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.

scholarly journals Preparation of aluminum-ferric-magnesium polysilicate and its application on oily sludge

2015 ◽  
Vol 80 (12) ◽  
pp. 1553-1565 ◽  
Author(s):  
Si Li ◽  
Shuang Yang ◽  
Pan Yi ◽  
Jin-Hui Zhang
Keyword(s):  
Removal Efficiency ◽  
Ph Value ◽  
Xrd Analysis ◽  
Oily Sludge ◽  
X Ray Diffraction ◽  
Chemical Structures ◽  
Coagulation Performance ◽  
Ft Ir ◽  
Oily Water ◽  
The Fourier Transform

Aluminum-ferric-magnesium polysilicate (PAFMS) was prepared by introducing aluminum, ferric and magnesium metal ions into Polymer silica acid solution. PAFMS was applied in the treatment of oily wastewater from treatment of oily sludge in this paper, and the coagulation performance was valued by the removal efficiency of turbidity and colority. The structure and morphology of PAFMS were characterized by the Fourier Transform Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD) and Scanning Electronic Microscopy (SEM). The results indicated that mole ratios 6:4:15 of Al:Fe:Mg is beneficial to forming of Al-O-Si, Fe-O-Si and Mg-Si-O. Fe played main inhibition role among the three metals. XRD analysis showed that the addition of Al, Fe and Mg into Polysilicon acid did not produce a simple mixture, but resulted in the formation of new chemical structures. The intensity of peaks was influenced by the mole ratios of metals. SEM spectra presented that PAFMS appeared to be a spatial structure consisting of many irregular protuberant parts. The removal efficiency of turbidity and colority in oily water from the treatment of oily sludge was better when the mole ratio of (Al+Fe+Mg):Si was 0.5 and if the mole ratios of Al:Fe:Mg are kept at 6:4:15. Moreover, when the dosage of PAFMS was 1.4-1.8 % and the pH value in range of 8-9, the efficiency of turbidity and colority removal are up to 97.3 and 96.8%, respectively.

Effects of Sintering Temperature on the Phase Changes of Woodceramics Prepared from Liquefication Wood

2013 ◽  
Vol 331 ◽  
pp. 448-451
Author(s):  
De Lin Sun ◽  
Xian Chun Yu
Keyword(s):  
Sintering Temperature ◽  
Xrd Analysis ◽  
Phase Changes ◽  
X Ray Diffraction ◽  
Diffraction Angle ◽  
Graphite Structure ◽  
Ft Ir ◽  
Ir Analysis ◽  
The Fourier Transform ◽  
Degree Of Graphitization

Discarded wood was liquefied with phenol to prepare the liquefication basic woodceramics (LBW). The effects of sintering temperature on the phase changes had discussed. The Fourier transform infrared (FT-IR) analysis showed that, as sintering temperature rose, the elements of H and O were excluded gradually, as well the circle C-C structure had formed. The X-ray diffraction (XRD) analysis indicated that higher sintering temperature could improve the microcrystal structure. With the temperature increasing, (002) diffraction peak became strong and the diffraction angle 2θbecame larger, meanwhile, the stacking height of larger plane and the crystallite size increased also. In addition, the distances of interlamination drop drown, and the rank of microcrystal became more regulation and order. Butgvalues which character the degree of graphitization always were less than zero, and the integrated graphite structure had not found, suggesting the LBW was a kind of a difficult graphitization material.

scholarly journals Production and Characterization of Activated Carbon from Baobab Fruit Shells by Chemical Activation Using ZnCl2, H3PO4 and KOH

2021 ◽  
Vol 2129 (1) ◽  
pp. 012009
Author(s):  
R Nedjai ◽  
N A Kabbashi ◽  
M Z Alam ◽  
M F R Al-Khatib
Keyword(s):  
Activated Carbon ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Xrd Analysis ◽  
Surface Characteristic ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
Ft Ir ◽  
Characterization Of Activated Carbon

Abstract Chemical agents have a good influence on the formation of activated carbons, surface characteristic, and its adsorption properties. In this study, the effect of activating agents (ZnCl2, KOH, and H3PO4) on baobab fruit shell (BFS) were evaluated. The characteristics of the baobab fruit shell based activated carbon (BF-ACs) were evaluated through the yield and iodine number. BF-ACs were also characterized by Scanning Electron Microscope (SEM), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray Diffraction (XRD), and nitrogen (N2) adsorption. SEM analysis illustrates those porous structures formed on the surface of BF-ACs were with different sizes. The XRD analysis show that the main structures of BF-ACs are amorphous. FT-IR data demonstrates the presence of different surface groups on the produced BF-ACs. Among activating agent, the KOH was observed to the most appropriate for the production of activated carbon with a large surface area (1029.44 m2/g) from baobab fruit shell.

