Construction of polypropylene composite multifilaments filled with sodium perborate trihydrate-treated jute microparticles

2017 ◽  
Vol 24 (2) ◽  
pp. 203-212 ◽  
Author(s):  
Yasemin Seki ◽  
Aysun Akşit ◽  
Umit Halis Erdoğan
Keyword(s):  
Photoelectron Spectroscopy ◽  
Textile Industry ◽  
Melt Spinning ◽  
Moisture Absorption ◽  
Nucleating Agent ◽  
Sodium Perborate ◽  
Polypropylene Composite ◽  
Scanning Calorimetry ◽  
Vertical Wicking ◽  
Potential Applications

AbstractPolypropylene composite multifilaments filled with surface-treated jute microparticles were successfully spun by melt spinning. To enhance the particle distribution, jute particleos were treated with 5–20% (w/v) aqueous solutions of sodium perborate trihydrate (SP). X-ray photoelectron spectroscopy (XPS) was used to confirm the surface treatment. XPS analysis indicated that the treatments improved the hydrophobicity of the jute by means of increasing the carbon/oxygen ratio of the surface; thus, the maximum increment was achieved after 10% (w/v) SP treatment. After determining the optimum SP concentration, the spinning of polypropylene composite multifilaments containing 0.3–1.4 wt% jute particles was employed. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) revealed the nucleating agent effect of the particles during crystallization in the filaments. The addition of fillers did not result in significant changes in the functional groups of polypropylene. The main output of this research is that polypropylene multifilaments incorporating 1.4 wt% jute particles presented the highest moisture absorption and hydrophilic character as determined by TGA, moisture content, and vertical wicking tests. It was concluded that particle content >0.3 wt% showed a tendency to agglomerate in the filament. Consequently, this study provided a new polypropylene filament having moisture absorbability performance, which can create potential applications in the textile industry.

Novel shape-memory polyurethane fibers for textile applications

2018 ◽  
Vol 89 (6) ◽  
pp. 1027-1037 ◽  
Author(s):  
Míriam Sáenz-Pérez ◽  
Tariq Bashir ◽  
José Manuel Laza ◽  
Jorge García-Barrasa ◽  
José Luis Vilas ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Shape Memory ◽  
Tensile Testing ◽  
Melt Spinning ◽  
Mechanical Analysis ◽  
Knitted Fabric ◽  
Scanning Calorimetry ◽  
Moisture Management ◽  
Potential Applications ◽  
Shape Memory Polyurethane

In this work, thermoresponsive shape-memory polyurethane (SMPU) fibers were produced by melt spinning from different SMPU pellets. Afterwards, the knitted fabric samples were prepared by the obtained fibers. Some of the SMPUs used were synthesized previously in our laboratory whereas a commercial one, named DIAPLEX MM4520, was also evaluated in order to carry out comparative studies. All the SMPUs were characterized by different techniques, such as thermogravimetric analysis, differential scanning calorimetry, dynamic mechanical analysis and tensile testing. Moreover, the shape-memory capabilities of the fabrics were measured by thermo-mechanical analysis. The obtained results show that the synthesized SMPUs could be attractive candidates for potential applications such as breathable fabrics or moisture-management textiles.

scholarly journals Impact of the Fused Deposition (FDM) Printing Process on Polylactic Acid (PLA) Chemistry and Structure

2017 ◽  
Author(s):  
Michael Cuiffo ◽  
Jeffrey Snyder ◽  
Alicia Elliott ◽  
Nicholas Romero ◽  
Sandhiya Kannan ◽  
...  
Keyword(s):  
Ftir Spectroscopy ◽  
Polylactic Acid ◽  
Photoelectron Spectroscopy ◽  
Source Material ◽  
Organic Polymer ◽  
Spectroscopic Techniques ◽  
Scanning Calorimetry ◽  
Fused Deposition ◽  
Hygroscopic Nature ◽  
Potential Applications

