Jute fabrics-reinforced linear low density polyethylene (LLDPE) matrix composites (50 wt% fiber) were prepared by compression molding and mechanical properties were studied. Polyvinyl chloride (PVC) matrix was incorporated instead of LLDPE in the jute based composites and their mechanical properties were investigated and compared with the control composites. It was found that with the increase of PVC in the LLDPE based composites, the mechanical properties were found to improve significantly. Degradation tests of the composites for upto 24 weeks were performed in soil medium. Water uptake and Thermo-mechanical properties of the composites were also studied.

Jute fabrics (hessian cloth) reinforced polyvinyl chloride (PVC) based composites were prepared by compression molding. Jute content varied from 40-60 wt% in the composites. Four layers of jute fabrics were compression molded with five layers of PVC. It was found that the composite containing 40% jute fabrics showed the best performance. The values of tensile strength (TS), bending strength (BS), tensile modulus (TM), and bending modulus (BM) of the composite (40 wt% jute fabrics) were found to be 59.3 MPa, 62.6 MPa, 1.3 GPa, and 3.2 GPa, respectively. The values of TS and BS were improved to 77% and 46%, respectively, compared to the matrix material PVC. Scanning electron microscopic analysis was carried out to investigate the interfacial properties of the composites. Degradation tests of the composites (up to 6 months) were performed in soil medium and showed partial degradation nature.

Composites (50 wt% fiber) of jute fiber reinforced polyvinyl chloride (PVC) matrix and E-glass fiber reinforced PVC matrix were prepared by compression molding. Mechanical properties such as tensile strength (TS), tensile modulus (TM), bending strength (BS), bending modulus (BM) and impact strength (IS) of both types of composites was evaluated and compared. Values of TS, TM, BS, BM and IS of jute fiber/PVC composites were found to be 45 MPa, 802 MPa, 46 MPa, 850 MPa and 24 kJ/m 2 , respectively. It was observed that TS, TM, BS, BM and IS of E-glass fiber/PVC composites were found to increase by 44, 80, 47, 92 and 37.5%, respectively. Thermal properties of the composites were also carried out, which revealed that thermal stability of E-glass fiber/PVC system was higher. The interfacial adhesion between the fibers (jute and E-glass) and matrix was studied by means of critical fiber length and interfacial shear strength that were measured by single fiber fragmentation test. Fracture sides after flexural testing of both types of the composites were investigated by Scanning Electron Microscopy.

Jute fabrics such as reinforced polyvinyl chloride (PVC), polypropylene (PP), and a mixture of PVC and PP matrices-based composites (50 wt% fiber) were prepared by compression molding. Tensile strength (TS), bending strength (BS), tensile modulus (TM), and vbending modulus (BM) of jute fabrics' reinforced PVC composite (50 wt% fiber) were found to be 45 MPa, 52 MPa, 0.8 GPa, and 1.1 GPa, respectively. The effect of incorporation of PP on the mechanical properties of jute fabrics' reinforced PVC composites was studied. It was found that the mixture of 60% PP and 40% PVC matrices based composite showed the best performance. TS, BS, TM, and BM for this composite were found to be 65 MPa, 70 MPa, 1.42 GPa, and 1.8 GPa, respectively. Degradation tests of the composites for up to six months were performed in a soil medium. Thermo-mechanical properties of the composites were also studied.

Although FDA approved and clinically utilised, research on 45S5 Bioglass® and S53P4 including other bioactive glasses continues in order to advance their applicability for a range of alternate applications. For example, rendering these particles porous would enable incorporation of varying biological payloads (i.e. cells, drugs and growth factors) and making them spherical would enhance their flow properties enabling delivery to target sites via minimally invasive injection procedures. This paper reports on the manufacture of solid (non-porous; SGMS) and highly porous microspheres (PGMS) with large external pores and fully interconnected porosity from bioactive silicate glass formulations (45S5 and S53P4) via a single stage flame spheroidisation process and their physicochemical properties including in vitro biological response. Morphological and physical characterisation of the SGMS and PGMS revealed interconnected porosity up to 65 ± 5%. Mass loss studies comparing between SGMS and PGMS revealed 1.5 times higher mass loss for the PGMS over 28 days. Also, in vitro bioactivity studies using simulated body fluid (SBF) revealed hydroxyapatite (HA) formation at earlier time point for PGMS compared to their SGMS counterparts (i.e day 1 for PGMS and day 3 for SGMS of 45S5). In addition, HA layers were also formed in cell culture media, with the exception of SGMS of 45S5, which revealed CaP formation with a ratio of 1.52–1.78. Direct cell seeding and indirect cell culture studies (via incubation with microsphere degradation products) revealed mouse 3T3 cells were able to grow and undergo osteogenic differentiation in vitro, confirming cytocompatibility of both 45S5 and S53P4 SGMS and PGMS. More importantly and especially for orthobiologic applications, cells were observed to have migrated within the pores of the PGMS. As such, the PGMS developed from these bioactive silicate glasses are highly promising candidate materials for orthobiologics and alternate applications requiring delivery of biologic payloads.