scholarly journals Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability

2018 ◽  
Vol 5 (3) ◽  
pp. 171686 ◽  
Author(s):  
Xiaoxiao Zhang ◽  
Tingyuan Gong ◽  
Hong Chi ◽  
Tianduo Li
Keyword(s):  
Self Assembly ◽  
Thermo Gravimetric Analysis ◽  
Size Control ◽  
Gel Permeation Chromatography ◽  
Decomposition Temperature ◽  
Inorganic Materials ◽  
Quantum Yields ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Perylene Bisimide

Size control has been successfully achieved in inorganic materials, but it remains a challenge in polymer nanomaterials due to their polydispersity. Here, we report a facile approach to tailor the diameters of polyurethane (PU) nanoparticles (490 nm, 820 nm and 2.1 µm) via perylene bisimide (PBI) assisted self-assembly. The formed morphologies such as spindle, spherical and core–shell structures depend on the ratio of PBI and polymer concentrations. It is shown that the formation of PU nanoparticles is directed by π–π stacking of PBI and the morphology transition is not only affected by the amount of PBI incorporated, but also influenced by solvent, which controls the initial evaporation balance. Furthermore, the prepared PUs exhibit retained optical stability and enhanced thermal stability. The PUs, designed to have conjugated PBI segments in backbones, were synthesized via ring-opening and condensation reactions. Compared with the neat PU, gel permeation chromatography shows narrower molecular weight distribution. Fluorescence spectra and ultraviolet–visible spectra indicate retained maximum emission wavelength of PBI at 574 nm and 5.2% quantum yields. Thermo-gravimetric analysis and differential scanning calorimetry reveal 79°C higher decomposition temperature and 22°C higher glass transition temperature. This study provides a new way to fabricate well-defined nanostructures of functionalized PUs.

scholarly journals Biocomposites of Bio-Polyethylene Reinforced with a Hydrothermal-Alkaline Sugarcane Bagasse Pulp and Coupled with a Bio-Based Compatibilizer

Molecules ◽  
2020 ◽  
Vol 25 (9) ◽  
pp. 2158
Author(s):  
Nanci Vanesa Ehman ◽  
Diana Ita-Nagy ◽  
Fernando Esteban Felissia ◽  
María Evangelina Vallejos ◽  
Isabel Quispe ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
3D Printing ◽  
Water Absorption ◽  
Sugarcane Bagasse ◽  
Thermo Gravimetric Analysis ◽  
Decomposition Temperature ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Cradle To Gate ◽  
Bagasse Pulp

Bio-polyethylene (BioPE, derived from sugarcane), sugarcane bagasse pulp, and two compatibilizers (fossil and bio-based), were used to manufacture biocomposite filaments for 3D printing. Biocomposite filaments were manufactured and characterized in detail, including measurement of water absorption, mechanical properties, thermal stability and decomposition temperature (thermo-gravimetric analysis (TGA)). Differential scanning calorimetry (DSC) was performed to measure the glass transition temperature (Tg). Scanning electron microscopy (SEM) was applied to assess the fracture area of the filaments after mechanical testing. Increases of up to 10% in water absorption were measured for the samples with 40 wt% fibers and the fossil compatibilizer. The mechanical properties were improved by increasing the fraction of bagasse fibers from 0% to 20% and 40%. The suitability of the biocomposite filaments was tested for 3D printing, and some shapes were printed as demonstrators. Importantly, in a cradle-to-gate life cycle analysis of the biocomposites, we demonstrated that replacing fossil compatibilizer with a bio-based compatibilizer contributes to a reduction in CO2-eq emissions, and an increase in CO2 capture, achieving a CO2-eq storage of 2.12 kg CO2 eq/kg for the biocomposite containing 40% bagasse fibers and 6% bio-based compatibilizer.

Synthesis, characterization and corrosion protection properties of polyN-(p-bromophenyl)-2-methacrylamide-co-glycidyl methacrylate on low nickel stainless steel

2011 ◽  
Vol 31 (2-3) ◽  
Author(s):  
Sakvai Mohammed Safiullah ◽  
Deivasigamani Thirumoolan ◽  
Kottur Anver Basha ◽  
K. Mani Govindaraju ◽  
Dhanraj Gopi ◽  
...  
Keyword(s):  
Stainless Steel ◽  
Corrosion Protection ◽  
Glycidyl Methacrylate ◽  
Electrochemical Impedance ◽  
Thermo Gravimetric Analysis ◽  
Gel Permeation Chromatography ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Protection Efficiency ◽  
Ft Ir

