scholarly journals Miscibility study of solution cast blends of poly(lactic acid) and poly(vinyl butyral)

2005 ◽  
Vol 23 (1) ◽  
pp. 22 ◽  
Author(s):  
J R Khurma ◽  
D R Rohindra ◽  
R Devi
Keyword(s):  
Lactic Acid ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
Casting Method ◽  
Scanning Calorimetry ◽  
Appreciable Change ◽  
Solution Cast ◽  
Solution Casting Method ◽  
The Common ◽  
Vinyl Butyral

Poly(lactic acid) (PLA) was blended with poly(viny1 butyral) (PVB) through solution casting method using chloroform as the common solvent. The films obtained were characterized for miscibility using Differential Scanning Calorimetry (DSC), tensile testing and FTIR spectroscopy. The DSC results showed that the glass-transition temperature (Tg) of the PLA and PVB remained more or less constant with the composition of the blend. The existence of two Tg?s in the blends indicated that PLA and PVB were immiscible over the composition range investigated. percentage crystallinity ( cc ), of PLA phase remained constant with increasing PVB content in the blend. FTIR measurements showed that there was no appreciable change in the spectra with respect to blend composition, implying the immiscibility of the two polymers. Mechanical analysis showed that the tensile strength and elongation decreased on blending.

scholarly journals Bio-composites for Fused Filament Fabrication. Effects of Maleic Anhydride Grafting on Poly(Lactic Acid) and Microcellulose

2021 ◽  
Author(s):  
Daniele Rigotti ◽  
Luca Fambri ◽  
Alessandro Pegoretti
Keyword(s):  
Lactic Acid ◽  
Maleic Anhydride ◽  
Nucleating Agent ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
Crystalline Cellulose ◽  
Fused Filament Fabrication ◽  
Scanning Calorimetry ◽  
Electron Microscopy Analysis ◽  
Reactive Mixing

Abstract Composite filaments consisting of poly(lactic acid) (PLA) and micro crystalline cellulose (MCC) were successfully used for additive manufacturing (AM) by fused filament fabrication (FFF). PLA and MCC bio-composites were obtained by direct mixing in a melt compounder; maleic anhydride (MAH) was also grafted onto PLA in reactive mixing stage to evaluate its effect on the final properties of the printed material. Filaments with various concentrations of MCC (up to a maximum content of 10 wt%) were produced with a single screw extruder and used to feed a commercial desktop FFF printer. Upon grafting of PLA with MAH, a more coherent interfacial morphology between PLA and MCC was detected by electron microscopy analysis. The thermal degradation of the PLA was unaffected by the presence of MCC and MAH. According to differential scanning calorimetry and dynamic mechanical analysis results, micro-cellulose acted as nucleating agent for PLA. In fact, the crystallization peak shifted towards lowers temperature and a synergistic effect when MCC was added to PLA grafted with MAH was observed possibly due to the increase of the chain mobility. Micro cellulose led to an increase in the stiffness of the material in both filaments and 3D printed specimen, however, a different fracture behavior was observed due to the peculiar structure of printed samples.

scholarly journals Influence of the Lignin Content on the Properties of Poly(Lactic Acid)/lignin-Containing Cellulose Nanofibrils Composite Films

Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1013 ◽  
Author(s):  
Xuan Wang ◽  
Yuan Jia ◽  
Zhen Liu ◽  
Jiaojiao Miao
Keyword(s):  
Lactic Acid ◽  
Lignin Content ◽  
Cellulose Nanofibrils ◽  
Composite Films ◽  
Tensile Tests ◽  
Nucleating Agent ◽  
Mechanical Analysis ◽  
Degree Of Crystallinity ◽  
Poly Lactic Acid ◽  
Scanning Calorimetry

Poly(lactic acid) (PLA)/lignin-containing cellulose nanofibrils (L-CNFs) composite films with different lignin contents were produced bythe solution casting method. The effect of the lignin content on the mechanical, thermal, and crystallinity properties, and PLA/LCNFs interfacial adhesion wereinvestigated by tensile tests, thermogravimetric analysis, differential scanning calorimetry (DSC), dynamic mechanical analysis, Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The tensile strength and modulus of the PLA/9-LCNFs (9 wt % lignin LCNFs) composites are 37% and 61% higher than those of pure PLA, respectively. The glass transition temperature (Tg) decreases from 61.2 for pure PLA to 52.6 °C for the PLA/14-LCNFs (14 wt % lignin LCNFs) composite, and the composites have higher thermal stability below 380 °C than pure PLA. The DSC results indicate that the LCNFs, containing different lignin contents, act as a nucleating agent to increase the degree of crystallinity of PLA. The effect of the LCNFs lignin content on the PLA/LCNFs compatibility/adhesion was confirmed by the FTIR, SEM, and Tg results. Increasing the LCNFs lignin content increases the storage modulus of the PLA/LCNFs composites to a maximum for the PLA/9-LCNFs composite. This study shows that the lignin content has a considerable effect on the strength and flexibility of PLA/LCNFs composites.

