scholarly journals Effect of Wood Fiber Loading on the Chemical and Thermo-Rheological Properties of Unrecycled and Recycled Wood-Polymer Composites

2020 ◽  
Vol 10 (24) ◽  
pp. 8863
Author(s):  
Klementina Pušnik Črešnar ◽  
Lidija Fras Zemljič ◽  
Lidija Slemenik Perše ◽  
Marko Bek
Keyword(s):  
Rheological Properties ◽  
Wood Fiber ◽  
Xrd Analysis ◽  
Attenuated Total Reflection ◽  
Material Behavior ◽  
Degree Of Crystallinity ◽  
Scanning Calorimetry ◽  
Wood Polymer ◽  
3D Network ◽  
Pp Composites

Novel wood fiber (WF)-polypropylene composites were developed using the extrusion process with a twin-screw extruder. The influence of different mass addition of WF to unrecycled polypropylene (PP) and recycled PP (R-PP) on the chemical, thermal and rheological properties of the processed WF-PP and WF-R-PP composites was investigated. For this purpose, the chemical surface structure of the composites was followed with ATR-FTIR (attenuated total reflection Fourier transform infra red spectroscopy), while the thermal properties of the WF-PP composites were investigated with differential scanning calorimetry (DSC). Furthermore, the crystalline structure of the composites was determined by X-ray diffraction (XRD) analysis. Finally, the rheology of the materials was also studied. It was observed that a stronger particle formation at high additional concentrations was observed in the case of recycled PP material. The addition of WF over 20% by weight increased the crystallinity as a result of the incorporation and reorganization of the WF and also their reinforcing effect. The addition of WF to pure PP had an influence on the crystallization process, which due to the new β phase and γ phase PP formation showed an increased degree of crystallinity of the composites and led to a polymorphic structure of the composites WF-PP. From the rheological test, we can conclude that the addition of WF changed the rheological behavior of the material, as WF hindered the movement of the polymeric material. At lower concentrations, the change was less pronounced, although we observed more drastic changes in the material behavior at concentrations high enough that WF could form a 3D network (percolation point about 20%).

Magnetic Properties of Irradiated Nickel Ferrite Thermoplastic Natural Rubber Nanocomposite

2014 ◽  
Vol 879 ◽  
pp. 206-212 ◽  
Author(s):  
Sivanesan Appadu ◽  
Sahrim Hj. Ahmad ◽  
Chantara Thevy Ratnam ◽  
Meor Yahaya Razali ◽  
Moayad Husein Flaifel ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Thermal Properties ◽  
Natural Rubber ◽  
Weight Ratio ◽  
Xrd Analysis ◽  
Degree Of Crystallinity ◽  
Scanning Calorimetry ◽  
Magnetic Microstructure ◽  
Sem Image ◽  
Thermoplastic Natural Rubber

The effect of electron beam (EB) irradiation at different doses on the magnetic, microstructure, morphological and thermal properties of NiFe2O4/Thermoplastic Natural Rubber (TPNR) nanocomposite was investigated. The NiFe2O4/TPNR nanocomposite samples were prepared by using a Haake mixer in weight ratio of 12:88. The TPNR matrix consists of natural rubber (NR), liquid natural rubber (LNR) and high density polyethylene (HDPE) in weight ratio of 20:10:70. The samples were irradiated using a 2 MeV EB machine in doses from 0 - 200 kGy. Magnetic properties studied by using the vibrating sample magnetometer (VSM) at room temperature showed that the values of saturation magnetization (MS), remanence magnetization (MR) and the coercivity (HC) value increased with increasing doses of irradiation. The increase in MSand MRvalues is attributed to the increase in concentration of Fe3+ions at octahedral B-site and decrease of concentration at the tetrahedral A-site in the NiFe2O4cubic structure. X-ray diffraction (XRD) analysis of the samples showed that peak intensities decreased and the width of the peaks increased with increasing doses of irradiation. Scanning electron microscope (SEM) image of the nanocomposite cross section showed the presence of defects which is more visible with increasing doses of irradiation. In the case of thermal properties, differential scanning calorimetry (DSC) analysis showed that the crystallization temperature (Tc) and the degree of crystallinity (Xc) of the nanocomposite samples decreased with increasing doses of irradiation due to crosslinking of polymeric chains which hinders the growth of crystals.