Abstract The synthesis of copolymers from different feed ratios of N-(p-bromophenyl)-2- methacrylamide (PBPMA) and glycidyl methacrylate (GMA) was achieved by using free radical solution polymerization technique and characterized using FT-IR, 1H and 13C NMR spectroscopy. The thermal stability of the synthesized copolymers was studied using thermo-gravimetric analysis (TGA) and differential scanning calorimetry (DSC). The molecular weight of the copolymer is determined by gel permeation chromatography (GPC). The corrosion performances of low nickel stainless steel specimens dip coated with different composition of copolymers were investigated in 0.5 M H2SO4 using potentiodynamic polarization and electrochemical impedance spectroscopic (EIS) techniques. The polarization and impedance measurements showed different corrosion protection efficiency with change in composition of the copolymers. It was found that the corrosion protection properties are owing to the barrier effect of the polymer layer covered on the low nickel stainless steel surfaces. However, it is observed that the mole ratio of PBPMA and GMA plays a major role in the protective nature of the copolymer.

Synthesis, Characterization and Isothermal Crystallization Kinetics of Poly(Dodecamethylene Terephthalamide)

2011 ◽  
Vol 284-286 ◽  
pp. 1894-1900
Author(s):  
Kai Feng Li ◽  
Peng Fu ◽  
Chuan Lin Liu ◽  
Qing Xiang Zhao ◽  
Min Ying Liu
Keyword(s):  
Crystallization Kinetics ◽  
Isothermal Crystallization ◽  
Thermo Gravimetric Analysis ◽  
Aromatic Polyamide ◽  
Decomposition Temperature ◽  
Proton Nuclear Magnetic Resonance ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Isothermal Crystallization Kinetics ◽  
Kinetics Of

A kind of semi-aromatic polyamide, poly(dodecamethylene terephthalamide) (PA12T) was synthesized via a three-step reaction of terephthalic acid and 1,12-dodecanediamine. The structure of the prepared PA12T was characterized by Fourier transform infrared (FT-IR) spectroscopy and proton nuclear magnetic resonance (1H-NMR). The thermal behaviour of PA12T was determined by differential scanning calorimetry (DSC), thermo-gravimetric analysis (TGA) and dynamic mechanical analysis (DMA). Melting temperature (Tm), glass transition temperature (Tg) and decomposition temperature (Td) of PA12T are 311°C, 144°C and 429°C, respectively. Isothermal crystallization kinetics of PA12T have been investigated in the temperature range of 270-280°C using DSC. The activation energies (ΔE) were determined to be -170.4 kJ/mol for the isothermal crystallization processes by the Arrhenius’ methods.

Processing and MWNT Composition Effects on the Thermal, Electrical and Mechanical Properties of PLA-MWNT Composites

2009 ◽  
Author(s):  
Reza R. Rizvi ◽  
Jae K. Kim ◽  
Hani E. Naguib
Keyword(s):  
Mechanical Properties ◽  
Thermo Gravimetric Analysis ◽  
Composite Films ◽  
Thermal Characteristics ◽  
Casting Process ◽  
Decomposition Temperature ◽  
Multiwall Carbon Nanotube ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Electrical Percolation

This paper investigates the processing and its effects and the effect of multiwall carbon nanotube (MWNT) composition on the thermal, electrical and mechanical properties of polylactide (PLA)-MWNT composites. The composite films were prepared by a solvent casting process using two solvents, chloroform and 1,4-dioxane. The dispersion of the MWNTs in PLA was examined using a scanning electron microscope and was found to be more improved when 1,4-dioxane was used as the solvent as compared to chloroform. The thermal characteristics of the composites were examined on Differential Scanning Calorimetry and Thermo-gravimetric Analysis. Composites prepared using 1,4-dioxane had greater improvements in composite decomposition temperature, glass transition temperature and displayed faster crystallization kinetics. The mechanical properties of the composites were tested in uniaxial tension. Composites prepared using chloroform had a lower modulus than composites prepared using 1,4-dioxane. The electrical AC conductivity of the composites was measured over a broad frequency spectrum. Composites prepared using 1,4-dioxane displayed electrical percolation at 0.5 wt.% MWNT in PLA while percolation was absent in 0.5 wt.% MWNT composites prepared using chloroform.

