Feasibility Study of Chemical Treatments on Sorghum Fibres for Compatibility Enhancement in Polypropylene Composites

2018 ◽  
Vol 929 ◽  
pp. 70-77 ◽  
Author(s):  
Ismojo ◽  
Rai Pratama ◽  
Ghiska Ramahdita ◽  
Anne Zulfia Syahrial ◽  
Mochamad Chalid
Keyword(s):  
Crystallinity Index ◽  
Ester Group ◽  
Hydroxyl Group ◽  
Compatibility Study ◽  
Scanning Calorimetry ◽  
Polypropylene Composites ◽  
Dsc Measurements ◽  
Long Time ◽  
Weak Compatibility ◽  
Pp Composites

Polypropylene (PP) is one of the biggest petro-polymers, which is used in very wide application nowadays. The environment problem due to materials such as plastics having very long time degradability, and critical petroleum sources have promoted some studies to empowerment of natural resources such as natural fibres for substituting or at least modifying petro-polymers. Because of biodegradability obtained from natural source, sorghum fibers are interesting to be used as filler in PP composites, despite of weak compatibility between them. Surface modification on the sorghum fibers through alkalinization prior to acetylation was aimed to improve the fiber compatibility to PP. The treatments were expected to substitute hydroxyl group in the sorghum fibers, into acetic ester group in order to increase their hydrophobicity as the fillers. Moreover, the treatments were able to unbundle single fibers into micro-fibrillated cellulose (MFC) fibres with increase in crystallinity index. Usage of this MFC fiber as filler in PP leads to improvement of the composite performances such as thermal properties. In this study, Fourier Transformation Infra-Red (FTIR) Spectroscopy, X-ray Diffraction (XRD), Differential Scanning Calorimetry (DSC) and Field-Emission Scanning Electron Microscope (FE-SEM) were used to evaluate the performances of the Sorghum fibers after the treatments and as the filler in the Sorghum fibers/PP composites. The experimental results showed the MFC fibers as the smallest sizes in 5.0 microns and the highest crystallinity index up to 79.1 %, obtained from alkalinization with 2.5 M NaOH prior to acetylation with 17.4 M CH3COOH and the glacial (CH3CO2)2. Compatibility study of the treated Sorghum fibers on PP shows an improvement indicated by a strong interaction between the fibers and PP on morphology observation, increase in melting point of PP from 163.4°C (using virgin Shorgum fibers) into 163.6°C (using treated Sorghum fibers) in DSC measurements.

scholarly journals Compatibility Study of 1,1-Diamino-2,2-Dinitroethene (FOX-7) with Some Energetic Materials

2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Yuan-ping Zhang ◽  
Cong-hua Hou ◽  
Xin-lei Jia ◽  
Ying-xin Tan ◽  
Jing-yu Wang
Keyword(s):  
Energetic Materials ◽  
High Performance ◽  
Binary Systems ◽  
Compatibility Study ◽  
Scanning Calorimetry ◽  
Vacuum Stability ◽  
Dsc Measurements ◽  
Vacuum Stability Test ◽  
Low Sensitivity ◽  
Thermal Technique

1,1-diamino-2,2-dinitroethene (FOX-7) is a novel explosive with low sensitivity and high performance. The compatibility of FOX-7 with nine common energetic materials including hexanitrohexazaisowurtzitane (CL-20), cyclotetramethylenetetranitramine (HMX), cyclotrimethylenetrinitramine (RDX), 3,4-dinitrofurazanfuroxan (DNTF), 3-nitro-1,2,4-triazol-5-one (NTO), hexanitrostilbene (HNS-II), 2,6-diamino-3,5-dinitropyrazine-1-oxide (LLM-105), 2,4,6-triamino-1,3,5-trinitrobenzene (TATB), and 2,4,6-trinitrotoluene (TNT) were tested by differential scanning calorimetry (DSC) and the vacuum stability test (VST) as the thermal technique and X-ray diffractometry (XRD) as a nonthermal technique. DSC measurements showed that the binary systems of FOX-7/CL-20, FOX-7/HMX, FOX-7/NTO, and FOX-7/TNT were compatible in grade of A, the systems of FOX-7 with heat-resistant explosives including HNS-II, LLM-105, and TATB were compatible as well in grade of A-B, and the binary systems of FOX-7/DNTF and FOX-7/RDX had poor compatibility. VST results indicated that FOX-7 was compatible with nine energetic materials. Besides, the compatibility results of the thermal analysis were confirmed by the XRD technique.

