Gisha Elizabeth Luckachan

Bio: Gisha Elizabeth Luckachan is an academic researcher from Council of Scientific and Industrial Research. The author has contributed to research in topics: Molecular sieve & Low-density polyethylene. The author has an hindex of 4, co-authored 4 publications receiving 584 citations.

Biodegradable Polymers- A Review on Recent Trends and Emerging Perspectives

Abstract: Recent trends in biodegradable polymers indicate significant developments in terms of novel design strategies and engineering to provide advanced polymers with comparably good performance. However, there are several inadequacies in terms of either technology or cost of production especially in the case of applications in environmental pollution. So, there is a need to have a fresh perspective on the design, properties and functions of these polymers with a view to developing strategies for future developments. The paper reviews the present state-of-art on biodegradable polymers and discusses the salient features of the design and properties of biodegradable polymers. Special emphasis is given to the problems and prospects of (1) approaches adopted to make non-biodegradable synthetic polymers such as polyethylene biodegradable and (2) biodegradable polymers and copolymers made from renewable resources especially poly(lactic acid) based polymers and copolymers which are emerging as the candidate biodegradable materials for the future.

Random multiblock poly(ester amide)s containing poly(L‐lactide) and cycloaliphatic amide segments: Synthesis and biodegradation studies

Abstract: Novel multiblock poly(ester amide)s containing poly(L-lactide) and cycloaliphatic amide segments were synthesized from telechelic oligomer of α,ω-hydroxyl terminated poly(L-lactide), 1,3-cyclohexylbis(methylamine), and sebacoylchloride by the “two-step” interfacial polycondensation method. The blocky nature of PEAs was established by FTIR and 1H NMR spectroscopies. The effect of relative content of ester and amide segments on the crystallization nature of PEAs was investigated by WAXD and DSC analyses. PEAs having lower content of PLLA, PEA 1 and PEA 2, showed a crystallization pattern analogous to polyamides, whereas PEA 3, having higher content of PLLA, showed two crystalline phases characterized by polyester and polyamide segments. Random nature of PEAs was observed from single Tg values. Biodegradation studies using the enzyme lipase from Candida Cylindracea showed higher degradation rate for PEA 3 than that for PEA 1 and PEA 2. FTIR, 1H NMR, and DSC analyses of the degraded products indicated the involvement of ester linkages in the degradation process. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3250–3260, 2006

Water Vapor Adsorption Capacity Loss of Molecular Sieves 4A, 5A, and 13X Resulting from Methanol and Heptane Exposure

Abstract: Zeolite-based molecular sieves are applied in industrial dehydration units for their high water uptake capacities and extremely low equilibrium pressure of water vapor. During their operational life, they tend to lose their water vapor adsorption capacity slowly. To optimize the usage of molecular sieves in dryer units, it is vital to understand the mechanism(s) leading to deactivation. In this work, the capacity loss was studied by exposing LTA- and FAU-type zeolites to methanol and heptane vapors under relatively harsh conditions using repetitive adsorption/regeneration cycles. A simple microflow unit was designed and used for the deactivation experiments. The water vapor adsorption capacity of the resulting samples was measured using a gravimetric analyzer. In addition, they were characterized by classic XRD, 13C NMR, and TGA techniques. The crystallinity of fresh and spent zeolite XRD patterns was not drastically affected even after exposure to the contaminants. It was found that methanol easily gave rise to a severe loss of water vapor adsorption capacity, much more so than heptane. Water vapor uptake in the methanol exposed samples is ∼50% lower than that for the fresh zeolites. This is attributed to nonvolatile, residual hydrocarbons.

Chitosan-modifications and applications: Opportunities galore

Abstract: Of late, the most bountiful natural biopolymer chitin and chitosan have become cynosure of all party because of an unusual combination of biological activities plus mechanical and physical properties. However applications of chitin are limited due to its inherent insoluble and intractable nature. Chitosan, alkaline hydrolytic derivative of chitin has better solubility profile, less crystallinity and is amenable to chemical modifications due to presence of functional groups as hydroxyl, acetamido, and amine. The chemical modification of chitosan is of interest because the modification would not change the fundamental skeleton of chitosan, would keep the original physicochemical and biochemical properties and finally would bring new or improved properties. In view of rapidly growing interest in chitosan its chemical aspects and chemical modification studies is reviewed. The several chemical modifications such as oligomerization, alkylation, acylation, quternization, hydroxyalkylation, carboxyalkylation, thiolation, sulfation, phosphorylation, enzymatic modifications and graft copolymerization along with many assorted modifications have been carried out. The chemical modification affords a wide range of derivatives with modified properties for specific end use applications in diversified areas mainly of pharmaceutical, biomedical and biotechnological fields. Assorted modifications including chitosan hybrids with sugars, cyclodextrin, dendrimers, and crown ethers have also emerged as interesting multifunctional macromolecules. The versatility in possible modifications and applications of chitosan derivatives presents a great challenge to scientific community and to industry. The successful acceptance of this challenge will change the role of chitosan from being a molecule in waiting to a lead player.