Effects of surface modification of halloysite nanotubes on the morphology and the thermal and rheological properties of polypropylene/halloysite composites

2018 ◽  
Vol 38 (2) ◽  
pp. 119-127 ◽  
Author(s):  
Xiaochun Yin ◽  
Liang Wang ◽  
Sai Li ◽  
Guangjian He ◽  
Zhitao Yang
Keyword(s):  
Thermal Stability ◽  
Fourier Transform ◽  
Rheological Properties ◽  
Thermal Analyses ◽  
Halloysite Nanotubes ◽  
Degree Of Crystallinity ◽  
Dynamic Shear ◽  
Extensional Deformation ◽  
Pp Composites ◽  
The Degree Of Crystallinity

AbstractEffects of unmodified halloysite nanotubes (HNTs) and hexadecyl trimethyl ammonnium bromide treated halloysite nanotubes (CTAB-HNTs) on the morphology as well as the thermal and rheological properties of the HNT-filled polypropylene (PP) composites were investigated. The composites were melt-blended with a novel vane mixer dominated by extensional deformation. Fourier transform infrared spectroscopy well demonstrated that ammonium molecules were successfully interacted with halloysite groups. Compared with unmodified HNTs, the modified HNTs had a better dispersion in the PP matrix. The degree of crystallinity increased with the introduction of HNTs into the PP matrix. Thermal analyses revealed that CTAB-HNTs can improve the composites’ thermal stability compared with unmodified HNTs. As for dynamic shear rheology, the PP/CTAB-HNT composites showed higher viscoelaticity than neat PP in most frequency regimes, and that the raw HNT/PP composites presented the opposite phenomenon. The relaxation time of PP melt and the availability of heterogeneous PP domains increased with the presence of CTAB-HNTs.

scholarly journals Insight into the Surface Properties of Wood Fiber-Polymer Composites

Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1535
Author(s):  
Klementina Pušnik Črešnar ◽  
Marko Bek ◽  
Thomas Luxbacher ◽  
Mihael Brunčko ◽  
Lidija Fras Zemljič
Keyword(s):  
Polymer Composites ◽  
Surface Properties ◽  
Wood Fiber ◽  
Antioxidant Properties ◽  
Skin Layer ◽  
Filler Loading ◽  
Attenuated Total Reflection ◽  
Thermoplastic Composites ◽  
Wood Fibers ◽  
Pp Composites

The surface properties of wood fiber (WF) filled polymer composites depend on the filler loading and are closely related to the distribution and orientation in the polymer matrix. In this study, wood fibers (WF) were incorporated into thermoplastic composites based on non-recycled polypropylene (PP) and recycled (R-PP) composites by melt compounding and injection moulding. ATR-FTIR (attenuated total reflection Fourier transform infrared spectroscopy) measurements clearly showed the propagation of WF functional groups at the surface layer of WF-PP/WF-R-PP composites preferentially with WF loading up to 30%. Optical microscopy and nanoindentation method confirmed the alignment of thinner skin layer of WF-PP/WF-R-PP composites with increasing WF addition. The thickness of the skin layer was mainly influenced by the WF loading. The effect of the addition of WF on modulus and hardness, at least at 30 and 40 wt.%, varies for PP and R-PP matrix. On the other hand, surface zeta potential measurements show increased hydrophilicity with increasing amounts of WF. Moreover, WF in PP/R-PP matrix is also responsible for the antioxidant properties of these composites as measured by DPPH (2,2′-diphenyl-1-picrylhydrazyl) assay.

The Attenuated Total Reflection Infrared Analysis of Surface Crystallinity of Polyhydroxyalkanoates

e-Polymers ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Shinn-Gwo Hong ◽  
Wei-Ming Chen
Keyword(s):  
Surface Layer ◽  
Petri Dish ◽  
Weight Percent ◽  
Total Reflection ◽  
Attenuated Total Reflection ◽  
Degree Of Crystallinity ◽  
Infrared Analysis ◽  
Scanning Calorimetry ◽  
Solvent Cast ◽  
Penetration Depths