Self-Assembly of Methacrylic Nanostructured Copolymers Containing Polyhedral Oligomeric Silsesquioxanes

e-Polymers ◽  
2007 ◽  
Vol 7 (1) ◽  
Author(s):  
D. Molina ◽  
M. Levi ◽  
S. Turri ◽  
M. Penso
Keyword(s):  
Thermo Gravimetric Analysis ◽  
Gel Permeation Chromatography ◽  
Butyl Methacrylate ◽  
Random Copolymers ◽  
Gravimetric Analysis ◽  
X Rays ◽  
Polyhedral Oligomeric Silsesquioxanes ◽  
Scanning Calorimetry ◽  
Free Radical Copolymerization ◽  
Hybrid Copolymer

AbstractTwo hybrid copolymer series obtained by free-radical copolymerization of methacrylcyclohexyl Polyhedral oligomeric silsesquioxane (POSS) with butyl methacrylate or 2-ethylhexylmethacrylate were characterized by 1H-NMR spectroscopy, gel permeation chromatography (GPC), X-rays Diffraction (XRD), differential scanning calorimetry (DSC) and thermo-gravimetric analysis (TGA). Reactivity ratios were calculated by low yield composition data suggesting the formation of random copolymers with low probability of poly-POSS sequences. XRD studies showed the crystallization behaviour of the inorganic phase independently on the POSS content; however sample processing by solvent casting effectively hindered the copolymer self-assembling ability. DSC suggests the formation of polyphasic structures with Tg increasing with POSS content, and with endothermal peaks occurring at higher temperature. Finally TGA shows an improved thermal stability of hybrid copolymers with char yield correlated to the level of inorganic phase.

Reach on P/N Type Intumescent Flame Retardant for Polyester Fabric

2013 ◽  
Vol 785-786 ◽  
pp. 714-717 ◽  
Author(s):  
Yi Zhou ◽  
Yong Zhu Cui ◽  
Guo Jun Liu ◽  
Li Hua Lv
Keyword(s):  
Flame Retardant ◽  
Flame Retardants ◽  
Thermo Gravimetric Analysis ◽  
Polyester Fabric ◽  
Decomposition Temperature ◽  
Intumescent Flame Retardant ◽  
Curing Temperature ◽  
Optimum Process ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry

An intumescent flame retardant (IFR) containing phosphorus and APP was applied to polyester fabric. The finishing process was optimized and the properties of treated fabric were characterized. The optimum process was as follows: the total dosage of IFR system was 40%, the mass ratio of phosphorus-containing flame retardants and APP was 7:3, and curing temperature was 180°C. The treated PET fabrics imparted good resistance to melt drop. Characterization of the thermo-gravimetric analysis, differential scanning calorimetry (DSC) indicated that much more residual char with intumescent structure, the incombustible gas and water were formed during combustion of flame retardant polyester fabric, whose decomposition temperature was lower compared to that of the untreated sample.

Graphene Nanoplates Filled Nylon 6,6 Nanocomposites, Morphological, Thermal, Mechanical and Solvent Uptake Study

2019 ◽  
Vol 41 (3) ◽  
pp. 388-388
Author(s):  
Khalid Saeed Khalid Saeed ◽  
Tariq Shah and Ahmad Hassan Tariq Shah and Ahmad Hassan
Keyword(s):  
Thermo Gravimetric Analysis ◽  
Neutral Red ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Nucleation Effect ◽  
Morphological Studies ◽  
Solvent Uptake ◽  
Nylon 6,6 ◽  
Dsc Analyses ◽  
Graphene Nanoplates

Effect of graphene nanoplates (GNPs) on the properties of Nylon 6,6 (Nyl 6,6) is investigated in present study. The morphological studies presented that the GNPs were dispersed inside the Nyl 6,6 matrix. The thermo gravimetric analysis (TGA) illustrated that the thermal degradation of nanocomposites samples were started at the range of 350-393 oC, which was appreciably higher than neat Nyl 6,6 (360 oC). The differential scanning calorimetry (DSC) analyses revealed that the crystallization temperature (Tc) of GNPs/Nyl 6,6 increased as increased the addition of GNPs, which might be due to the nucleation effect of GNPs. The mechanical properties of Nyl 6,6 was enhanced by incorporation of GNPs upto the addition of an optimal quantity of filler (5%wt GNPs) into the polymer matrix. The stress yield and Young’s modulus of 5%wt GNPs/Nyl 6,6 was 96.79 and 1.54, N/nm2, respectively. Both Nyl 6,6 and nanocomposites samples were also used for the adsorption of Neutral red chloride (NRC) dye, which significantly remove the dye from the aqueous solution. The neat nylon 6,6 and GNPs (5 and 10 wt%)/Nyl 6,6 adsorbed about 88.49, 93.15, and 93.60% within 2 h, respectively.