Polylactic Acid (PLA) is an organic polymer commonly used in fused deposition (FDM) printing and biomedical scaffolding that is biocompatible and immunologically inert. However, variations in source material quality and chemistry make it necessary to characterize the filament and determine potential changes in chemistry occurring as a result of the FDM process. We used several spectroscopic techniques, including laser confocal microscopy, Fourier-Transform Infrared (FTIR) spectroscopy and photoacousitc FTIR spectroscopy, Raman spectroscopy, and X-ray photoelectron Spectroscopy (XPS) in order to characterize both the bulk and surface chemistry of the source material and printed samples. Scanning Electron Microscopy (SEM) and Differential Scanning Calorimetry (DSC) were used to characterize morphology, crystallinity, and the glass transition temperature following printing. Analysis revealed calcium carbonate-based additives which were reacted with organic ligands and potentially trace metal impurities, both before and following printing. These additives became concentrated in voids in the printed structure. This finding is important for biomedical applications as carbonate will impact subsequent cell growth on printed tissue scaffolds. Results of chemical analysis also provided evidence of the hygroscopic nature of the source material and oxidation of the printed surface, and SEM imaging revealed micro and sub-micron scale roughness that will also impact potential applications.

Graphene nanocomposites: A review on processes, properties, and applications

2021 ◽  
pp. 152808372110242
Author(s):  
Kadir Bilisik ◽  
Mahmuda Akter
Keyword(s):  
Textile Industry ◽  
In Situ Polymerization ◽  
Resin Transfer Molding ◽  
Single Layer ◽  
Chemical Vapor ◽  
Synthesis Process ◽  
Graphene Nanocomposites ◽  
Transfer Molding ◽  
Potential Applications ◽  
Nano Graphene

In this paper, graphene, graphene/matrix, and graphene/fiber nanocomposites, including their synthesis process, fabrication, properties, and potential applications, were reviewed. It was found that several synthesis techniques for nanographene were developed, such as liquid-phase exfoliation and chemical vapor deposition. In addition, some fabrication processes of graphene/matrix and graphene/fiber-based nanocomposites were made, including in-situ polymerization, nanostitching in that single layer nano graphene plate could be interconnected by means of carbon nanotube stitching, resin transfer molding, and vacuum-assisted resin transfer molding. Several properties, including mechanical, thermal, and electrical, on the graphene nanoplatelets materials were summarized in this review paper. It was realized that graphene, graphene/matrix, and graphene/fiber nanocomposites have extraordinary mechanical, thermal, and electrical properties used in advanced engineering applications, including soft robotics, microelectronics, energy storage, biomedical and biosensors as well as textile industry.

scholarly journals Dynamic Single-Fiber Pull-Out of Polypropylene Fibers Produced with Different Mechanical and Surface Properties for Concrete Reinforcement

Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 722
Author(s):  
Enrico Wölfel ◽  
Harald Brünig ◽  
Iurie Curosu ◽  
Viktor Mechtcherine ◽  
Christina Scheffler
Keyword(s):  
Tensile Strength ◽  
Dynamic Loading ◽  
Melt Spinning ◽  
Structural Changes ◽  
High Surface ◽  
Single Fiber ◽  
Scanning Calorimetry ◽  
Matrix Interaction ◽  
Pull Out ◽  
Fiber Matrix

In strain-hardening cement-based composites (SHCC), polypropylene (PP) fibers are often used to provide ductility through micro crack-bridging, in particular when subjected to high loading rates. For the purposeful material design of SHCC, fundamental research is required to understand the failure mechanisms depending on the mechanical properties of the fibers and the fiber–matrix interaction. Hence, PP fibers with diameters between 10 and 30 µm, differing tensile strength levels and Young’s moduli, but also circular and trilobal cross-sections were produced using melt-spinning equipment. The structural changes induced by the drawing parameters during the spinning process and surface modification by sizing were assessed in single-fiber tensile experiments and differential scanning calorimetry (DSC) of the fiber material. Scanning electron microscopy (SEM), atomic force microscopy (AFM) and contact angle measurements were applied to determine the topographical and wetting properties of the fiber surface. The fiber–matrix interaction under quasi-static and dynamic loading was studied in single-fiber pull-out experiments (SFPO). The main findings of microscale characterization showed that increased fiber tensile strength in combination with enhanced mechanical interlocking caused by high surface roughness led to improved energy absorption under dynamic loading. Further enhancement could be observed in the change from a circular to a trilobal fiber cross-section.

