Foram Dave

Ms. Foram Dave

Centre for Precision Engineering, Materials and Manufacturing (PEM) Centre, Institute of Technology Sligo, Ash Lane, Sligo, Ireland
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orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 February 2021 in Polymers
Verified
Journal Article
Open access
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KRKrzysztof Rodzeń
Krzysztof Rodzeń
Preetam SharmaPreetam Sharma
Preetam Sharma
Alistair T. McIlhaggerAlistair T. McIlhagger
Alistair T. McIlhagger
MMMozaffar Mokhtari
Mozaffar Mokhtari
Foram DaveForam Dave
Foram Dave
Adrian BoydAdrian Boyd
Adrian Boyd
The manufacture of polyetheretherketone/hydroxyapatite (PEEK/HA) composites is seen as a viable approach to help enhance direct bone apposition in orthopaedic implants. A range of methods have been used to produce composites, including Selective Laser Sintering and injection moulding. Such techniques have drawbacks and lack flexibility to manufacture complex, custom-designed implants. 3D printing gets around many of the restraints and provides new opportunities for innovative solutions that are structurally suited to meet the needs of the patient. This work reports the direct 3D printing of extruded PEEK/HA composite filaments via a Fused Filament Fabrication (FFF) approach. In this work samples are 3D printed by a custom modified commercial printer Ultimaker 2+ (UM2+). SEM-EDX and µCT analyses show that HA particles are evenly distributed throughout the bulk and across the surface of the native 3D printed samples, with XRD highlighting up to 50% crystallinity and crystalline domains clearly observed in SEM and HR-TEM analyses. This highlights the favourable temperature conditions during 3D printing. The yield stress and ultimate tensile strength obtained for all the samples are comparable to human femoral cortical bone. The results show how FFF 3D printing of PEEK/HA composites up to 30 wt% HA can be achieved.

24 February 2021 in Polymers
Verified
Journal Article
Open access
PDF file
Foram DaveForam Dave
Foram Dave
Muhammad Mahmood AliMuhammad Mahmood Ali
Muhammad Mahmood Ali
RSRichard Sherlock
Richard Sherlock
AKAsokan Kandasami
Asokan Kandasami
DTDavid Tormey
David Tormey
The present review provides an overview of the current status and future perspectives of one of the smart manufacturing techniques of Industry 4.0, laser transmission welding (LTW) of semi-crystalline (SC) polymers and their composites. It is one of the most versatile techniques used to join polymeric components with varying thickness and configuration using a laser source. This article focuses on various parameters and phenomena such as inter-diffusion and microstructural changes that occur due to the laser interaction with SC polymers (specifically polypropylene). The effect of carbon black (size, shape, structure, thermal conductivity, dispersion, distribution, etc.) in the laser absorptive part and nucleating agent in the laser transmissive part and its processing conditions impacting the weld strength is discussed in detail. Among the laser parameters, laser power, scanning speed and clamping pressure are considered to be the most critical. This review also highlights innovative ideas such as incorporating metal as an absorber in the laser absorptive part, hybrid carbon black, dual clamping device, and an increasing number of scans and patterns. Finally, there is presented an overview of the essential characterisation techniques that help to determine the weld quality. This review demonstrates that LTW has excellent potential in polymer joining applications and the challenges including the cost-effectiveness, innovative ideas to provide state-of-the-art design and fabrication of complex products in a wide range of applications. This work will be of keen interest to other researchers and practitioners who are involved in the welding of polymers.

28 April 2022 in Polymers
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Journal Article
Open access
PDF file
Hao WuHao Wu
Hao Wu
Foram DaveForam Dave
Foram Dave
MMMozaffar Mokhtari
Mozaffar Mokhtari
Muhammad Mahmood AliMuhammad Mahmood Ali
Muhammad Mahmood Ali
RSRichard Sherlock
Richard Sherlock
Shaun McFaddenShaun McFadden
Shaun McFadden
Hardness is a useful measure of a material’s resistance to permanent indentation; but for viscoelastic polymers, hardness data are highly dependent on the test type and the parameter set chosen. Vickers microhardness testing is used to leave small indents (<150 µm) and is shown to be applicable to polymers. A detailed investigation of the required steps for microhardness testing in isotactic polypropylene (iPP) is provided. Samples should be mounted in epoxy resin in order to maintain curing temperatures at room temperature. Mounted samples can be ground and polished in a semi-automatic polisher using graduated SiC paper (wet grinding) but progressing onto alumina suspension for polishing. Final polishing should be performed with 0.05-µm alumina suspension. The hardness measured was shown to be dependent on load and dwell time with a much greater dependency on dwell time. Strain recovery was shown to be completed after a time period equal to the dwell time. This study shows that indents can be measured thereafter, and it is recommended that they be measured within a 24 h period after the indent was created. After data fitting, the equation for hardness was shown to follow a power law with load and dwell time as the main variables. Fitting parameters were compared to those found in the literature, and it was found that parameters were significantly different to those reported elsewhere. Therefore, this study highlights the importance of calibrating on a case-by-case basis. Finally, to show the usefulness of the Vickers micro-hardness testing method, the calibrated test method was applied on iPP with additions of carbon black up to 3 wt.%. Comparisons were made with data from the literature, but the hardness data generated in our work were found to be at least twice that reported in the literature. The testing parameters were not cited in the literature: specifically, the dwell time was not provided, and this generated doubt on the usefulness of the cited data. Hence, this work is intended to serve as an exemplar of how to prepare and proceed with hardness testing of polymers.

1 January 2023 in AIP Conference Proceedings
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Conference Paper
Open access
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Foram DaveForam Dave
Foram Dave
JJJosemon Jacob
Josemon Jacob
AKAsokan Kandasami
Asokan Kandasami
MMMarion McAfee
Marion McAfee
DTDavid Tormey
David Tormey
Polylactide, PLA (also called Polylactic acid) is an aliphatic polyester that exhibits a slow rate of biodegradation due to its non-polar nature. In this study, it is demonstrated that gamma rays enhance the biodegradability of PLA. The pristine PLA samples were irradiated by gamma rays with various doses: i.e., 25, 50, 75, and 100 kGy. These irradiated samples were analyzed by the Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), derivative thermogravimetry (DTG), and contact angle measurements to understand the functionalization of this polymer. While the FTIR analysis shows the emergence of a new band at 3400-3600 cm-1 corresponding to -OH groups in alcohols, hydroperoxides, and carboxylic acids, the TGA results exhibit a change from a single step to a two-step degradation pathways upon γ-rays irradiation which is attributable to the formation of polar -OH groups. The DSC results indicate a decrease in Tg due to the decrease in the molecular weight after γ-rays irradiation which is also consistent with the results from the gel permeation chromatography. The decrease in the contact angles of the γ-rays irradiated samples provides evidence for hydroxyl functionalization. This study shows that γ-rays irradiation enhances the biodegradability of PLA.