AbstractThe surface crystallization of three different polyhydroxy alkanoates (PHAs), poly(3-hydroxybutyrate) (PHB), PHB-co-5 weight percent 3-hydroxyvalerate (PHBV5), and PHB-co-12 weight percent 3- hydroxyvalerate (PHBV12), under different processing conditions is analyzed with depth profiling attenuated total reflection spectroscopy (ATR) and differential scanning calorimetry (DSC). The results of ATR indicate that there is a crystallinity distribution on the outer 2 microns thick surface layer. The degree of crystallinity in different penetration depths follows the order of 0.92μ > 0.41μ > 1.70μ for all three hot-pressed PHAs studied and the outer surfaces have a much greater crystallinity than the bulk. The surface crystallinity of specimens is in the order of PHB > PHBV5 > PHBV12 regardless of the different penetration depths analyzed which is consistent with the DSC results. It is also obtained that the effect of annealing in enhancing the crystallization of PHAs is more significant in the surface layer. The surface crystallinity of PHAs obtained after annealing follows the trend of Petri-dish side of solvent-cast PHB > hotpress PHB > air side of solvent-cast PHB > PHBV5 > PHBV12. The difference in crystallinity between the surface and the bulk of PHAs decreases with the addition of 3-hydroxyvalerate but increases after annealing. It is confirmed that the film forming method and the substrate contacted affect the surface crystalline state of PHAs which is attributed to the changes in crystallization conditions in the surface materials.

scholarly journals POLYAMIDE 11 POROUS FILMS BY NIPS: THE INFLUENCE OF MISCIBILITY AND POLYMER CRYSTALLINE FORMATION IN PORES STRUCTURE AND MORPHOLOGY

Química Nova ◽  
2021 ◽  
Author(s):  
Rayanne Lima ◽  
Thieres Pereira ◽  
Eloi Silva Filho
Keyword(s):  
Ternary Phase Diagram ◽  
Polymer Concentration ◽  
Strain Analysis ◽  
Xrd Analysis ◽  
Polymer Composition ◽  
Degree Of Crystallinity ◽  
Porous Films ◽  
Scanning Calorimetry ◽  
Stress Strain ◽  
Polyamide 11

This study described the morphology, crystallinity, thermal and mechanical characterization of Polyamide 11 (PA11) porous film prepared by non-solvent induced phase separation (NIPS) method using formic acid (FA) as solvent. In addition, the miscibility of PA11/FA/H2O system was performed to generate a ternary phase diagram. The porous films morphology was investigated by Scanning Electronic Microscopy (SEM) analysis, the crystallinity by X-Ray Diffractometer (XRD) and thermal study by Differential Scanning Calorimetry (DSC). A cellulosic reinforcement was used in porous films and the stress-strain analysis was performance by Dynamic Mechanical Analysis (DMA). The porous films were prepared with polymer composition of 15, 20 and 25 wt%. The porous films showed different microstructure in function of polymer concentration. The 20 and 25 wt% porous films showed micropores structures with medium pores diameters between 0-10µm calculated by image analysis. The XRD analysis show predominance of α crystalline form of polymer at 20 and 25 wt% porous films. The degree of crystallinity increases with polymer concentration increase. The stress-strain analysis of porous films shows a proportional dependence of Young’s modulus with the increase of polymer concentration in each film.

Mannose Conjugated Starch Nanoparticles for Preferential Targeting of Liver Cancer

2020 ◽  
Vol 17 ◽  
Author(s):  
Akhlesh Kumar Jain ◽  
Hitesh Sahu ◽  
Keerti Mishra ◽  
Suresh Thareja
Keyword(s):  
Side Effects ◽  
Liver Cancer ◽  
Entrapment Efficiency ◽  
Xrd Analysis ◽  
In Vitro Cytotoxicity ◽  
Physical Interaction ◽  
Scanning Calorimetry ◽  
Starch Nanoparticles

