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Hybrid green organic/inorganic filler polypropylene composites: Morphological study and mechanical performance investigations

  • Mohammed T. Hayajneh ORCID logo EMAIL logo , Faris M. AL-Oqla ORCID logo and Mu’ayyad M. Al-Shrida ORCID logo
Published/Copyright: September 22, 2021
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Abstract

In this study, the morphological and mechanical performances of hybrid green organic and inorganic filler composites were investigated. Various hybrid reinforcements using natural waste fillers including lemon leaves and eggshells were utilized for the study. The tensile strength, tensile modulus, elongation to break, flexural strength, and flexural modulus were investigated for the composites with polypropylene matrix. The results revealed that eggshells composites had the best values for both tensile and flexural tests while lemon leaves composites had the lowest values. However, the hybrid filler (lemon leaves-eggshells) had intermediate values. The poor properties of lemon leaves were attributed to the agglomeration and weak bonding presented by the morphological analysis of the hybrid composites.

1 Introduction

In recent decades, synthetic polymers have become a strong competitor to metals in different industries, ranging from infrastructure to aerospace applications due to its lightness and corrosion resistance (1). Despite these properties, they had a negative environmental impact as the annual waste of plastics was estimated to exceed 300 million tons in 2015. This produces a vast amount of CO2 and other poisonous elements during degradation (2,3). Therefore, researchers around the world have been turning toward bio-polymeric composites (bio-filler reinforced synthetic polymer matrix or bio/synthetic filler reinforced bio-polymer matrix) to reduce the harmful effects of synthetic polymer on the environment. Among bio-polymeric composites, natural fabric composites have aroused great interest due to their internal natural fibers that exhibit good properties such as availability, lightness, low cost, and good mechanical, thermal, and electrical properties along with the most important quality of biodegradability (4,5,6,7).

Diverse types of single and hybrid natural fibers like corn silk/Hibiscus cannabinus (8), waste tea leaves (9), olive leaves (10,11), Jordanian natural fiber species (12,13), sweet lime and lemon (14), and rice husk (15) have been fabricated with various polymer matrices. In addition to the organic natural fibers, inorganic fillers like glass fiber, carbon fiber, calcium carbonate, fly ash, etc., can also be used to reinforce polypropylene (PP) (16). Among inorganic fillers, eggshells (Es) can be a candidate to reinforce PP due to its characteristics like thermal stability, low price, availability, and user friendliness (17,18).

The advantages of PP, such as thermal stability, lightweight, relative low cost of processing, recyclability, and resistance to harsh conditions (19), make it one of the most common candidates for use as a matrix. On the other hand, PP suffers from low strength and modulus and low thermal conductivity (20). Consequently, engineers have been struggling to improve the mechanical, thermal, and tribological properties of the PP matrix by incorporating different organic and/or inorganic fillers (6,19,21,22). However, the effects of hybrid organic–inorganic reinforcement on the mechanical and thermal properties of PP have not been fully explored. So, the current study is trying to predict the mechanical characteristics (modulus and strength) and demonstrate that such fillers would be thermally stable during the manufacturing process of embedding PP with hybrid organic–inorganic reinforcement containing different percentages of lemon leaves fiber and Es reinforcement.

2 Materials and methods

2.1 Materials

In this study, virgin PP was used as matrix in the form of granules. It was provided from SABIC-Saudi Arabia (density = 0.9 g·cm−3, thermal conductivity = 0.26 W·(m·K)−1.

The organic filler lemon leaves were used as the first filler in the PP matrix. No treatments were conducted on the lemon leaves to enhance its properties before utilizing it as a raw material in such composite materials. They were taken as it is from Jordanian lemon trees. The preparation of lemon leaves passed through many steps. The first step was the collection and cutting of the leaves from a local tree, as seen in Figure 1a. Second, the fibers were chopped into small pieces by scissors as shown in Figure 1b. Third, the leaves were placed into a blender converting them into lemon (L) leaves fiber containing midrib, lamina, and vein as revealed in Figure 1c and d, and eventually, a random sample of 35 midribs and 35 laminas were selected to calculate the average and standard deviation of their lengths as shown in Figure 1e and f. The mean and standard deviation of the midribs were 21 ± 13.4 mm while the mean and standard deviation of the laminas were approximately 6 ± 4.5 mm. The density of the entire L is 0.78 g·cm−3 as calculated from the Archimedes rule. The surface morphology of L fiber was investigated by using a scanning electron microscope (SEM) in Section 3.3.