Production of Micro Crystalline Cellulose from Tapioca Solid Waste: Effect of Acid Concentration on its Physico-chemical Properties

2020 ◽  
Vol 23 (5) ◽  
pp. 147-151
Author(s):  
Ansharullah Ansharullah ◽  
Nur Muhammad Abdillah Saenuddin ◽  
RH Fitri Faradilla ◽  
Asranuddin Asranudin ◽  
Asniar Asniar ◽  
...  
Keyword(s):  
Solid Waste ◽  
Water Solubility ◽  
Chemical Properties ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Crystalline Cellulose ◽  
Cellulose Content ◽  
X Ray Diffraction ◽  
Physico Chemical ◽  
Ft Ir

This study was aimed to examine the production of microcrystalline cellulose (MCC) from tapioca solid waste (TSW), using HCl hydrolysis with various concentrations, i.e., 2 N, 2.5 N, 3 N, and 3.5 N. MCC was produced by delignifying the TSW with NaOH 20%, and bleaching with NaOCl 3.5% to produce α-cellulose, and subsequently hydrolyzing α-cellulose with three different HCl concentrations to produce MCC. The physicochemical properties of MCC were then analyzed, including Scanning Electron Micrograph (SEM), X-ray diffraction (XRD), and FTIR spectra. The results showed that hydrolysis with 2.0 N HCl resulted in a higher yield of 61.28%, α-cellulose content of 56.33%, moisture 6.25%, pH of 6.54; ash 0.23%, and water solubility 0.34%. SEM analysis showed the morphology and size of the MCC produced were like those of a commercial MCC (Avicel PH101), while the XRD analysis showed the higher concentration of HCl gave rise to an increased crystalline index. FT-IR spectrum analysis indicated that TSW, MCC produced, and commercial MCC had similar functional groups.

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.

A study on using expanded perlite with hydroxyapatite: Reinforced bio-composites

2021 ◽  
pp. 095441192199656
Author(s):  
Erdoğan Karip ◽  
Mehtap Muratoğlu
Keyword(s):  
Body Fluid ◽  
Xrd Analysis ◽  
Cold Isostatic Pressing ◽  
Expanded Perlite ◽  
X Ray Diffraction ◽  
Pressing Method ◽  
X Ray ◽  
Infra Red ◽  
Ft Ir

People are exposed to different kinds of diseases or various accidents in life. Hydroxyapatite (HA) has been widely employed for bone treatment applications. In this study, HA was extracted from sheep bones. Bio-composites were doped with 1, 5, and 10 wt.% of expanded perlite and 5 wt.% of ZrO2–MgO-P2O5. The bio-composites were prepared by the cold isostatic pressing method (250 MPa) and sintered at 900°C for 1 h. In order to evaluate the characteristics of the bio-composites, microhardness, density, X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) analyses were carried out on them. Additionally, the specimens whose characteristics were determined were kept in synthetic body fluid (SBF), and their in vitro behavior was examined. As a result, it was observed that microhardness increased as both the weight and the grain size of the expanded perlite were increased. Calcium silicate, tri-calcium phosphate, and hydroxyapatite were observed in the XRD analysis of all samples, and the formation of apatite structures was increased by addition of ZrO2–MgO–P2O5.

The Characteristic Evaluation of Hydroxyapatite Powders Synthesized from CaCO3 Refined from Oyster Shell and H3PO4

2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu
Keyword(s):  
Bone Density ◽  
Inductively Coupled Plasma ◽  
Oyster Shell ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled ◽  
Infra Red ◽  
Ft Ir

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.

Development of Ternary Concrete Utilizing Agricultural Waste Material

2022 ◽  
Author(s):  
Sunita Kumari ◽  
Dhirendra Singhal ◽  
Rinku Walia ◽  
Ajay Rathee
Keyword(s):  
Rice Husk ◽  
Rice Husk Ash ◽  
Agricultural Waste ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Concrete Mix ◽  
Maize Cob