Structure and properties of poly(lactic acid)/poly(lactic acid)-α-cyclodextrin inclusion compound composites

2017 ◽  
Vol 37 (9) ◽  
pp. 897-909
Author(s):  
Li Zhang ◽  
Weijun Zhen ◽  
Yufang Zhou
Keyword(s):  
Lactic Acid ◽  
Average Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
Polymerization Temperature ◽  
Scanning Calorimetry ◽  
Synthesis Conditions ◽  
Cyclodextrin Inclusion ◽  
Comprehensive Performance

Abstract Poly(lactic acid) (PLA) was synthesized using a green catalyst, nano-zinc oxide (ZnO). The optimum synthesis conditions of PLA were as follows: a stoichiometric amount of 0.5 wt% of nano-ZnO, polymerization time of 14 h, and polymerization temperature of 170°C. Gel permeation chromatography results showed that the weight-average molecular weight (Mw) of PLA was 13,072 g/mol with a polydispersity index (PDI) of 1.7. Furthermore, PLA-α-cyclodextrin inclusion compounds (PLA-CD-ICs) were prepared by ultrasonic co-precipitation techniques. X-ray diffraction analysis and Fourier transform infrared spectroscopy demonstrated the change in lattice of α-CD from a cage configuration to a tunnel structure and the existence of some physical interactions between α-CD and PLA in the PLA-CD-ICs. To enhance the crystallization properties of PLA, PLA/PLA-CD-IC composites were blended with different contents of PLA-CD-ICs as nucleating agents. The crystallization behavior and comprehensive performance were investigated by differential scanning calorimetry, polarized optical microscopy, tensile testing, dynamic mechanical analysis, and scanning electron microscopy. Compared to PLA, the crystallinities of PLA/PLA-CD-IC composites were increased by 24.0%, 26.3%, 27.3%, and 31.8%. The results of all the analyses proved that PLA-CD-ICs were useful as green organic nucleators and improved the comprehensive performance of PLA materials.

Poly(lactic acid) phase transitions in the presence of nano calcium carbonate: Opposing effect of nanofiller on static and dynamic measurements

2018 ◽  
Vol 32 (3) ◽  
pp. 312-327 ◽  
Author(s):  
Omid Yousefzade ◽  
Javad Jeddi ◽  
Elham Vazirinasab ◽  
Hamid Garmabi
Keyword(s):  
Lactic Acid ◽  
Glass Transition ◽  
Calcium Carbonate ◽  
Mechanical Analysis ◽  
Polymer Chains ◽  
Poly Lactic Acid ◽  
Modulated Dsc ◽  
Scanning Calorimetry ◽  
Chain Mobility ◽  
Dispersion State

The effect of stearic acid-coated nano calcium carbonate (NCC) on transitions and chain mobility of poly(lactic acid) (PLA) was investigated. Dispersion state of NCC in polymeric matrix was explored using scanning electron microscopy and surface tension component measurements. Trends of PLA transitional phenomena were investigated using the results of dynamical mechanical analysis (DMA) and differential scanning calorimetry (DSC) in the nanocomposite systems based on PLA and NCC. In addition, two types of crystal structures and decreasing the glass transition temperature were distinguished using temperature-modulated DSC (TMDSC). Higher melting points of polymer crystals were found in TMDSC experiments due to low and dynamic heating rate compared to the conventional DSC. Dynamics of polymer chains, affected by NCC, were quantified using cooperativity length, ξ α, and the number of relaxing structural units, Nα, in the glass transition region. NCC particles hindered the cooperative motion of polymer chains at glass transitions and crystallization in TMDSC measurements, whereas the DMA results indicated that NCC particles may act as lubricant and simplified chain mobility.

