scholarly journals Polyurethane Composite Foams Synthesized Using Bio-Polyols and Cellulose Filler

Materials ◽  
2021 ◽  
Vol 14 (13) ◽  
pp. 3474
Author(s):  
Katarzyna Uram ◽  
Milena Leszczyńska ◽  
Aleksander Prociak ◽  
Anna Czajka ◽  
Michał Gloc ◽  
...  
Keyword(s):  
Cross Sections ◽  
Raw Materials ◽  
Polyurethane Foams ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
Polyurethane Composite ◽  
Composite Foams ◽  
Closed Cell ◽  
Ft Ir ◽  
The Fourier Transform

Rigid polyurethane foams were obtained using two types of renewable raw materials: bio-polyols and a cellulose filler (ARBOCEL® P 4000 X, JRS Rettenmaier, Rosenberg, Germany). A polyurethane system containing 40 wt.% of rapeseed oil-based polyols was modified with the cellulose filler in amounts of 1, 2, and 3 php (per hundred polyols). The cellulose was incorporated into the polyol premix as filler dispersion in a petrochemical polyol made using calenders. The cellulose filler was examined in terms of the degree of crystallinity using the powder X-ray diffraction PXRD -and the presence of bonds by means of the fourier transform infrared spectroscopy FT-IR. It was found that the addition of the cellulose filler increased the number of cells in the foams in both cross-sections—parallel and perpendicular to the direction of the foam growth—while reducing the sizes of those cells. Additionally, the foams had closed cell contents of more than 90% and initial thermal conductivity coefficients of 24.8 mW/m∙K. The insulation materials were dimensionally stable, especially at temperatures close to 0 °C, which qualifies them for use as insulation at low temperatures.

scholarly journals Synthesis, Characterization and Mechanical Properties of Novel Bio-Based Polyurethane Foams Using Cellulose-Derived Polyol for Chain Extension and Cellulose Citrate as a Thickener Additive

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2802
Author(s):  
Loredana Maiuolo ◽  
Fabrizio Olivito ◽  
Vincenzo Algieri ◽  
Paola Costanzo ◽  
Antonio Jiritano ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Mechanical Tests ◽  
Reduction Reaction ◽  
Polyurethane Foams ◽  
Chain Extension ◽  
Polyurethane Composite ◽  
Composite Foams ◽  
Bio Oil ◽  
Ft Ir ◽  
Flexible Polyurethane

A novel series of bio-based polyurethane composite foams was prepared, employing a cellulose-derived polyol for chain extension and cellulose-citrate as a thickener additive. The utilized polyol was obtained from the reduction reaction of cellulose-derived bio-oil through the use of sodium borohydride and iodine. Primarily, we produced both rigid and flexible polyurethane foams through chain extension of the prepolymers. Secondly, we investigated the role of cellulose citrate as a polyurethane additive to improve the mechanical properties of the realized composite materials. The products were characterized by FT-IR spectroscopy and their morphologies were analysed by SEM. Mechanical tests were evaluated to open new perspectives towards different applications.

Improvement of thermal conductivity of rigid polyurethane foams with aluminum nitride filler

2021 ◽  
pp. 026248932198897
Author(s):  
Serife Akkoyun ◽  
Meral Akkoyun
Keyword(s):  
Thermal Conductivity ◽  
Aluminum Nitride ◽  
Polyurethane Foams ◽  
Thermal Transitions ◽  
Rigid Polyurethane Foams ◽  
Noticeable Increase ◽  
Polyurethane Composite ◽  
Composite Foams ◽  
Step Procedure ◽  
Electrical Conductivities

The aim of this work is the fabrication of electrically insulating composite rigid polyurethane foams with improved thermal conductivity. Therefore, this study is focused on the effect of aluminum nitride (AlN) on the thermal and electrical conductivities of rigid polyurethane foams. For this purpose, aluminum nitride/rigid polyurethane composite foams were prepared using a three-step procedure. The electrical and thermal conductivities of the foams were characterized. The thermal transitions, mechanical properties and morphology of the foams were also examined. The results reveal that AlN induces an increase of the thermal conductivity of rigid polyurethane foam of 24% which seems to be a relatively noticeable increase in polymeric foams. The low electrical conductivity of the foams is preserved.