Abstract The present project proposes to utilize rice husk and maize cob husk ash in the cement to mitigate the adverse impact of cement on environment and to enhance the disposal of waste in a sustainable manner. Ternary concrete / MR concrete was prepared by using rise husk and maize cob ash with cement. For the present project, five concrete mixes MR-0 (Control mix), MR-1 (Rice husk ash 10% and MR-2.5%), MR-2 (Rice husk ash 10% and MR-5%), MR-3 (Rice husk ash 10% and MR-2.5%), MR-4 (Rice husk ash 10% and MR-2.5%) were prepared. M35 concrete mix was designed as per IS 10262:2009 for low slump values 0-25mm. The purpose is to find the optimum replacement level of cement in M35 grade ternary concrete for I – Shaped paver blocks.In order to study the effects of these additions, micro-structural and structural properties test of concretes have been conducted. The crystalline properties of control mix and modified concrete are analyzed by Fourier Transform Infrared Spectroscope (FTIR), Scanning Electron Microscopy (SEM), and X-Ray Diffraction (XRD). The results indicated that 10% Rice husk ash and 5% maize cob ash replaced with cement produce a desirable quality of ternary concrete mix having good compressive strength. The results of SEM analysis indicated that the morphology of both concrete were different, showing porous structure at 7 days age and become unsymmetrical with the addition of ashes. After 28 day age, the control mix contained more quantity of ettringite and became denser than ternary concrete. XRD analysis revealed the presence of portlandite in large quantity in controlled mix concrete while MR concrete had the partially hydrated particle of alite.

scholarly journals Effects of Gum Arabic-Coated Magnetite Nanoparticles on the Removal of Pb Ions from Aqueous Solutions

2021 ◽  
pp. 889-896
Author(s):  
Hanan J. Mustafa ◽  
Tagreed M. Al-Saadi
Keyword(s):  
Aqueous Solutions ◽  
Crystallite Size ◽  
Magnetite Nanoparticles ◽  
Gum Arabic ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Absorption Bands ◽  
X Ray ◽  
Ft Ir ◽  
Pb Ions

To study the removal of lead (Pb) ions from aqueous solutions, novel magnetite nanoparticles (NPs) of Ni0.31Mg0.15Ag0.04Fe2.5O4 were synthesized by coprecipitation synthesis using metal sulfates, and then coated with Gum Arabic (GA). The prepared NPs were analyzed using various spectroscopic and analytical methods, such as X-Ray diffraction analysis (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive X-ray spectroscopy (EDX), Fourier Transform Infra-Red spectroscopy (FT-IR), and Atomic Absorption Spectrophotometer (AAS). By using XRD analysis, the cubic inverse spinel structure of the prepared NPs was proven, showing average values of crystallite size, lattice constant, and density of 28.57nm, 8.32582Å, and 5.2890 g/cm3, respectively. FE-SEM analysis revealed the sphere-like shape of the nanoparticles with a measured crystallite size of 25.93nm. The existence of constituent elements was evidenced by EDX. FT-IR test proved the success of the coating process of magnetite NPs by the presence of the main characteristic absorption bands of GA in the FT-IR spectrum of GA-magnetite NPs. The adsorption of Pb ions by GA- magnetite NPs was shown by AAS analysis, where the concentration of Pb ions decreased from 25ppm to 6.6ppm, reaching 1.1ppm at the time of 25min. The porosity of the NPs and the carboxyl groups in GA played an important role in the process.

scholarly journals Effect of Re and Tm-site on morphology structure and optical band gap of ReTmO3 (Re: La, Ce, Nd, Gd, Dy, Y and Tm: Fe, Cr) prepared by sol-gel method

2018 ◽  
Vol 64 (4) ◽  
pp. 381
Author(s):  
Muhammad Tufiq Jamil ◽  
Javed Ahmad ◽  
Syed Hamad Bukhari ◽  
Murtaza Saleem
Keyword(s):  
Band Gap ◽  
Sol Gel ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
X Ray ◽  
Average Grain Size ◽  
Auto Combustion ◽  
Uv Visible

Rare earth nano sized pollycrystalline orthoferrites and orthocromites ReT mO3 (Re = La, Nd, Gd, Dy, Y and T m = Fe, Cr) have been synthesized by sol-gel auto combustion citrate method. The samples have been characterized by means of X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDX), and UV-visible spectroscopy. The samples are single phase as confirmed by XRD analysis and correspond to the orthorhombic crystal symmetry with space group pbnm. Debye Scherer formula and Williamson Hall analysis have been used to calculate the average grain size which is consistent with that of determined from SEM analysis and varied between 25-75 nm. The elemental compositions of all samples have been checked by EDX analysis. Different crystallographic parameters are calculated with strong structural correlation among Re and Tm sites. The optical energy band gap has been calculated by using Tauc relation estimated to be in the range of 1.77 - 1.87 eV and 2.77 - 3.14 eV, for ReFeO3 and ReCrO3, respectively.

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