Figure 1 
                  Preparation of the lemon fiber: (a) collecting lemon leaves, (b) chopping by scissors, (c) chopping by blender blades, (d) pile of midribs and laminas of lemon leaves, (e) measuring the approximate length of midribs, and (f) laminas by ruler.
Figure 1

Preparation of the lemon fiber: (a) collecting lemon leaves, (b) chopping by scissors, (c) chopping by blender blades, (d) pile of midribs and laminas of lemon leaves, (e) measuring the approximate length of midribs, and (f) laminas by ruler.

Es, an inorganic filler, were used as the second filler without any treatments in the PP matrix. The green waste Es is considered as an inorganic filler because 95% of it is composed of calcium carbonate (23). The shells were gathered from various bakeries. Then, they were sprayed with water to clean the remnants of yolks and albumen. After that, the shells were dried in the sun and broken into small flakes. Finally, a random small pile of 35 flakes of the shells was taken to find the close length of the shells’ fragments. The mean and standard deviation were 3.6 and 1.5 mm, respectively. The density was measured in our previous studies (17,18) and it was 2.5 g·cm−3. Figure 2 displays the various stages of preparing the shells. The topography of Es is presented in Section 3.3.

Figure 2 
                  The stages of shells’ preparation including (a) gathering, (b) flaking, and (c) measuring the length of the shells by ruler.
Figure 2

The stages of shells’ preparation including (a) gathering, (b) flaking, and (c) measuring the length of the shells by ruler.

2.2 Composite processing

Mono composite and hybrid composite were prepared using the three weight percentages of the fillers (5, 10, and 20 wt%) of L, Es, and H (50 wt% of L and 50 wt% of Es). First, the compound of the matrix and the filler was mixed manually. Then, the compound was placed into a locally manufactured single-screw extruder. Finally, the extruded mixtures were compressed by four tones at room temperature in a rectangular mold with the dimensions of 100 mm × 70 mm × 5 mm. The output zone temperature of the extruder was in the range of 200–220°C. The weight percentages and the codes of the composites are presented in Table 1.

Table 1

The codes and weight percentages of the composites

Sample code L (wt%) Es (wt%) PP (wt%)
PP 0 0 100
5 L–PP 5 0 95
10 L–PP 10 0 90
20 L–PP 20 0 80
5 Es–PP 0 5 95
10 Es–PP 0 10 90
20 Es–PP 0 20 80
5 H–PP 2.5 2.5 95
10 H–PP 5 5 90
20 H–PP 10 10 80

2.3 Tensile test

The tensile properties like tensile strength, modulus of elasticity, and elongation at break were determined according to the ASTM D3039-3039M at a crosshead speed of 2 mm·min−1. The test was performed in a uniaxial direction on a universal testing machine (UTM; model WDW-20). The dimensions of the samples were 80 mm × 20 mm × 5 mm with a gauge length of 50 mm.

2.4 Flexural test

A three-point bending test was used to determine the flexural strength, which represents the highest flexural stress on the stress–strain curve, and the flexural modulus ( E f ) which can be calculated from the ratio of flexural stress ( σ f ) to flexural strain ( ε f ) within the elastic region. Flexural stress, flexural strain, and flexural modulus were calculated according to the Eqs. 13, respectively. The test was performed on a UTM (model WDW-20) according to ASTM D790 at room temperature with a crosshead speed of 2 mm·min−1. Rectangular specimens were cut from the original sheets with dimensions of 100 mm × 10 mm × 5 mm.

(1) σ f = 3 F L 2 W T 2

where σ f and F represent the flexural stress (in MPa) and the applied force (in N), while W, T, and L represent the width (in mm), the thickness (in mm), and support span (in mm), respectively.