Effect of toughened polyamide-coated carbon fiber fabric on the mechanical performance and fracture toughness of CFRP

2021 ◽  
pp. 002199832199945
Author(s):  
Jong H Eun ◽  
Bo K Choi ◽  
Sun M Sung ◽  
Min S Kim ◽  
Joon S Lee
Keyword(s):  
Mechanical Properties ◽  
Fracture Toughness ◽  
Photoelectron Spectroscopy ◽  
Mechanical Performance ◽  
Epoxy Composites ◽  
Scanning Calorimetry ◽  
Internal Damage ◽  
Impact Tests ◽  
Flexural Tests ◽  
The Impact

In this study, carbon/epoxy composites were manufactured by coating with a polyamide at different weight percentages (5 wt.%, 10 wt.%, 15 wt.%, and 20 wt.%) to improve their impact resistance and fracture toughness. The chemical reaction between the polyamide and epoxy resin were examined by fourier transform infrared spectroscopy, differential scanning calorimetry and X-ray photoelectron spectroscopy. The mechanical properties and fracture toughness of the carbon/epoxy composites were analyzed. The mechanical properties of the carbon/epoxy composites, such as transverse flexural tests, longitudinal flexural tests, and impact tests, were investigated. After the impact tests, an ultrasonic C-scan was performed to reveal the internal damage area. The interlaminar fracture toughness of the carbon/epoxy composites was measured using a mode I test. The critical energy release rates were increased by 77% compared to the virgin carbon/epoxy composites. The surface morphology of the fractured surface was observed. The toughening mechanism of the carbon/epoxy composites was suggested based on the confirmed experimental data.

scholarly journals pH-controlled synthesis of sustainable lauric acid/SiO2 phase change material for scalable thermal energy storage

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shafiq Ishak ◽  
Soumen Mandal ◽  
Han-Seung Lee ◽  
Jitendra Kumar Singh
Keyword(s):  
Electron Microscopy ◽  
Phase Change ◽  
Lauric Acid ◽  
Photoelectron Spectroscopy ◽  
Phase Change Materials ◽  
Precursor Solution ◽  
Thermal Reliability ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Heating And Cooling

AbstractLauric acid (LA) has been recommended as economic, eco-friendly, and commercially viable materials to be used as phase change materials (PCMs). Nevertheless, there is lack of optimized parameters to produce microencapsulated PCMs with good performance. In this study, different amounts of LA have been chosen as core materials while tetraethyl orthosilicate (TEOS) as the precursor solution to form silicon dioxide (SiO2) shell. The pH of precursor solution was kept at 2.5 for all composition of microencapsulated LA. The synthesized microencapsulated LA/SiO2 has been characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), X-Ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM). The SEM and TEM confirm the microencapsulation of LA with SiO2. Thermogravimetric analysis (TGA) revealed better thermal stability of microencapsulated LA/SiO2 compared to pure LA. PCM with 50% LA i.e. LAPC-6 exhibited the highest encapsulation efficiency (96.50%) and encapsulation ratio (96.15%) through Differential scanning calorimetry (DSC) as well as good thermal reliability even after 30th cycle of heating and cooling process.

scholarly journals Effect of DMPA and Molecular Weight of Polyethylene Glycol on Water-Soluble Polyurethane

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1915 ◽  
Author(s):  
Eyob Wondu ◽  
Hyun Woo Oh ◽  
Jooheon Kim
Keyword(s):  
Molecular Weight ◽  
Contact Angle ◽  
Polyethylene Glycol ◽  
Photoelectron Spectroscopy ◽  
Water Solubility ◽  
Soft Segment ◽  
Water Soluble ◽  
Size Exclusion ◽  
Resonance Spectroscopy ◽  
Scanning Calorimetry