Aim: To design D-Mannose conjugated 5-Fluorouracil (5-FU) loaded Jackfruit seed starch nanoparticles (JFSSNPs) for site specific delivery. Background: Liver cancer is the third leading cause of death in world and fifth most often diagnosed cancer is the major global threat to public health. Treatment of liver cancer with conventional method bears several side effects, thus to undertake these side effects as a formulation challenge, it is necessary to develop novel target specific drug delivery system for the effective and better localization of drug into the proximity of target with restricting the movement of drug in normal tissues. Objective: To optimize and characterize the developed D-Mannose conjugated 5-Fluorouracil (5-FU) loaded Jackfruit seed starch nanoparticles (JFSSNPs) for effective treatment of liver cancer. Materials and methods: 5-FU loaded JFSSNPs were prepared and optimized formulation had higher encapsulation efficiency were conjugated with D-Mannose. These formulations were characterized for size, morphology, zeta potential, X-Ray Diffraction, and Differential Scanning Calorimetry. Potential of NPs were studied using in vitro cytotoxicity assay, in vivo kinetic studies and bio-distribution studies. Result and discussion: 5-Fluorouracil loaded NPs had particle size between 336 to 802nm with drug entrapment efficiency was between 64.2 to 82.3%. In XRD analysis, 5-FU peak was diminished in the diffractogram, which could be attributed to the successful incorporation of drug in amorphous form. DSC study suggests there was no physical interaction between 5- FU and Polymer. NPs showed sustained in vitro 5-FU release up to 2 hours. In vivo, mannose conjugated NPs prolonged the plasma level of 5-FU and assist selective accumulation of 5-FU in the liver (vs other organs spleen, kidney, lungs and heart) compared to unconjugated one and plain drug. Conclusion: In vivo, bio-distribution and plasma profile studies resulted in significantly higher concentration of 5- Fluorouracil liver suggesting that these carriers are efficient, viable, and targeted carrier of 5-FU treatment of liver cancer.

scholarly journals PEG-POSS Star Molecules Blended in Polyurethane with Flexible Hard Segments: Morphology and Dynamics

Molecules ◽  
2020 ◽  
Vol 26 (1) ◽  
pp. 99
Author(s):  
Konstantinos N. Raftopoulos ◽  
Edyta Hebda ◽  
Anna Grzybowska ◽  
Panagiotis A. Klonos ◽  
Apostolos Kyritsis ◽  
...  
Keyword(s):  
Glass Transition ◽  
Star Polymer ◽  
Polymerization Process ◽  
Degree Of Crystallinity ◽  
Dielectric Relaxation Spectroscopy ◽  
Scanning Calorimetry ◽  
Similar System ◽  
Soft Phase ◽  
Hard Segments ◽  
Star Molecules

A star polymer with a polyhedral oligomeric silsesquioxanne (POSS) core and poly(ethylene glycol) (PEG) vertex groups is incorporated in a polyurethane with flexible hard segments in-situ during the polymerization process. The blends are studied in terms of morphology, molecular dynamics, and charge mobility. The methods utilized for this purpose are scanning electron and atomic force microscopies (SEM, AFM), X-ray diffraction (XRD), differential scanning calorimetry (DSC), and to a larger extent dielectric relaxation spectroscopy (DRS). It is found that POSS reduces the degree of crystallinity of the hard segments. Contrary to what was observed in a similar system with POSS pendent along the main chain, soft phase calorimetric glass transition temperature drops as a result of plasticization, and homogenization of the soft phase by the star molecules. The dynamic glass transition though, remains practically unaffected, and a hypothesis is formed to resolve the discrepancy, based on the assumption of different thermal and dielectric responses of slow and fast modes of the system. A relaxation α′, slower than the bulky segmental α and common in polyurethanes, appears here too. A detailed analysis of dielectric spectra provides some evidence that this relaxation has cooperative character. An additional relaxation g, which is not commonly observed, accompanies the Maxwell Wagner Sillars interfacial polarization process, and has dynamics similar to it. POSS is found to introduce conductivity and possibly alter its mechanism. The study points out that different architectures of incorporation of POSS in polyurethane affect its physical properties by different mechanisms.

scholarly journals Recycling Waste Cotton Cloths for the Isolation of Cellulose Nanocrystals: A Sustainable Approach

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 626
Author(s):  
Siti Hajar Mohamed ◽  
Md. Sohrab Hossain ◽  
Mohamad Haafiz Mohamad Kassim ◽  
Mardiana Idayu Ahmad ◽  
Fatehah Mohd Omar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Cellulose Nanocrystals ◽  
Value Added ◽  
Crystallinity Index ◽  
Attenuated Total Reflection ◽  
Cellulose Content ◽  
Scanning Calorimetry ◽  
Good Thermal Stability ◽  
Alkaline Pulping ◽  
Hydrolysis Of Cellulose