(2) ε f = 6 D T L 2

where ε f is the flexural strain and D is the maximum deflection at the center of the specimen in mm. T and L are the thickness and the support span in mm.

(3) E f = Δ σ f Δ ε f

2.5 Scanning electron microscope characterization

A SEM (Quanta™ 450 FEG SEM) was used to investigate the distribution of fiber in the matrix, pull-out phenomenon, and the bonding at the matrix–fiber interface after the tensile test. Also, the morphology of the raw fibers was characterized by SEM. All samples were sputtered with a gold layer of 18 nm prior to SEM examination to avoid electrostatic charging.

3 Results and discussion

3.1 Tensile test

3.1.1 Tensile modulus

The tensile modulus of elasticity for mono composites (L–PP or Es–PP) and hybrid composites (H–PP) are presented in Figure 3. It is evident from the figure that L filler improves the modulus value of PP at 5 L wt%. At 10 L wt%, unlike 10 Es and 10 H wt%, the modulus value dropped significantly to reach the lowest value among all samples. At 20 L wt% the tensile modulus increased again to reach the neat value. This trend may be attributed to stress concentration. The addition of an insufficient amount of filler leads to stress concentration, which speeds up the failure process in the composite. The inadequate amount does not allow the reinforcement to do its main function, that is, resisting the external load. At 5 L wt%, the stress concentration is very small, and the fibers partially do their role which leads to initial improvement. However, at 10 L wt%, the stress concentration increased, leading to lower modulus. At 20 wt%, it sounds that the L fibers begin to withstand the external forces which may explain the improvement of modulus. Similar results were obtained by Zanini et al. (24) for palm fiber–PP composites.

Figure 3 
                     The tensile modulus values of mono and hybrid composites.
Figure 3

The tensile modulus values of mono and hybrid composites.

According to Es–PP composites, a different trend is observed. The tensile modulus at 5 Es wt% increased by 15%, whereas at 10 Es wt% the tensile modulus touches the highest value to reach an improvement of 21%. Nevertheless, at 20 Es wt%, the modulus diminished again, but it is still higher than the tensile modulus of neat PP. The improvement of moduli at 5 and 10 wt% of Es refers to the nature of stiff bio-filler Es where the stiffness property indicates the modulus. On the other hand, the decline in tensile modulus at 20 Es wt% may refer to the agglomerates that are presented later in Section 3.3.2. A similar trend was reported by Ghabeer et al. (25).

The behavior of H-composites differs from L and Es composites, where the tensile modulus decreased gradually while increasing the weight percentage of H filler. Despite this decline, the moduli of H-composites exceeded PP modulus, and achieved the highest improvement of 19% at 5 H wt%.

The L composites achieved the lowest values when compared to Es and H composites. The cause behind this might be the poor bonding at the L–PP interface. Not only that, the agglomeration phenomenon due to poor mixing may contribute to the aforementioned result. This interpretation is presented by SEM in Section 3.3.

3.1.2 Tensile strength

Figure 4 displays the tensile strength for all composites (L–PP, Es–PP, and H–PP). It is conspicuous that all types of composites have lower tensile strength than neat PP. The group of L composites shows the same trend that is observed in tensile modulus but with lower values. The tensile strength diminished to reach the lowest value at 10 L wt% among all composites and again increased at 20 L wt%. The same interpretation that was used in tensile modulus for this trend may be valid here. In addition to that, the decrease in tensile strength in L–PP composites below the tensile strength of PP can be attributed to the weak adhesion between L fiber and PP matrix which facilitates the pull-out phenomenon leading to hastening the failure of the composite and therefore reducing the tensile value. On top of that, the agglomeration of L fiber prevents matrix–matrix contact and causes an internal weak mesh prompting faster failure. This is displayed by SEM micrographs. Ghabeer et al. (25) recorded very similar observations.

Figure 4 
                     The tensile strength values of mono and hybrid composites.
Figure 4

The tensile strength values of mono and hybrid composites.