Characterization of Novel Solid Dispersions of Moringa oleifera Leaf Powder Using Thermo-Analytical Techniques

Processes ◽  
2021 ◽  
Vol 9 (12) ◽  
pp. 2230
Author(s):  
Nontsikelelo Noxolo Tafu ◽  
Victoria A. Jideani
Keyword(s):  
Solid Dispersion ◽  
Moringa Oleifera ◽  
Solid Dispersions ◽  
Intermolecular Hydrogen Bond ◽  
Thermo Gravimetric Analysis ◽  
Analytical Techniques ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Hydrogen Bond Interactions ◽  
Leaf Powder

Moringa oleifera leaf powder (MOLP) has been identified as the most important functional ingredient owing to its rich nutritional profile and healthy effects. The solubility and functional properties of this ingredient can be enhanced through solid dispersion technology. This study aimed to investigate the effects of polyethylene glycols (PEGs) 4000 and 6000 as hydrophilic carriers and solid dispersion techniques (freeze-drying, melting, solvent evaporation, and microwave irradiation) on the crystallinity and thermal stability of solid-dispersed Moringa oleifera leaf powders (SDMOLPs). SDMOLPs were dully characterized using powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), thermo-gravimetric analysis (TGA), and Fourier transform infrared spectroscopy (FTIR). The PXRD results revealed that the solid dispersions were partially amorphous with strong diffraction peaks at 2θ values of 19° and 23°. The calorimetric and thermogravimetric curves showed that PEGs conferred greater stability on the dispersions. The FTIR studyrevealed the existence of strong intermolecular hydrogen bond interactions between MOLP and PEG functional groups. MOLP solid dispersions may be useful in functional foods and beverages and nutraceutical formulations.

Decellularized liver-regenerative 3D printing biomaterials for cell-based liver therapies via a designed procedure combined with papain-containing reagent treatments and supercritical fluids

2021 ◽  
pp. 1-8
Author(s):  
Ching-Cheng Huang
Keyword(s):  
3D Printing ◽  
Thermo Gravimetric Analysis ◽  
Extraction Process ◽  
Gravimetric Analysis ◽  
Collagen Scaffolds ◽  
Scanning Calorimetry ◽  
Porcine Liver ◽  
Good Thermal Stability ◽  
Decellularized Liver ◽  
Liver Collagen

BACKGROUND: The biologic scaffolds derived from decellularized tissues and organs have been successfully developed in a variety of preclinical and/or clinical studies. OBJECTIVE: The new decellularized liver-regenerative 3D printing biomaterials were designed and prepared for cell-based liver therapies. METHODS: An extraction process was employed to remove the tissue and cellular molecules from porcine liver via pretreatment of supercritical fluid of carbon dioxide (ScCO2). Varying porosities of the decellularized liver tissues were created using papain-containing reagent treatments after ScCO2. RESULTS: The resulting liver-regenerative 3D printing biomaterials of decellularized liver collagen scaffolds were characterized by Fourier transform infrared spectroscopy, thermo-gravimetric analysis, differential scanning calorimetry and scanning electron microscopy. CONCLUSIONS: The decellularized liver collagen scaffolds with good thermal stability (>150 °C) were obtained and employed as liver-regenerative 3D printing biomaterials for cell-based liver therapies.

The Influence of Nickel Oxide Nanoparticle Dispersion on the Thermo Stability of Lubricant Oil

2019 ◽  
Vol 19 (01) ◽  
pp. 1850044
Author(s):  
K. Ramachandran ◽  
P. Navaneethakrishnan ◽  
M. Sivaraja
Keyword(s):  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
Nanoparticle Dispersion ◽  
Nio Nanoparticles ◽  
Scanning Calorimetry ◽  
Lubricant Oil ◽  
Nickel Oxide Nanoparticle ◽  
Nanoparticles Dispersion ◽  
Thermo Stability

The homogeneous and substantial dispersion of nanoparticles into base fluids is vital since the final properties of any nanolubricant are estimated by their quality of stability. This paper addresses the effect of NiO nanoparticles dispersion into SN500 lubricant oil and its nonisothermal thermo stability. The dispersion of NiO nanoparticles is achieved by ultrasonication method. The thermo stability is estimated by Thermo Gravimetric Analysis (TGA), Differential Thermal Analysis (DTA) and Differential Scanning Calorimetry (DSC). The result shows that the thermo stability of base fluid enhances up to 0.3[Formula: see text]wt.% particle concentration then it decreases due to agglomeration of dispersed nanoparticles. The findings recommend that 0.1[Formula: see text]wt.% and 0.3[Formula: see text]wt.% of NiO-nanolubricant can be used for the temperature-dependent applications up to 200∘C.

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