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The neutron- and X-ray-shielding, morphological, physical, mechanical, and self-healing properties were investigated for natural rubber (NR) composites containing varying gadolinium oxide (Gd2O3) contents (0, 25, 50, 75, and 100 parts per hundred parts of rubber; phr) to investigate their potential uses as self-healing and flexible neutron- and X-ray-shielding materials. Gd2O3 was selected as a radiation protective filler in this work due to its preferable properties of having relatively high neutron absorption cross-section (σabs), atomic number (Z), and density (ρ) that could potentially enhance interaction probabilities with incident radiation. The results indicated that the overall neutron-shielding and X-ray-shielding properties of the NR composites were enhanced with the addition of Gd2O3, as evidenced by considerable reductions in the half-value layer (HVL) values of the samples containing 100 phr Gd2O3 to just 1.9 mm and 1.3 mm for thermal neutrons and 60 kV X-rays, respectively. Furthermore, the results revealed that, with the increase in Gd2O3 content, the mean values (± standard deviations) of the tensile strength and elongation at break of the NR composites decreased, whereas the hardness (Shore A) increased, for which extreme values were found in the sample with 100 phr Gd2O3 (3.34 ± 0.26 MPa, 411 ± 9%, and 50 ± 1, respectively). In order to determine the self-healing properties of the NR composites, the surfaces of the cut samples were gently pressed together, and they remained in contact for 60 min; then, the self-healing properties (the recoverable strength and the %Recovery) of the self-healed samples were measured, which were in the ranges of 0.30–0.40 MPa and 3.7–9.4%, respectively, for all the samples. These findings confirmed the ability to autonomously self-heal damaged surfaces through the generation of a reversible ionic supramolecular network. In summary, the outcomes from this work suggested that the developed Gd2O3/NR composites have great potential to be utilized as effective shielding materials, with additional dual shielding and self-healing capabilities that could prolong the lifetime of the materials, reduce the associated costs of repairing or replacing damaged equipment, and enhance the safety of all users and the public. [ABSTRACT FROM AUTHOR]

Although natural rubber was regarded as biodegradable, the degradation is a time-consuming process that could take weeks or months for any degradation or substantial weight loss to be observable, resulting in the need for novel processes/methods to accelerate the rubber degradation. As a result, this work investigated the potential utilization of chitosan (CS) as a biodegradation enhancer for radiation-vulcanized natural rubber latex (R-VNRL) and hybrid radiation and peroxide-vulcanized natural rubber latex (RP-VNRL) composites, with varying CS contents (0, 2, 4, or 6 phr). The R-VNRL samples were prepared using 15 kGy gamma irradiation, while the RP-VNRL samples were prepared using a combination of 0.1 phr tert-butyl hydroperoxide (t-BHPO) and 10 kGy gamma irradiation. The properties investigated were biodegradability in the soil and the morphological, chemical, mechanical, and physical properties, both before and after undergoing thermal aging. The results indicated that the biodegradability of both the R-VNRL and RP-VNRL composites was enhanced with the addition of CS, as evidenced by increases in the percentage weight loss (% weight loss) after being buried in soil for 8 weeks from 6.5 ± 0.1% and 6.4 ± 0.1% in a pristine R-VNRL and RP-VNRL samples, respectively, to 10.5 ± 0.1% and 10.2 ± 0.1% in 6-pph CS/R-VNRL and 6-pph CS/RP-VNRL composites, respectively, indicating the biodegradation enhancement of approximately 60%. In addition, the results revealed that the addition of CS could increase the value of tensile modulus by 119%, while decrease the values of tensile strength and elongation at break by 50% and 43%, respectively, in the specimens containing 6-phr CS. In terms of the color appearances, the samples were lighter and yellower after the addition of CS, as evidenced by the noticeably increased L* and b* values, based on the CIE L*a*b* color space system. Furthermore, the investigation into the effects of thermal aging showed that the overall tensile properties for both curing systems were reduced, while varying degrees of color change were observed, with the pristine R-VNRL and RP-VNRL samples having more pronounced degradation/changes for both properties. In conclusion, the overall results suggested that CS had great potential to be applied as a bio-filler in R-VNRL and RP-VNRL composites to effectively promote the biodegradability, environmental friendliness, and resistance to thermal degradation of the composites. [ABSTRACT FROM AUTHOR]

