminum hydrogen phosphonate, triphenyl phosphate, ammonium polyphosphate, and so on, were applied to improve the flame-retardant abilities of wood-plastic composites, and their LOI values were calculated between approximately 18.1% and 26.6% (Altun et al. 2016; Pham et al. 2019; Yin et al. 2019). Thus, the CS-PE-SSx composites obtained from agricultural mulching film wastes were judged to be suitable for flame retard applications.

Fig. 7. The 10 s ignition test of the specimen (A), burning distance tests of the specimen (B), diagram of flame out time (C), diagram of burning extent (D), and LOI values of composites samples (E)

Feasibility Evaluation of the Materials Fabrication

To evaluate the feasibility of the authors’ management on agricultural wastes, soil from Xinjiang, Shandong, and Jiangsu were selected to composite with waste mulching film and cotton stalk. The results showed that all the agricultural wastes used can form intact composites with promising properties (Fig. 8A). The flexural strength, tensile strength, and impact strength of the three composites were relatively lower than the commercial wood-plastic composites, but still suitable for applications in plates fields (Hyvärinen et al. 2014). The LOI values of the composites with different soil from three regions were approximately 23.5%, which was higher than that of the sample without soil. These results indicated that the conversion of agricultural wastes into flame retardant materials was feasible, and the waste soil acts as a flame retardant in the composites was of noticeable importance for the authors to develop an efficient and economical strategy to utilize the waste resources.

Fig. 8. (A) Soil acquired in different provinces of China and the photographs of corresponding composites; (B) Mechanical properties; and (C) LOI values of the composites fabricated using agricultural mulching film wastes from Shandong, Jiangsu, and Xinjiang province of China

CONCLUSIONS

  1. Simple compounding and injection molding procedures were applied to convert plastic agriculture mulching film wastes into functional flame-retarded composites directly. The added sandy soil particles were uniformly dispersed in the polymer matrix and showed promising interface combination.
  2. The resultant composites showed a flexural strength of approximately 29.0 MPa, a tensile strength approximately 15.8 MPa, an impact strength of approximately 3.17 kJ/m2 and improved thermal stabilities.
  3. The addition of sandy soil particles endowed materials favorable flame-retarded properties, which can resistant to fire ignition and flame out within 55 s.

ACKNOWLEDGMENTS

The authors are grateful for the support of the financial support of the National Key Research and Development Program of China (No. 2018YFD1101001); the distinguished expert of Taishan scholars Shandong province project and the higher education superior discipline team training program of Shandong province.

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Article submitted: November 10, 2020; Peer review completed: February 6, 2021; Revised version received and accepted; February 21, 2021; Published: February 26, 2021.

DOI: 10.15376/biores.16.2.2838-2852