Triggering Degradation of Cellulose Acetate by Embedded Enzymes: Accelerated Enzymatic Degradation and Biodegradation under Simulated Composting Conditions.

A green strategy that significantly accelerates the biodegradation rate of cellulose acetate (CA) by triggering deacetylation was demonstrated. Lipase isolated from Candida rugosa was immobilized on CA particles (immobilized lipase (IL)) by a physical entrapment method and further incorporated in CA films. After 40 days of aging in contact with external enzymes (lipase and cellulase), the number-average molecular weight (Mn) of CA/IL 5% decreased by 88%, while the Mn of CA only exhibited a 48% reduction. Fourier transform infrared and nuclear magnetic resonance spectroscopy of CA/IL 5% indicated significant deacetylation, which was further supported by the decrease of the water contact angle from 59 to 16°. These drastic changes were not observed for CA. Similar differences in the degradation rate were observed during aging under simulated composting conditions. After 180 days of simulated composting, traces of CA/IL 5% were barely observable, while large pieces of CA still remained. This could open the door to modified lignocellulose materials with retained biodegradability, also reducing the requirements for the degradation environment as the process is initiated from inside of the material.

Crystalline titanium-dioxide nanofinish impregnated on electrospun stereocomplex poly (lactic acid) as non-woven nanotextile with superhydrophilic, anti-shrinkage, dark dyeing and waste dye removal ability for sustainable application.

An environmentally friendly non-woven nanotextile has been prepared using enantiomeric pairs of poly (lactic acid) PLA by electrospinning technique. Solution blending of synthesized high molecular weight (⁓105 Da) poly (L-lactic acid) PLLA and poly (D-lactic acid), PDLA for prolonged time stirring produce solely stereocrystallites (sc). The high crosslinking effect of sc-PLA has played an important role, with multifunctional behaviour on the addition of anatase-TiO2 (a-TiO2) in three different ways (Case-I-III). The high crystallinity of a-TiO2 (~7.14 nm), has been confirmed from XRD and TEM studies as 98 %. The nanofinish as studied in (Case -III) by dipping and drying has decreased the water contact angle for the electrospun sc-PLA nanotextile from highly hydrophobic (132°) to superhydrophilicity after 8 min. An easy demonstration of high temperature treated nanofabric (at 100 °C) has proven to obtain an anti-shrinkage sc-PLA nanofabric. Even, the presence of a-TiO2 has improved the colour strength ability of sc-PLA as a dark dyed nanofabric. The loading of as-synthesized a-TiO2 nanoparticle has enhanced adsorbent dosages for 5TdipscPLA up to 1.44 mg/g of MB dosage, at contact time (8 h), and 68 % methylene blue (MB) removal efficiency under UV irradiation. Thereby, this a-TiO2 impregnated sc-PLA nanofabric tends to dye removal.

Functionalized poly(lactic acid) based nano-fabric for anti-viral applications.

This study endeavoured to explore and fabricate antiviral and antibacterial facemasks using zinc (oligo-lactate) (ZL), developed through a microwave synthesis technique. The prepared nano-fabric layer has excellent antiviral and antibacterial properties against Newcastle Disease Virus (NDV) and E. coli and S. aureus, respectively. Thermogravimetric analysis (TGA) of ZL shows a two-step thermal degradation, which confirms the formation of low molecular weight end group lactyl units with zinc ions. Another investigation using varying ZL concentration and silk nanocrystal (SNC) with poly(lactic acid) (PLA) and electrospinning them into nanofibres led to the fabrication of a facile and sustainable nanofabric that can be utilized as a protective layer for facemasks. Morphological analysis revealed the successful preparation of the nanofabric with proper distribution and uniformity in fibre diameter. Hydrophobicity of the prepared nanofabric confirmed excellent protection from water droplets that may transpire during coughing or sneezing by an infected individual. Breathability and reusability tests confirmed that the prepared facemask could be reused by ethanol washing without compromising its surface properties till 4 cycles. The PLA/ZL nanofabric layer demonstrated 97% antiviral efficacy against NDV in 10 minutes. In conclusion, the electrospun nanofabric layer can be used as a facemask having high hydrophobicity, good breathability, antibacterial, and antiviral properties to control the spread of contagious diseases.

Biodegradable kinetics and behavior of bio-based polyblends under simulated aerobic composting conditions.

The current study evaluates aerobic biodegradation of melt extruded poly(lactic acid) PLA based blends under composting conditions. Samples of neat PLA (NPLA) and bio-based polyblend composites of PLA/LLDPE (linear low-density polyethylene) having different concentration of MCC (microcrystalline cellulose crystal) were analyzed to understand the biodegradation behavior of these blends under simulated composting conditions. Biodegradation kinetics revealed that higher content of MCC and PLA accelerated the biodegradation process of the polymeric blends. Increase in the spherulite growth size and decrease in the spherulite density of the biodegraded samples confirmed the decline in amorphous portion of the test samples due to microbial assimilation, leaving behind the crystalline portion. Surface morphological analysis revealed that the samples of PLA/LLDPE/MCC blends underwent surface erosion prior to bulk biodegradation (50-80%) until the 90th day and the PLA formed fibril-like structures after degradation. This study would help in the design and preparation of biodegradable bio-based commercial blends in the future.

End-of-life evaluation and biodegradation of Poly(lactic acid) (PLA)/Polycaprolactone (PCL)/Microcrystalline cellulose (MCC) polyblends under composting conditions.

The present study evaluates biodegradation of the polyblends of poly(lactic acid) (PLA), polycaprolactone (PCL) and microcrystalline cellulose (MCC) in different compositions and comparison of the properties of those blends with that of neat PLA and neat PCL. The samples were melt extruded and blended to evaluate the environmental fate of the polyblends under simulated composting conditions following the standard ASTM International D5338-15 protocol. It was seen that blends with a higher concentration of PCL and MCC in the PLA matrix showed higher carbon mineralization percentage in comparison to the blends having low PCL and MCC components. Molecular weight analysis of the samples showed a decrease in their weight due to chain scission mechanism leading to the formation of intermediates. Analytical techniques revealed the formation of microbial biofilms on the blended biopolymeric surfaces. Field emission scanning electron microscopy showed the formation of fibril-like structures by PLA, and the formation of rough patches on the PCL surface re-confirmed biodegradation of the samples. This work fuels interest in the material characterization of PLA/PCL/MCC based polyblends and helps in tuning the biodegradability of the studied samples according to the demands.