Plasticizing effects of citrate esters on properties of poly(lactic acid)

2016 ◽  
Vol 36 (4) ◽  
pp. 371-380 ◽  
Author(s):  
Mounira Maiza ◽  
Mohamed Tahar Benaniba ◽  
Valérie Massardier-Nageotte
Keyword(s):  
Differential Scanning Calorimetry ◽  
Lactic Acid ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Intermolecular Hydrogen Bonds ◽  
X Ray ◽  
Triethyl Citrate ◽  
Acetyl Tributyl Citrate

Abstract Triethyl citrate (TEC) and acetyl tributyl citrate (ATBC) were used as plasticizer for poly(lactic acid) (PLA). The treated and plasticized PLA at various concentrations were analyzed by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and opacity. DSC was used to evaluate the crystallinity and thermal property of all the samples. It was found that the glass transition temperature (Tg) and the melting temperature (Tm) decreased as the amount of citrate esters increased. Additionally, the presence of TEC or ATBC tended to increase the crystallinity of PLA. This result was supported by XRD. DMA of plasticized PLA indicates that a decrease in Tg is obtained with increasing plasticizer content. FTIR spectra indicate that there are some molecular interactions by intermolecular hydrogen bonds between PLA and citrate esters. The effect of the concentration of plasticizer on the opacity of the films was negligible.

scholarly journals Poly(ε-Caprolactone)/Poly(Lactic Acid) Blends Compatibilized by Peroxide Initiators: Comparison of Two Strategies

Polymers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 228 ◽  
Author(s):  
Marta Przybysz-Romatowska ◽  
Józef Haponiuk ◽  
Krzysztof Formela
Keyword(s):  
Lactic Acid ◽  
Melt Flow Index ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
Flow Index ◽  
Infrared Spectrometry ◽  
Thermal And Mechanical Properties ◽  
Reactive Blending ◽  
Scanning Calorimetry ◽  
Reaction In Solution

Poly(ε-caprolactone) (PCL) and poly(lactic acid) (PLA) blends were compatibilized by reactive blending and by copolymers formed during reaction in the solution. The reactive blending of PCL/PLA was performed using di-(2-tert-butyl-peroxyisopropyl)benzene (BIB) or dicumyl peroxide (DCP) as radical initiator. PCL-g-PLA copolymers were prepared using 1.0 wt. % of DCP or BIB via reaction in solution, which was investigated through a Fourier transform infrared spectrometry (FTIR) and nuclear magnetic resonance (NMR) in order to better understand the occurring mechanisms. The effect of different additions such as PCL-g-PLA copolymers, DCP, or BIB on the properties of PCL/PLA blends was studied. The unmodified PCL/PLA blends showed a sea-island morphology typical of incompatible blends, where PLA droplets were dispersed in the PCL matrix. Application of organic peroxides improved miscibility between PCL and PLA phases. A similar effect was observed for PCL/PLA blend compatibilized by PCL-g-PLA copolymer, where BIB was used as initiator. However, in case of application of the peroxides, the PCL/PLA blends were cross-linked, and it has been confirmed by the gel fraction and melt flow index measurements. The thermal and mechanical properties of the blends were also investigated by means of differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), and tensile strength.

Structural Changes in Poly(lactic acid)/Hydroxyapatite Nanocomposites by Gamma Irradiation

2013 ◽  
Vol 829 ◽  
pp. 258-262
Author(s):  
Susan Dadbin ◽  
Faranak Naimian ◽  
Sorour Hasanpoor
Keyword(s):  
Lactic Acid ◽  
Gamma Irradiation ◽  
Irradiation Dose ◽  
Structural Changes ◽  
Chain Scission ◽  
Poly Lactic Acid ◽  
Casting Method ◽  
Radiation Induced ◽  
Solution Casting Method ◽  
Crosslinking Reactions

Poly (lactic acid)/hydroxyapatite (PLA/HAP) nanocomposites were made via solution casting method and subjected to gamma irradiation at doses of 30 and 50 kGy. FTIR spectra of the nanocomposites displayed structural changes in the crystalline phase of PLA upon irradiation. The PLA/HAP nanocomposites of 6 and 10 pph HAP irradiated at 30 kGy showed higher tensile strengths. This was attributed to radiation-induced crystallinity that verified by DSC crystallinity measurements. Using triallyl isocyanurate (TAIC) as a multifunctional monomer promoted radiation-induced crosslinking reactions in PLA that was manifested by improvements in the tensile strength of the nanocomposites. Optimum values for TAIC, irradiation dose and HAP content were found as 1 pph, 30 kGy and 10 pph respectively. Raising the irradiation dose from 30 to 50 kGy prompted chain scission reactions that had adverse effects on tensile properties.