Although the Es composites do not reach the tensile strength of neat PP, they get better results when compared to L composites. It is expected that Es reduce the tensile strength of PP because of the nature of stiff bio-ceramic Es. Also, better results may refer to lower agglomeration of Es in the PP matrix, since the density of Es is relatively high when compared to L and thus the lower volume of Es filler. Further, the relative improvement can be attributed to better adhesion between Es and PP as explained in Section 3.3.

The addition of hybrid filler (Es + L) also reduces the tensile strength of PP as shown in Figure 4. The 5 and 10 wt% of fillers give a very close tensile strength value that dropped significantly at 20 wt% due to agglomeration.

3.1.3 Elongation at break

It is evident from Figure 5 that the elongation at break for all composites diminished generally with the increasing weight percentage of fillers regardless of the type of filler. Actually, such a trend is forecasted since the addition of fillers makes the matrix brittle. The trend of elongation at break matches the trend of tensile strength with different values. The elongation at break value of 0.2% for PP is also reported by Kumar et al. (26).

Figure 5 
                     The elongation at break values for all composites.
Figure 5

The elongation at break values for all composites.

3.1.4 Stress–strain behavior

The tensile stress–strain behavior of the five replicates of five L–PP composites is depicted in Figure 6. It is demonstrated from the replicates in the figure that the variations of tensile strength are marginal where the standard deviation did not exceed 1.6 MPa. However, the variation within the tensile moduli and elongations at break is higher than that presented within the tensile strength. This variation is expected due to the random orientation of the fillers inside the matrix that may cause some fiber agglomeration leading to poor fiber distribution and lower adhesion with the matrix. Thus, several replicates were considered according to the standard tensile test, and the average values were considered. An irregular behavior at the birth of the curve is detected in all replicates. This may be associated with the sample slipping during the beginning of load applying.

Figure 6 
                     Stress–strain behavior of five replicates of five L–PP composite.
Figure 6

Stress–strain behavior of five replicates of five L–PP composite.

3.2 Flexural test

The results of flexural modulus and flexural strength of L, Es, and H composites are depicted in Figures 7 and 8, respectively. Figure 7 presents that all levels (5, 10, and 20 wt%) of reinforcements improved the flexural modulus regardless of the type of filler except at 20 L wt% which adversely affected the flexural modulus where it worsened the flexural modulus of neat PP. The improvement of flexural modulus may be attributed to the used stiff fillers, while the flexural modulus dropping at 20 L wt% may refer to the high fiber–fiber interactions due to the dispersion problem of natural L as presented in the SEM micrograph (Section 3.3.2). The decrease in the flexural modulus at high weight percentage was reported by Arib et al. (18) for the pineapple leaf–PP composite. Figure 7 also shows that all Es composites have the highest values of flexural modulus compared to L and H composites. The flexural modulus reaches the vertex at 20 Es wt% where it was improved by 34%.

Figure 7 
                  The flexural modulus values of mono and hybrid composites.
Figure 7

The flexural modulus values of mono and hybrid composites.

Figure 8 
                  The flexural strength values of mono and hybrid composites.
Figure 8

The flexural strength values of mono and hybrid composites.

In the case of L composites, the flexural moduli are generally lower than those in the Es composites. This may be due to numerous causes. First, the poor bonding at the L–PP interface. Second, the agglomeration of L fiber may occur due to the poor mixing condition and the higher cross-sectional areas of L which hinder the dispersion of L in the PP matrix (27). The aforementioned problems will be discussed in Section 3.3.2.

According to Figure 8, it can be observed that the flexural strength of Es composites has the highest values among the other fillers (L and H) despite the fact that they did not touch the strength of neat PP. At 20 wt% of the three types of fillers, the composites get the lowest values. This might be due to the reason discussed before. Kumar et al. (26) recorded an increase in flexural modulus from 1,300 MPa for PP to 1,426 MPa for PP with 20 wt% of Es.

For the composites with H filler, they get approximately intermediate values between Es and L composites for flexural and tensile strength. Actually, this will be rational if the rule of mixture is applied. Although the results of flexural and tensile tests are similar, the flexural test gave better results when compared to the tensile test because in the flexural test only the central part of the sample is affected by load, while in the tensile test the whole sample is exposed to load. Therefore, if the void is not in the center, its contribution will be insignificant in the fracture (7).