In this study water-soluble polyurethane (WSPU) was synthesized from isophorone diisocyanate (IPDI), and polyethylene glycol (PEG), 2-bis(hydroxymethyl) propionic acid or dimethylolpropionic acid (DMPA), butane-1,4-diol (BD), and triethylamine (TEA) using an acetone process. The water solubility was investigated by solubilizing the polymer in water and measuring the contact angle and the results indicated that water solubility and contact angle tendency were increased as the molecular weight of the soft segment decreased, the amount of emulsifier was increased, and soft segment to hard segment ratio was lower. The contact angle of samples without emulsifier was greater than 87°, while that of with emulsifier was less than 67°, indicating a shift from highly hydrophobic to hydrophilic. The WSPU was also analyzed using Fourier transform infrared spectroscopy (FT-IR) to identify the absorption of functional groups and further checked by X-ray photoelectron spectroscopy (XPS). The molecular weight of WSPU was measured using size-exclusion chromatography (SEC). The structure of the WSPU was confirmed by nuclear magnetic resonance spectroscopy (NMR). The thermal properties of WSPU were analyzed using thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC).

New Fe-Ni Based Metal-Metalloid Glassy Alloys Prepared by Mechanical Alloying and Rapid Solidification

1996 ◽  
Vol 455 ◽  
Author(s):  
J. J. Suñol ◽  
M. T. Clavaguera-Mora ◽  
N. Clavaguera ◽  
T. Pradell
Keyword(s):  
Mechanical Alloying ◽  
Rapid Solidification ◽  
Melt Spinning ◽  
Magnetic Interaction ◽  
Processing Route ◽  
Mechanically Alloyed ◽  
Scanning Calorimetry ◽  
Glassy Alloys ◽  
Rapidly Solidified ◽  
Thermal Stability Of

ABSTRACTMechanical alloying and rapid solidification are two important routes to obtain glassy alloys. New Fe-Ni based metal-metalloid (P-Si) alloys prepared by these two different processing routes were studied by differential scanning calorimetry and transmission Mössbauer spectroscopy. Mechanical alloyed samples were prepared with elemental precursors, and different nominal compositions. Rapidly solidified alloys were obtained by melt-spinning. The structural analyses show that, independent of the composition, the materials obtained by mechanical alloying are not completely disordered whereas fully amorphous alloys were obtained by rapid solidification. Consequently, the thermal stability of mechanically alloyed samples is lower than that of the analogous material prepared by rapid solidification. The P/Si ratio controls the magnetic interaction of the glassy ribbons obtained by rapid solidification. The experimental results are discussed in terms of the degree of amorphization and crystallization versus processing route and P/Si ratio content.

Preparation and Characterization of Chitosan-Casein Phosphopeptides Biocomposite Coatings on the Medical Titanium Alloy

2011 ◽  
Vol 480-481 ◽  
pp. 1065-1069
Author(s):  
Bin Liu ◽  
Lin Wang ◽  
Yin Zhong Bu ◽  
Sheng Rong Yang ◽  
Jin Qing Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Attenuated Total Reflectance ◽  
Ti Alloy ◽  
Force Microscopy ◽  
Implant Materials ◽  
Atomic Force ◽  
Casein Phosphopeptides ◽  
Potential Applications ◽  
First Time

Titanium (Ti) and its alloys have been applied in orthopedics as one of the most popular biomedical metallic implant materials. In this work, to enhance the bioactivity, the surface of Ti alloy pre-modified by silane coupling agent and glutaraldehyde was covalently grafted with chitosan (CS) via biochemical multistep self-assembled method. Then, for the first time, the achieved surface was further immobilized with casein phosphopeptides (CPP), which are one group of bioactive peptides released from caseins in the digestive tract and can facilitate the calcium adsorption and usage, to form CS-CPP biocomposite coatings. The structure and composition of the fabricated coatings were characterized by X-ray photoelectron spectroscopy (XPS), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and atomic force microscopy (AFM). As the experimental results indicated, multi-step assembly was successfully performed, and the CS and CPP were assembled onto the Ti alloy surface orderly. It is anticipated that the Ti alloys modified by CS-CPP biocomposite coatings will find potential applications as implant materials in biomedical fields.

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