Study on Modified Rapeseed Oil/Montmorillonite Nanocomposites

2010 ◽  
Vol 123-125 ◽  
pp. 1291-1294 ◽  
Author(s):  
Bin Lü ◽  
Jian Zhong Ma ◽  
Dang Ge Gao ◽  
Lei Hong
Keyword(s):  
Rapeseed Oil ◽  
Fourier Transforms ◽  
Raw Materials ◽  
Infrared Spectrometry ◽  
Emulsifying Properties ◽  
X Ray Diffraction ◽  
Layer Spacing ◽  
Transmission Electron ◽  
Ft Ir ◽  
Better Than

Modified rapeseed oil(MRO) was prepared by using rapeseed oil, ethylene diamine and acrylic acid as the raw materials. Modified rapeseed oil/montmorillonite(MRO/MMT) nanocomposite was prepared by using modified rapeseed oil and montmorillonite. The emulsifying properties of MRO and MRO/MMT were determined respectively. Fourier transforms infrared spectrometry (FT-IR) and Transmission Electron microscope (TEM) results showed that MRO/MMT was prepared successfully. X-ray diffraction (XRD) results showed that modified rapeseed oil could smoothly enter the interlayer of montmorillonite, and modified the montmorillonite; with an increase in the amount of montmorillonite, the layer spacing of montmorillonite in the MRO/MMT lower after the first increase. The results of emulsifying properties indicated that emulsifying properties of MRO/MMT was better than MRO.

Preparation and Photocatalytic Activity of Cu/BiVO4 by Solid State Grinding Method for Degradation of Methyl Orange

2016 ◽  
Vol 703 ◽  
pp. 321-325
Author(s):  
Hai Feng Chen ◽  
Jia Mei Chen ◽  
Zhi Xue Pan
Keyword(s):  
Methyl Orange ◽  
Solid State ◽  
Visible Light ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
Illumination Time ◽  
Grinding Method ◽  
Ft Ir ◽  
Degradation Of Methyl Orange

In this work, novel Cu/BiVO4 photocatalyst were prepared by a low-temperature solid state grinding method using Bi (NO3)3•5H2O, NH4VO3 and Cu (NO3)2•2H2O as raw materials. The structure and properties of the samples were characterized by Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD) and UV-vis diffused reflectance spectroscopy (DRS); Using the degradation of methyl orange (MO) as the probe, it was simulated as the degradation of sewage under the visible light to study the influence of the illumination time and the amount of photocatalysts. Compared with the pure BiVO4, the visible-light absorption scope of BiVO4 was broadened by doping Cu, the UV-Visible absorption edges were slightly red shift and the band gap was narrower. Comparatively speaking, the results indicted that the doped Cu enhanced the photocatalytic activities of BiVO4.

Preparation of Lithium Niobate Powders by Mechanochemical Process

2011 ◽  
Vol 121-126 ◽  
pp. 3401-3405 ◽  
Author(s):  
Ju Hua Luo
Keyword(s):  
Lithium Niobate ◽  
Raw Materials ◽  
High Energy ◽  
Energy Reduction ◽  
X Ray Diffraction ◽  
Direct Formation ◽  
Ft Ir ◽  
Energy Ball ◽  
Mechanochemical Treatments ◽  
Mixture Samples

Lithium niobate powders were prepared by mechanochemical treatments using Li2CO3 and Nb2O5 as raw materials. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) were employed to evaluate the morphologies and structures of samples. The mechanism of LiNbO3 formation of the ground mixture samples was discussed. The crystal structure of mixture was collapsed into a disordered structure, which increased with increasing grinding time. At the same time, the specific surface area increase and the bond energy reduction of the mixture occurred. Consequently, high energy ball milling enables increase of the internal energy, reduction of the activation energy, and improvement of the uniform mixing stage, which resulted in direct formation of singal phase LiNbO3 at a low temperature (500°C). However, the temperature must reach 1200°C for the traditional method.

Preparation of Manganese Ferrite Powders by Mechanochemical Process

2011 ◽  
Vol 284-286 ◽  
pp. 2268-2271 ◽  
Author(s):  
Ju Hua Luo
Keyword(s):  
Single Phase ◽  
Raw Materials ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
Mechanochemical Method ◽  
X Ray ◽  
Starting Mixture ◽  
Ft Ir ◽  
Mechanochemical Treatments ◽  
Firing Method

Mn-ferrite powders were prepared by mechanochemical treatments using MnO2and Fe2O3as raw materials. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometry (VSM) were employed to evaluated the morphologies and structures of samples. The results indicated that the starting mixture became amorphous stage after ball-milled for 40h, and single phase MnFe2O4could be obtained after annealed at 1200°C for 2h. In comparison with the traditional firing method , the mechanochemical method benefited achieving the higher saturation magnetization, which indicated that the samples had a better magnetic properties.