3.3 Morphological analysis

3.3.1 The surface morphology of fiber

The morphology of the midrib and lamina of the lemon leaf was investigated by SEM as shown in Figures 9 and 10, respectively. It could be observed from Figures 9 and 10 that there is a significant amount of impurities on the surface of the midrib (Figure 9) and lamina (Figure 10) fiber because no attempt was made to treat or even clean the fiber. Furthermore, no pits are observed on the surface of the fiber, midrib, and lamina, which indicate the existence of the waxy layer and lignin (28).The waxy layer, impurities, and smooth surface may have a role in the weak bonding with PP which results in poorer mechanical properties compared to Es filler. Moreover, it can be found that the midrib and lamina have different topography which may lead to different bonding behavior.

Figure 9 
                     SEM micrograph of lemon leaf midrib: micrograph (b) is a magnification for the yellow square in micrograph (a).
Figure 9

SEM micrograph of lemon leaf midrib: micrograph (b) is a magnification for the yellow square in micrograph (a).

Figure 10 
                     SEM micrograph of a small flake of lemon leaf (lamina and veins): micrograph (b) is a magnification for the yellow square in micrograph (a).
Figure 10

SEM micrograph of a small flake of lemon leaf (lamina and veins): micrograph (b) is a magnification for the yellow square in micrograph (a).

Figure 11 presents the morphology of the outer surface of Es flake. It can be observed that the impurities on the surface of the shell are actually lower than that in L fiber. Also, the interconnected porosity shown in Figure 11 refers to the nature of porous Es. The lower impurities and the rougher surface of Es may have a positive impact on bonding behavior.

Figure 11 
                     SEM micrograph of the outer surface of Es flake: micrograph (b) is a magnification for the yellow square in micrograph (a).
Figure 11

SEM micrograph of the outer surface of Es flake: micrograph (b) is a magnification for the yellow square in micrograph (a).

3.3.2 The surface morphology of fractured composites

The microstructure of fractured composites (20 Es–PP and 20 L–PP) after the tensile test was investigated by SEM, is shown in Figures 12 and 13. It can be seen from Figure 12a that the distribution of Es flakes though PP matrix is almost good, and the agglomerates found in the Es composite are lower than that in L composite as seen in Figure 13b. The agglomeration facilitates the pull-out phenomenon because there is no matrix to hold the fiber (Figure 12c) speeding up the failure process which in turn interprets the significant reduction in tensile strength and modulus at 20 wt%. Furthermore, Figure 12c shows good bonding at the interface between PP and Es. Figure 12b also shows a transverse cross-section of Es flake. So, the thickness used in the flake can be measured.

Figure 12 
                     SEM micrograph of 20 Es–PP composite: micrograph (b) is a magnification for the first square in micrograph (a) and micrograph (c) is a magnification for the second square in micrograph (a).
Figure 12

SEM micrograph of 20 Es–PP composite: micrograph (b) is a magnification for the first square in micrograph (a) and micrograph (c) is a magnification for the second square in micrograph (a).

Figure 13 
                     SEM micrograph of 20 Es–PP composite: micrograph (b) is a magnification for the yellow square in micrograph (a). Yellow arrows in micrograph (a) indicate pull-out.
Figure 13

SEM micrograph of 20 Es–PP composite: micrograph (b) is a magnification for the yellow square in micrograph (a). Yellow arrows in micrograph (a) indicate pull-out.

Figure 13b clears the poor bonding between L fiber and PP matrix. However, Figure 13a shows a large number of pull-outs of L fiber which might make the tensile and flexural values of 20 L–PP composites lower than the tensile and flexural values of 20 Es–PP. If Figure 13a is compared with Figure 12a, it will be easy to note that the number of pull-outs in L composite is much higher than that in the Es composite.