Mechanical, thermal and dynamic-mechanical studies of functionalized halloysite nanotubes reinforced polypropylene composites

2020 ◽  
pp. 096739112096511
Author(s):  
Prakash Krishnaiah ◽  
Sivakumar Manickam ◽  
Chantara Thevy Ratnam ◽  
MS Raghu ◽  
L Parashuram ◽  
...  
Keyword(s):  
Thermal Performance ◽  
Polymer Nanocomposite ◽  
Halloysite Nanotubes ◽  
High Dispersion ◽  
Scanning Electron Micrographs ◽  
Scanning Calorimetry ◽  
Polypropylene Composites ◽  
Dynamic Mechanical ◽  
Pp Composites ◽  
Surface Modified

Mechanical, dynamic-mechanical and thermal performance of polypropylene (PP) composites which are composed of (3-Aminopropyl) triethoxysilane (APTES) functionalized Halloysite nanotubes (HNTs) were investigated. Functionalization of HNTs was confirmed by the presence of amine stretching peaks in the FTIR spectrum. A decrease in the agglomeration and high dispersion of APTES-HNTs across the PP matrix was confirmed by scanning electron micrographs (SEM). The mechanical properties of APTES-HNT-PP polymer composites were superior over their unmodified counterparts. Tensile properties such as maximum strength, Young’s modulus and impact strength were significantly enhanced by 28%, 45% and 60% respectively, with 6 wt% incorporation of surface-modified HNTs into PP matrix. A drastic improvement of stiffness and thermal stability of composites was noted with the incorporation of APTES modified HNTs into PP polymer. Differential scanning calorimetry (DSC) analysis showed a total increase of 22% in the crystallinity of clay polymer nanocomposite after filled with surface-modified HNTs. Overall, the outcome of this research confirms the modification of the surface of HNTs with a silane coupling agent, which enhances the mechanical and thermal performance of PP composites incorporated HNTs.

Surface Modification of CaCO3 Micro/Nanofillers by Pimelic Acid: Consequences on Crystallization Behaviors of Polypropylene Composites

2014 ◽  
Vol 804 ◽  
pp. 169-172
Author(s):  
Fang Wei Qi ◽  
Xue Gang Luo ◽  
Xiao Yan Lin
Keyword(s):  
Crystallization Behavior ◽  
Total Content ◽  
Growth Speed ◽  
Pimelic Acid ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Polypropylene Composites ◽  
Micro Particles ◽  
Pp Composites

In present study, two kinds of CaCO3 with micro-sized and nanometer-sized particles were treated by pimelic acid (PA) with different proportion. Then the treated particles (the total content of micro-sized and nanometer-sized CaCO3 particles was 10 wt%) were mixed with polypropylene (PP) to prepare CaCO3/PP composites by melting blending. The crystallization behavior and morphology of composites were studied by wide-angle-X-ray diffraction (WAXD), differential scanning calorimetry (DSC) and polarized microscope (PLM), respectively. Compared with PP and other samples, the content of β-crystal in the composite NCP2 where the ratio of nanoand micro particles was 2:8 (NCP2), reached the highest values. The growth speed of crystals in PP matrix was much quicker, leading to the larger spherulites than the NCP2 and NCP8. The time of complete nucleation for NCP8 was lower than PP, but higher than NCP2.

Characterization of C2H2O4 doped PVA solid polymer electrolyte

2014 ◽  
Vol 34 (9) ◽  
pp. 859-866
Author(s):  
Karur Alakanandana ◽  
Annadanam Rama Subrahmanyam ◽  
R. Sayanna ◽  
J. Siva Kumar
Keyword(s):  
Oxalic Acid ◽  
Polymer Electrolyte ◽  
Solid Polymer Electrolyte ◽  
Solid Polymer ◽  
Hydroxyl Group ◽  
Spectral Studies ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
Dsc Measurements ◽  
Absorption Studies

Abstract A novel solid polymer electrolyte based on poly vinyl alcohol (PVA) with oxalic acid was prepared by the solution caste technique. X-ray diffraction (XRD) and differential scanning calorimetry (DSC) measurements carried out on the samples clearly revealed the modification of the PVA structure; the PVA crystallinity was reduced with increasing oxalic acid content and became more amorphous. The surface morphology of these complexed polymer electrolytes was analyzed by scanning electron microscopy (SEM). Fourier transform infrared spectroscopy (FTIR) spectral studies of the samples suggested that the interaction between H+ ions of oxalic acid and oxygen of the hydroxyl group (OH) of PVA plays a major role in proton conductivity. The optical absorption studies were performed on these samples in a range of wave numbers from 200 nm to 600 nm and the optical band gap values were evaluated. Direct current (DC) conductivity was measured and temperature dependence in the range 27–273°C was studied. It was observed that the conductivity at temperatures beyond the glass transition temperature (Tg) showed a Vogel-Tamman-Fulcher (VTF) type behavior. The electrical conductivity studies on PVA with oxalic acid, in a 70:30 proportion by wt%, demonstrated that the polymer composite is a promising electrolyte for applications in electrochemical cells.