Effect of Polyethylene Glycol in Nanocellulose/PLA Composites

2019 ◽  
Vol 821 ◽  
pp. 89-95
Author(s):  
Wanasorn Somphol ◽  
Thipjak Na Lampang ◽  
Paweena Prapainainar ◽  
Pongdhorn Sae-Oui ◽  
Surapich Loykulnant ◽  
...  
Keyword(s):  
Tensile Strength ◽  
Lactic Acid ◽  
Polyethylene Glycol ◽  
Aspect Ratio ◽  
Mechanical Performance ◽  
Tensile Modulus ◽  
Poly Lactic Acid ◽  
Solvent Casting ◽  
Casting Method ◽  
Mediated Oxidation

Poly (lactic acid) or PLA was reinforced by nanocellulose and polyethylene glycol (PEG), which were introduced into PLA matrix from 0 to 3 wt.% to enhance compatibility and strength of the PLA. The nanocellulose was prepared by TEMPO-mediated oxidation from microcrystalline cellulose (MCC) powder and characterized by TEM, AFM, and XRD to reveal rod-like shaped nanocellulose with nanosized dimensions, high aspect ratio and high crystallinity. Films of nanocellulose/PEG/PLA nanocomposites were prepared by solvent casting method to evaluate the mechanical performance. It was found that the addition of PEG in nanocellulose-containing PLA films resulted in an increase in tensile modulus with only 1 wt% of PEG, where higher PEG concentrations negatively impacted the tensile strength. Furthermore, the tensile strength and modulus of nanocellulose/PEG/PLA nanocomposites were higher than the PLA/PEG composites due to the existence of nanocellulose chains. Visual traces of crazing were detailed to describe the deformation mechanism.

scholarly journals Relationship between the Stereocomplex Crystallization Behavior and Mechanical Properties of PLLA/PDLA Blends

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1851
Author(s):  
Hye-Seon Park ◽  
Chang-Kook Hong
Keyword(s):  
Mechanical Properties ◽  
Lactic Acid ◽  
Crystallization Behavior ◽  
Mechanical Analysis ◽  
X Ray Diffraction ◽  
Nucleation Agent ◽  
Scanning Calorimetry ◽  
Nucleation Sites ◽  
Wide Range ◽  
Degree Of Crystallization

Poly (l-lactic acid) (PLLA) is a promising biomedical polymer material with a wide range of applications. The diverse enantiomeric forms of PLLA provide great opportunities for thermal and mechanical enhancement through stereocomplex formation. The addition of poly (d-lactic acid) (PDLA) as a nucleation agent and the formation of stereocomplex crystallization (SC) have been proven to be an effective method to improve the crystallization and mechanical properties of the PLLA. In this study, PLLA was blended with different amounts of PDLA through a melt blending process and their properties were calculated. The effect of the PDLA on the crystallization behavior, thermal, and mechanical properties of PLLA were investigated systematically by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray diffraction (XRD), polarized optical microscopy (POM), dynamic mechanical analysis (DMA), and tensile test. Based on our findings, SC formed easily when PDLA content was increased, and acts as nucleation sites. Both SC and homo crystals (HC) were observed in the PLLA/PDLA blends. As the content of PDLA increased, the degree of crystallization increased, and the mechanical strength also increased.

scholarly journals Study on Structure, Thermal Behavior, and Viscoelastic Properties of Nanodiamond-Reinforced Poly (vinyl alcohol) Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1426
Author(s):  
Tomáš Remiš ◽  
Petr Bělský ◽  
Tomáš Kovářík ◽  
Jaroslav Kadlec ◽  
Mina Ghafouri Azar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Mechanical Analysis ◽  
Single Step ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Primary Particles ◽  
Solution Casting Method ◽  
Average Size

In this work, advanced polymer nanocomposites comprising of polyvinyl alcohol (PVA) and nanodiamonds (NDs) were developed using a single-step solution-casting method. The properties of the prepared PVA/NDs nanocomposites were investigated using Raman spectroscopy, small- and wide-angle X-ray scattering (SAXS/WAXS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It was revealed that the tensile strength improved dramatically with increasing ND content in the PVA matrix, suggesting a strong interaction between the NDs and the PVA. SEM, TEM, and SAXS showed that NDs were present in the form of agglomerates with an average size of ~60 nm with primary particles of diameter ~5 nm. These results showed that NDs could act as a good nanofiller for PVA in terms of improving its stability and mechanical properties.

Sign in / Sign up

Export Citation Format

Share Document