4 Conclusion

Green Es and hybrid fillers had positive effects on the flexural and tensile modulus of neat PP regardless of weight percentages, but lemon filler worsened both flexural and tensile modulus at specific weight percentages. On the other hand, all fillers reduced the values of tensile strength and flexural strength of PP. In any case, the hybrid filler obtained in-between results compared to lemon and Es fillers. Moreover, it can be revealed that Es are better than lemon leaves in all mechanical properties at all percentages. Furthermore, it can be noted that 20 wt% of H and Es filler reduced the tensile and flexural strength. It may refer to the agglomeration of fiber in the PP matrix as shown in SEM images.

  1. Funding information: This work was supported by a grant from the Deanship of Scientific Research at the Jordan University of Science and Technology (JUST) with Grant no. 448/2019.

  2. Author contributions: The manuscript was written with the contributions of all authors. All authors have given approval to the final version of the manuscript.

  3. Conflict of interest: Authors state no conflict of interest.

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Received: 2021-07-01
Revised: 2021-08-12
Accepted: 2021-08-17
Published Online: 2021-09-22

© 2021 Mohammed T. Hayajneh et al., published by De Gruyter

This work is licensed under the Creative Commons Attribution 4.0 International License.

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  22. Fabrication and characterization of thermoresponsive composite carriers: PNIPAAm-grafted glass spheres
  23. Effect of talc and diatomite on compatible, morphological, and mechanical behavior of PLA/PBAT blends
  24. Multifunctional graphene nanofiller in flame retarded polybutadiene/chloroprene/carbon black composites
  25. Strain-dependent wicking behavior of cotton/lycra elastic woven fabric for sportswear
  26. Enhanced dielectric properties and breakdown strength of polymer/carbon nanotube composites by coating an SrTiO3 layer
  27. Analysis of effect of modification of silica and carbon black co-filled rubber composite on mechanical properties
  28. Polytriazole resins toughened by an azide-terminated polyhedral oligomeric silsesquioxane (OADTP)
  29. Phosphine oxide for reducing flammability of ethylene-vinyl-acetate copolymer
  30. Study on preparation and properties of bentonite-modified epoxy sheet molding compound
  31. Polyhedral oligomeric silsesquioxane (POSS)-modified phenolic resin: Synthesis and anti-oxidation properties
  32. Study on structure and properties of natural indigo spun-dyed viscose fiber
  33. Biodegradable thermoplastic copolyester elastomers: Methyl branched PBAmT
  34. Investigations of polyethylene of raised temperature resistance service performance using autoclave test under sour medium conditions
  35. Investigation of corrosion and thermal behavior of PU–PDMS-coated AISI 316L
  36. Modification of sodium bicarbonate and its effect on foaming behavior of polypropylene
  37. Effect of coupling agents on the olive pomace-filled polypropylene composite
  38. High strength and conductive hydrogel with fully interpenetrated structure from alginate and acrylamide
  39. Removal of methylene blue in water by electrospun PAN/β-CD nanofibre membrane
  40. Theoretical and experimental studies on the fabrication of cylindrical-electrode-assisted solution blowing spinning nanofibers
  41. Influence of l-quebrachitol on the properties of centrifuged natural rubber
  42. Ultrasonic-modified montmorillonite uniting ethylene glycol diglycidyl ether to reinforce protein-based composite films
  43. Experimental study on the dissolution of supercritical CO2 in PS under different agitators
  44. Experimental research on the performance of the thermal-reflective coatings with liquid silicone rubber for pavement applications
  45. Study on controlling nicotine release from snus by the SIPN membranes
  46. Catalase biosensor based on the PAni/cMWCNT support for peroxide sensing
  47. Synthesis and characterization of different soybean oil-based polyols with fatty alcohol and aromatic alcohol
  48. Molecularly imprinted electrospun fiber membrane for colorimetric detection of hexanoic acid
  49. Poly(propylene carbonate) networks with excellent properties: Terpolymerization of carbon dioxide, propylene oxide, and 4,4ʹ-(hexafluoroisopropylidene) diphthalic anhydride
  50. Polypropylene/graphene nanoplatelets nanocomposites with high conductivity via solid-state shear mixing