Preparation and Properties Study on the Composites of Polypropylene and Polyphenylene Sulfide Filled by Modified Molybdenum Disulfide

2009 ◽  
Vol 87-88 ◽  
pp. 345-350
Author(s):  
Jian Qiang Zhang ◽  
Hui Xia Feng ◽  
Jian Hui Qiu
Keyword(s):  
Surface Modification ◽  
Molybdenum Disulfide ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Polyphenylene Sulfide ◽  
X Ray Diffraction ◽  
Infrared Spectrometer ◽  
Ft Ir ◽  
The Fourier Transform ◽  
Wear Modes

The wet surface modification process were used in this work to get the well lipophilic molybdenum disulfide (MoS2) powders and the modified MoS2 were filled into the polyphenylene sulfide (PPS) and polypropylene (PP) powders with different proportions to make polymeric based composites through hot-press molding equipment. The Fourier transform infrared spectrometer (FT-IR) analysis showed that the modification agents of stearic acid (SA), orγ-Methacryloxypropyl trimethoxy silane(KH570 or A-174), could react with the adsorption hydroxyl(−OH) of the MoS2 powders and finally form chemical coatings, the SA could form a layer of physics wrap too. The powder X-ray diffraction (XRD) analysis reveled that the SA or KH570 could not change the laminated structure of MoS2. The wearability testing showed that the composites filled by modified MoS2 owned the better wearable performances than the filled not one. From minimum to maximum, the wear mass rates of SA/MoS2/PP/PPS, KH570/MoS2/PP/PPS, PP/PPS were 0.7216, 5.4187 and 7.3198 percent in turns. Scanning electronic microscope (SEM) analysis showed the surface modification could uniformize the modified MoS2 to disperse in the polymeric based composites, and also reflect the abrasion mechanism which the particles and the adhering wear modes could all make the mass loss of the testing samples and they coexisted and could transform each other, the former would produce higher loss rates than the later and their leader status would gradually change from the particles wear to the adhering wear during the course of wearing-resisting tests.

Synthesis of V2O5 Powders by EDTA Assistance Ultrasound Sol-Gel Process

2012 ◽  
Vol 512-515 ◽  
pp. 207-210
Author(s):  
Quan Wen ◽  
Jian Feng Huang ◽  
Li Yun Cao ◽  
Jian Peng Wu
Keyword(s):  
Activation Energy ◽  
Raw Materials ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Calcination Temperatures ◽  
Sol Gel Process ◽  
Ft Ir ◽  
Precursor Powders ◽  
Influence Of Ph

V2O5 powders were successfully synthesized by the EDTA assistanced ultrasound sol-gel process using NH4VO3 and EDTA, NH3•H2O as raw materials. The synthesized activation energy and the influence of pH values and the calcination temperatures on the phases and microstructures of powders were particularly investigated. The precursor powders and the V2O5 powders were characterized by X-ray diffraction (XRD), fourier transform inelectron microscopy (FT-IR), scanning electron microscopy (SEM) and differential scanning calorimetry-thermal gravimetric (DSC-TG). Results show that the obtained products exhibit good crystallization under the conditions of pH=4, calcination temperature 400~500 °C and calcination time 0.5 h during the synthesizing process. The as-prepared V2O5 powders show preferred growth orientation along (001) plane at the pH=4. By DSC analysis, the ultrasonic cavitation result in the decrease in synthesized activation energy obviously than that was prepared without ultrasonic irradiation.

Synthesis and Magnetic Properties of La-Doped Ni Ferrites

2010 ◽  
Vol 148-149 ◽  
pp. 736-739
Author(s):  
Ju Hua Luo
Keyword(s):  
Single Phase ◽  
Raw Materials ◽  
Nominal Composition ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Magnetic Parameters ◽  
Ft Ir ◽  
Mechanochemical Treatments ◽  
La Doped

Ni ferrites doped with lanthanum with a nominal composition of NiFe2-xLaxO4(x=0.05) were obtained by mechanochemical treatments using NiCO3•2Ni (OH)2•4H2O , La2O3 and Fe2O3 as raw materials. Both series of materials were characterised by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometry (VSM). The results indicated that the mixture became amorphous stage after ball-milled for 30 h, and single phase NiFe1.95La0.05O4 could be obtained after calcined at 700 for 2 h. The addition of lanthanum resulted in a reduction of all the magnetic parameters evaluated.

The Synthesis and Crystallization of Poly(vinylidene fluoride) in Supercritical CO2

e-Polymers ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Zhendong Shi ◽  
Zhen Zheng ◽  
Xiaoli Su ◽  
Xinling Wang
Keyword(s):  
Vinylidene Fluoride ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Molecular Weights ◽  
Good Solubility ◽  
Poly Vinylidene Fluoride ◽  
Ft Ir ◽  
Application Fields ◽  
Crystallization Mode

AbstractA series of poly(vinylidene fluoride)s (PVDFs) is synthesized in supercritical carbon dioxide (sc-CO2). The influences of polymerization pressure, molecular weight distribution and H-H defect concentration on the crystallization of PVDF have been studied in combination with differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXRD) and Fourier transform infrared spectroscopy (FT-IR) measurements. The result shows that the morphology, molecular weights, polydispersity and head-to-head (H-H) defect concentrations of the PVDFs are affected by the reaction pressure and good solubility generated from sc-CO2. Especially, the sc-CO2 polymerization has greatly improved the crystallization mode of the obtained PVDFs such as the complete degree of crystallinity, crystallinity and the crystal phase. This will create more comprehensive application fields for PVDF.

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