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 Sulbactam pivoxil powder attributes and compatibility study with excipients

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Loreana C. Gallo ◽  
Noelia L. Gonzalez Vidal ◽  
Fabio F. Ferreira ◽  
María V. Ramírez-Rigo
Keyword(s):  
Thermal Analyses ◽  
Oral Route ◽  
Endothermic Peak ◽  
Compatibility Study ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Thermogravimetric Curve ◽  
Almost All ◽  
Potential Interactions ◽  
Lactamase Inhibitor

Abstract Background Sulbactam pivoxil is an irreversible β-lactamase inhibitor that can be used with β-lactam antibiotics to improve antibacterial therapy by the oral route. Relevant properties of this drug for pharmaceutical manufacturing are not available in the open literature. In this work, a solid-state characterization of sulbactam pivoxil at the molecular, particle, and bulk levels was performed. Results Particles exhibited a mean diameter of about 350 μm, irregular shape crystals, and good flow properties. This work presents for the first time the crystal structure of this β-lactamase inhibitor obtained by X-ray diffraction analysis. Fourier-transform infrared results showed the characteristic bands of aliphatic hydrocarbons and ester groups. The differential scanning calorimetry curve exhibited a sharp endothermic peak at 109 °C corresponding to sulbactam pivoxil melting. The thermogravimetric curve revealed a mass loss at 184 °C associated with a decomposition process. This powder showed a moisture content of 0.34% and a water activity of 0.463. Potential interactions between sulbactam pivoxil and common pharmaceutical excipients were evaluated by thermal analysis. The endothermic peak and the enthalpies of melting were preserved in almost all the analyzed mixtures. Conclusion The powder was constituted by micro-sized crystals of sulbactam pivoxil that had suitable physicochemical properties for processing in controlled humidity environments. Thermal analyses suggested that sulbactam pivoxil is compatible with most of the evaluated excipients. The information obtained in the present study is relevant for the development, manufacturing, and storage of formulations that include sulbactam pivoxil.

scholarly journals Enhancement of Antioxidant and Hydrophobic Properties of Alginate via Aromatic Derivatization: Preparation, Characterization, and Evaluation

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2575
Author(s):  
Smaher M. Elbayomi ◽  
Haili Wang ◽  
Tamer M. Tamer ◽  
Yezi You
Keyword(s):  
Radical Scavenging Activity ◽  
Radical Scavenging ◽  
Hydroxyl Group ◽  
Hydroxyl Groups ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Benzoyl Group ◽  
Antioxidant Evaluation ◽  
Thermo Stability

The preparation of bioactive polymeric molecules requires the attention of scientists as it has a potential function in biomedical applications. In the current study, functional substitution of alginate with a benzoyl group was prepared via coupling its hydroxyl group with benzoyl chloride. Fourier transform infrared spectroscopy indicated the characteristic peaks of aromatic C=C in alginate derivative at 1431 cm−1. HNMR analysis demonstrated the aromatic protons at 7.5 ppm assigned to benzoyl groups attached to alginate hydroxyl groups. Wetting analysis showed a decrease in hydrophilicity in the new alginate derivative. Differential scanning calorimetry and thermal gravimetric analysis showed that the designed aromatic alginate derivative demonstrated higher thermo-stability than alginates. The aromatic alginate derivative displayed high anti-inflammatory properties compared to alginate. Finally, the in vitro antioxidant evaluation of the aromatic alginate derivative showed a significant increase in free radical scavenging activity compared to neat alginate against DPPH (2,2-diphenyll-picrylhydrazyl) and ABTS free radicals. The obtained results proposed that the new alginate derivative could be employed for gene and drug delivery applications.

scholarly journals Polypropylene/Lignin/POSS Nanocomposites: Thermal and Wettability Properties, Application in Water Remediation

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3950
Author(s):  
Abeer Alassod ◽  
Syed Rashedul Islam ◽  
Mina Shahriari Khalaji ◽  
Rogers Tusiime ◽  
Wanzhen Huang ◽  
...  
Keyword(s):  
Organic Liquid ◽  
Contact Angles ◽  
Water Remediation ◽  
Scanning Calorimetry ◽  
Water Contact ◽  
Thermally Induced ◽  
Dsc Measurements ◽  
Infrared Measurement ◽  
Oligomeric Silsesquioxane ◽  
Tga And Dsc