The potential utilization of wood/polyvinyl chloride (WPVC) composites containing an X-ray protective filler, namely bismuth oxide (Bi2O3) particles, was investigated as novel, safe, and environmentally friendly X-ray shielding materials. The wood and Bi2O3 contents used in this work varied from 20 to 40 parts per hundred parts of PVC by weight (pph) and from 0 to 25, 50, 75, and 100 pph, respectively. The study considered X-ray shielding, mechanical, density, water absorption, and morphological properties. The results showed that the overall X-ray shielding parameters, namely the linear attenuation coefficient (µ), mass attenuation coefficient (µm), and lead equivalent thickness (Pbeq), of the WPVC composites increased with increasing Bi2O3 contents but slightly decreased at higher wood contents (40 pph). Furthermore, comparative Pbeq values between the wood/PVC composites and similar commercial X-ray shielding boards indicated that the recommended Bi2O3 contents for the 20 pph (40 ph) wood/PVC composites were 35, 85, and 40 pph (40, 100, and 45 pph) for the attenuation of 60, 100, and 150-kV X-rays, respectively. In addition, the increased Bi2O3 contents in the WPVC composites enhanced the Izod impact strength, hardness (Shore D), and density, but reduced water absorption. On the other hand, the increased wood contents increased the impact strength, hardness (Shore D), and water absorption but lowered the density of the composites. The overall results suggested that the developed WPVC composites had great potential to be used as effective X-ray shielding materials with Bi2O3 acting as a suitable X-ray protective filler. [ABSTRACT FROM AUTHOR]

This work theoretically determined the high-energy photon shielding properties of high-density polyethylene (HDPE) composites containing rare-earth oxides, namely samarium oxide (Sm2O3), europium oxide (Eu2O3), and gadolinium oxide (Gd2O3), for potential use as lead-free X-ray-shielding and gamma-shielding materials using the XCOM software package. The considered properties were the mass attenuation coefficient (µm), linear attenuation coefficient (µ), half value layer (HVL), and lead equivalence (Pbeq) that were investigated at varying photon energies (0.001–5 MeV) and filler contents (0–60 wt.%). The results were in good agreement (less than 2% differences) with other available programs (Phy-X/PSD) and Monte Carlo particle transport simulation code, namely PHITS, which showed that the overall high-energy photon shielding abilities of the composites considerably increased with increasing rare-earth oxide contents but reduced with increasing photon energies. In particular, the Gd2O3/HDPE composites had the highest µm values at photon energies of 0.1, 0.5, and 5 MeV, due to having the highest atomic number (Z). Furthermore, the Pbeq determination of the composites within the X-ray energy ranges indicated that the 10 mm thick samples with filler contents of 40 wt.% and 50 wt.% had Pbeq values greater than the minimum requirements for shielding materials used in general diagnostic X-ray rooms and computerized tomography rooms, which required Pbeq values of at least 1.0 and 1.5 mmPb, respectively. In addition, the comparisons of µm, µ, and HVL among the rare-earth oxide/HDPE composites investigated in this work and other lead-free X-ray shielding composites revealed that the materials developed in this work exhibited comparable X-ray shielding properties in comparison with that of the latter, implying great potential to be used as effective X-ray shielding materials in actual applications. [ABSTRACT FROM AUTHOR]

This work aimed to theoretically determine the high-energy-photon-shielding properties of flexible wood/natural rubber (NR) and NR composites containing photon protective fillers, namely Pb, Bi2O3, or Bi2S3, using XCOM. The properties investigated were the mass attenuation coefficient (µm), linear attenuation coefficient (µ), and half value layer (HVL) of the composites, determined at varying photon energies of 0.001–5 MeV and varying filler contents of 0–1000 parts per hundred parts of rubber by weight (phr). The simulated results, which were in good agreement with previously reported experimental values (average difference was 5.3%), indicated that overall shielding properties increased with increasing filler contents but decreased with increasing incident photon energies. The results implied the potential of bismuth compounds, especially Bi2O3, to replace effective but highly toxic Pb as a safer high-energy-photon protective filler, evidenced by just a slight reduction in µm values compared with Pb fillers at the same filler content and photon energy. Furthermore, the results suggested that the addition of 20 phr wood particles, primarily aimed to enhance the rigidity and dimensional stability of Pb/NR, Bi2O3/NR, and Bi2S3/NR composites, did not greatly reduce shielding abilities; hence, they could be used as dimensional reinforcers for NR composites. Lastly, this work also reported the optimum Pb, Bi2O3, or Bi2S3 contents in NR and wood/NR composites at photon energies of 0.1, 0.5, 1, and 5 MeV, with 316–624 phr of filler being the recommended contents, of which the values depended on filler type and photon energy of interest. [ABSTRACT FROM AUTHOR]