There is an interest in the sustainable utilization of waste cotton cloths because of their enormous volume of generation and high cellulose content. Waste cotton cloths generated are disposed of in a landfill, which causes environmental pollution and leads to the waste of useful resources. In the present study, cellulose nanocrystals (CNCs) were isolated from waste cotton cloths collected from a landfill. The waste cotton cloths collected from the landfill were sterilized and cleaned using supercritical CO2 (scCO2) technology. The cellulose was extracted from scCO2-treated waste cotton cloths using alkaline pulping and bleaching processes. Subsequently, the CNCs were isolated using the H2SO4 hydrolysis of cellulose. The isolated CNCs were analyzed to determine the morphological, chemical, thermal, and physical properties with various analytical methods, including attenuated total reflection-Fourier transform-infrared spectroscopy (ATR-FTIR), field-emission scanning electron microscopy (FE-SEM), energy-filtered transmission electron microscopy (EF-TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The results showed that the isolated CNCs had a needle-like structure with a length and diameter of 10–30 and 2–6 nm, respectively, and an aspect ratio of 5–15, respectively. Additionally, the isolated CNCs had a high crystallinity index with a good thermal stability. The findings of the present study revealed the potential of recycling waste cotton cloths to produce a value-added product.

scholarly journals Crystallization Behavior and Mechanical Properties of Poly(ε-caprolactone) Reinforced with Barium Sulfate Submicron Particles

Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2368
Author(s):  
Hegoi Amestoy ◽  
Paul Diego ◽  
Emilio Meaurio ◽  
Jone Muñoz ◽  
Jose-Ramon Sarasua
Keyword(s):  
Barium Sulfate ◽  
Thermal Studies ◽  
Polarized Light ◽  
Optical Microscope ◽  
Submicron Particles ◽  
Degree Of Crystallinity ◽  
Scanning Calorimetry ◽  
Nucleation Effect ◽  
Crystal Fraction ◽  
Light Optical Microscope

Poly(ε-caprolactone) (PCL) was mixed with submicron particles of barium sulfate to obtain biodegradable radiopaque composites. X-ray images comparing with aluminum samples show that 15 wt.% barium sulfate (BaSO4) is sufficient to present radiopacity. Thermal studies by differential scanning calorimetry (DSC) show a statistically significant increase in PCL degree of crystallinity from 46% to 52% for 25 wt.% BaSO4. Non-isothermal crystallization tests were performed at different cooling rates to evaluate crystallization kinetics. The nucleation effect of BaSO4 was found to change the morphology and quantity of the primary crystals of PCL, which was also corroborated by the use of a polarized light optical microscope (PLOM). These results fit well with Avrami–Ozawa–Jeziorny model and show a secondary crystallization that contributes to an increase in crystal fraction with internal structure reorganization. The addition of barium sulfate particles in composite formulations with PCL improves stiffness but not strength for all compositions due to possible cavitation effects induced by debonding of reinforcement interphase.

scholarly journals The Influence of the Addition of Nuts on the Thermal and Rheological Properties of Wheat Flour

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3969
Author(s):  
Karolina Pycia ◽  
Lesław Juszczak
Keyword(s):  
Rheological Properties ◽  
Wheat Flour ◽  
Viscoelastic Properties ◽  
Control Sample ◽  
Scanning Calorimetry ◽  
Creep And Recovery ◽  
Research Material ◽  
Pasting Characteristics ◽  
Tan Δ ◽  
Weak Gels

The aim of the study was to assess the influence of replacing wheat flour with hazelnuts or walnuts, in various amounts, on the thermal and rheological properties of the obtained systems. The research material were systems in which wheat flour was replaced with ground hazelnuts (H) or walnuts (W) in the amount of 5%, 10%, and 15%. The parameters of the thermodynamic gelatinization characteristics were determined by the differential scanning calorimetry method. In addition, the pasting characteristics were determined with the use of a viscosity analyzer and the viscoelastic properties were assessed. Sweep frequency and creep and recovery tests were used to assess the viscoelastic properties of the tested gels. It was found that replacing wheat flour with nuts increased the values of gelatinization temperature, gelatinization, and retrogradation enthalpy, and the degree of retrogradation. The highest viscosity was characteristic of the control sample (2039 mPa·s), and the lowest for the paste with 15% addition of walnuts (1120 mPa·s). Replacing the flour with nuts resulted in a very visible reduction in the viscosity of such systems. In addition, gels based on the systems with the addition of H and W were weak gels (tan δ = G″/G′ > 0.1), and the values of G′ and G″ parameters decreased with the increased share of nuts in the systems. Creep and recovery analysis indicated that the systems in which wheat flour was replaced with hazelnuts were less susceptible to deformation compared to the systems with the addition of W.

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