  51. Mechanical properties of fiber-reinforced asphalt concrete: Finite element simulation and experimental study
  52. Applying design of experiments (DoE) on the properties of buccal film for nicotine delivery
  53. Preparation and characterizations of antibacterial–antioxidant film from soy protein isolate incorporated with mangosteen peel extract
  54. Preparation and adsorption properties of Ni(ii) ion-imprinted polymers based on synthesized novel functional monomer
  55. Rare-earth doped radioluminescent hydrogel as a potential phantom material for 3D gel dosimeter
  56. Effects of cryogenic treatment and interface modifications of basalt fibre on the mechanical properties of hybrid fibre-reinforced composites
  57. Stable super-hydrophobic and comfort PDMS-coated polyester fabric
  58. Impact of a nanomixture of carbon black and clay on the mechanical properties of a series of irradiated natural rubber/butyl rubber blend
  59. Preparation and characterization of a novel composite membrane of natural silk fiber/nano-hydroxyapatite/chitosan for guided bone tissue regeneration
  60. Study on the thermal properties and insulation resistance of epoxy resin modified by hexagonal boron nitride
  61. A new method for plugging the dominant seepage channel after polymer flooding and its mechanism: Fracturing–seepage–plugging
  62. Analysis of the rheological property and crystallization behavior of polylactic acid (Ingeo™ Biopolymer 4032D) at different process temperatures
  63. Hybrid green organic/inorganic filler polypropylene composites: Morphological study and mechanical performance investigations
  64. In situ polymerization of PEDOT:PSS films based on EMI-TFSI and the analysis of electrochromic performance
  65. Effect of laser irradiation on morphology and dielectric properties of quartz fiber reinforced epoxy resin composite
  66. The optimization of Carreau model and rheological behavior of alumina/linear low-density polyethylene composites with different alumina content and diameter
  67. Properties of polyurethane foam with fourth-generation blowing agent
  68. Hydrophobicity and corrosion resistance of waterborne fluorinated acrylate/silica nanocomposite coatings
  69. Investigation on in situ silica dispersed in natural rubber latex matrix combined with spray sputtering technology
  70. The degradable time evaluation of degradable polymer film in agriculture based on polyethylene film experiments
  71. Improving mechanical and water vapor barrier properties of the parylene C film by UV-curable polyurethane acrylate coating
  72. Thermal conductivity of silicone elastomer with a porous alumina continuum
  73. Copolymerization of CO2, propylene oxide, and itaconic anhydride with double metal cyanide complex catalyst to form crosslinked polypropylene carbonate
  74. Combining good dispersion with tailored charge trapping in nanodielectrics by hybrid functionalization of silica
  75. Thermosensitive hydrogel for in situ-controlled methotrexate delivery
  76. Analysis of the aging mechanism and life evaluation of elastomers in simulated proton exchange membrane fuel cell environments
  77. The crystallization and mechanical properties of poly(4-methyl-1-pentene) hard elastic film with different melt draw ratios
  78. Review Articles
  79. Aromatic polyamide nonporous membranes for gas separation application
  80. Optical elements from 3D printed polymers
  81. Evidence for bicomponent fibers: A review
  82. Mapping the scientific research on the ionizing radiation impacts on polymers (1975–2019)
  83. Recent advances in compatibility and toughness of poly(lactic acid)/poly(butylene succinate) blends
  84. Topical Issue: (Micro)plastics pollution - Knowns and unknows (Guest Editor: João Pinto da Costa)
  85. Simple pyrolysis of polystyrene into valuable chemicals
  86. Topical Issue: Recent advances of chitosan- and cellulose-based materials: From production to application (Guest Editor: Marc Delgado-Aguilar)
  87. In situ photo-crosslinking hydrogel with rapid healing, antibacterial, and hemostatic activities
  88. A novel CT contrast agent for intestinal-targeted imaging through rectal administration
  89. Properties and applications of cellulose regenerated from cellulose/imidazolium-based ionic liquid/co-solvent solutions: A short review
  90. Towards the use of acrylic acid graft-copolymerized plant biofiber in sustainable fortified composites: Manufacturing and characterization
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