Compositing is an interesting strategy that has always been employed to introduce or enhance desired functionalities in material systems. In this paper, sponges containing polypropylene, lignin, and octavinyl-polyhedral oligomeric silsesquioxane (OV-POSS) were successfully prepared via an easy and elegant strategy called thermally induced phase separation (TIPS). To fully explore the behaviour of different components of prepared sponges, properties were characterized by a thermogravimetric analyser (TGA), differential scanning calorimetry (DSC), Fourier transform infrared measurement (FTIR), and scanning electron microscopy (SEM). Furthermore, wettability properties toward an organic liquid and oil were investigated. The FTIR analysis confirmed the chemical modification of the components. TGA and DSC measurements revealed thermal stability was much better with an increase in OV-POSS content. OV-POSS modified sponges exhibited ultra-hydrophobicity and high oleophilicity with water contact angles of more than 125°. The SEM revealed that POSS molecules acted as a support for reduced surface roughness. Moreover, OV-POSS-based blend sponges showed higher sorption capacities compared with other blend sponges without OV-POSS. The new blend sponges demonstrated a potential for use as sorbent engineering materials in water remediation.

scholarly journals Improving the mechanical properties of polypropylene composites with coconut shell particles

2021 ◽  
Vol 30 ◽  
pp. 263498332110074
Author(s):  
Henry C Obasi ◽  
Uchechi C Mark ◽  
Udochukwu Mark
Keyword(s):  
Mechanical Properties ◽  
Particle Size ◽  
Flexural Modulus ◽  
Filler Particle ◽  
Tensile Modulus ◽  
Coconut Shell ◽  
Polypropylene Composites ◽  
Increase With Increase ◽  
Pp Composites ◽  
Shell Particles

Conventional inorganic fillers are widely used as fillers for polymer-based composites. Though, their processing difficulties and cost have demanded the quest for credible alternatives of organic origin like coconut shell fillers. Dried shells of coconut were burnt, ground, and sifted to sizes of 63, 150, 300, and 425 µm. The ground coconut shell particles (CSP) were used as a filler to prepare polypropylene (PP) composites at filler contents of 0% to 40% via injection melt blending process to produce PP composite sheets. The effect of the filler particle size on the mechanical properties was investigated. The decrease in the size of filler (CSP) was found to improve the yield strength, tensile strength, tensile modulus, flexural strength, flexural modulus, and hardness of PP by 8.5 MPa, 15.75 MPa, 1.72 GPa, 7.5 MPa, 100 MPa, and 10.5 HR for 63 µm at 40%, respectively. However, the elongation at break and modulus of resilience of the PP composites were seen to increase with increase in the filler size. Scanning electron microscope analysis showed that fillers with 63 µm particle size had the best distribution and interaction with the PP matrix resulting in enhanced properties.

scholarly journals Accelerated aging of WPCs Based on Polypropylene and Birch plywood Sanding Dust

2021 ◽  
Vol 11 (1) ◽  
pp. 319-328
Author(s):  
Janis Kajaks ◽  
Karlis Kalnins ◽  
Juris Matvejs
Keyword(s):  
Accelerated Aging ◽  
Degree Of Crystallinity ◽  
Accelerated Weathering ◽  
Recrystallization Process ◽  
Surface Layers ◽  
Uv Aging ◽  
Polypropylene Composites ◽  
Weathering Processes ◽  
Melting Temperatures ◽  
Dsc Measurements

Abstract A lot of researchers are closely related with natural, lignocellulose fibre containing bio-composites production and studies. Various of polymer matrices, mainly polyolefins, combinations with natural fibres as a reinforcement are used. Our studies are focused on polypropylene based bio-composites containing birch plywood production by-product sanding dust (PSD) accelerated weathering processes. The obtained results showed the following sight. After the aging the surface of all samples had faded, the changes of the gloss (decreasing) and of the whiteness degree (increasing) also had taken place, but microhardness of the surface of specimens significantly has decreased. The tensile strength and modulus of the samples after UV aging diminished about 30–35%. That indicates to the changes not only in the surface layers of polymer but also inside of the polymer structure. The FTIR measurements showed that during UV aging process occurs significant changes of chemical structure of the weathered surface of all samples. DSC measurements showed an increase of degree of crystallinity of the weathered polypropylene composites after the first heating due to the recrystallization process in the polypropylene matrix and a small decreasing after second heating. The melting temperatures of all composites after UV aging considerably diminish up to 30°C.

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