scholarly journals Preparation of MgO-Templated N-Doped Mesoporous Carbons from Polyvinylpyrrolidone: Effect of Heating Temperature on Pore Size Distribution

2019 ◽  
Vol 5 (2) ◽  
pp. 15
Author(s):  
Tomoya Takada ◽  
Mayu Kurihara

Magnesium oxide (MgO)-templated nitrogen (N)-doped mesoporous carbons were prepared by using polyvinylpyrrolidone (PVP) as a raw material and magnesium lactate (Mglac) as a precursor for the MgO template to examine the influence of heating temperature and MgO precursor (magnesium acetate was used in similar previous studies) on the pore size and nitrogen content. The MgO-templated carbon was obtained by heating the PVP/Mglac mixture in an inert atmosphere followed by an acid treatment for MgO removal. The mesopore size of the carbons was approximately 4 nm regardless of heating temperature, corresponding to the crystallite size of the MgO template estimated via X-ray diffraction. This indicates that the mesopore of approximately 4 nm was generated using the MgO template. However, larger pores were also found to exist. This result indicates that the larger pores generated through processes other than the MgO templating, likely the thermal decomposition of PVP, are contained in the templated carbon. The volume of the larger pores and the specific surface area increased with increasing heating temperature. The nitrogen content of the carbon decreased as the heating temperature was increased, but it was found to be irrelevant to the MgO precursor.

Processes ◽  
2019 ◽  
Vol 7 (1) ◽  
pp. 47 ◽  
Author(s):  
Yunbing Hou ◽  
Pengchu Ding ◽  
Dong Han ◽  
Xing Zhang ◽  
Shuxiong Cao

Blast furnace slag (BFS) is often used as a cement-based raw material for underground filling and surface cemented paste discharge of tailings during mining processes. This paper studied a new cement-based material (NCM) with BFS to replace ordinary Portland cement (OPC). A uniaxial compressive strength (UCS) experiment was used to test the mechanical strength of samples; X-ray diffraction and thermal gravity experiments were used to test the crystalline phases and amount of hydration products by samples; a scanning electron microscope experiment was used to observe the influence of the hydration products morphology by samples; mercury intrusion porosimetry experiment was used to analyze the pore size distribution of samples. The samples with NCM had an optimum UCS; the crystalline phases of the hydration products were similar in OPC and NCM. However, the amount of product formed in OPC was less than that in NCM at the same curing time; more ettringite and calcium silicate hydrate were produced in samples with NCM, which filled the pores and enhanced the UCS of the samples. The final mercury intrusion volume of the samples with NCM were lower than the samples with OPC at the same curing time, which showed that samples with NCM had lower porosities. For the samples with NCM and OPC cured from 7 days to 28 days, the mercury intrusion volume was reduced by 18% and 13%, and the most common pore size of the samples reduced by 53% and 29%, respectively. This showed after 21 days curing time, the pores of all the samples getting smaller; however, the samples with NCM were more compact. The main ingredients of the NCM were clinker, lime, gypsum and BFS, and its ratio was 14:6:10:70. The content of additives to NCM was 0.4%, and the ratio of sodium sulfate: alum: sodium fluorosilicate was 2:1:1.


2019 ◽  
Author(s):  
KAIKAI MA ◽  
Peng Li ◽  
John Xin ◽  
Yongwei Chen ◽  
Zhijie Chen ◽  
...  

Creating crystalline porous materials with large pores is typically challenging due to undesired interpen-etration, staggered stacking, or weakened framework stability. Here, we report a pore size expansion strategy by self-recognizing π-π stacking interactions in a series of two-dimensional (2D) hydrogen–bonded organic frameworks (HOFs), HOF-10x (x=0,1,2), self-assembled from pyrene-based tectons with systematic elongation of π-conjugated molecular arms. This strategy successfully avoids interpene-tration or staggered stacking and expands the pore size of HOF materials to access mesoporous HOF-102, which features a surface area of ~ 2,500 m2/g and the largest pore volume (1.3 cm3/g) to date among all reported HOFs. More importantly, HOF-102 shows significantly enhanced thermal and chemical stability as evidenced by powder x-ray diffraction and N2 isotherms after treatments in chal-lenging conditions. Such stability enables the adsorption of dyes and cytochrome c from aqueous media by HOF-102 and affords a processible HOF-102/fiber composite for the efficient photochemical detox-ification of a mustard gas simulant.


2020 ◽  
Vol 849 ◽  
pp. 113-118
Author(s):  
Yayat Iman Supriyatna ◽  
Slamet Sumardi ◽  
Widi Astuti ◽  
Athessia N. Nainggolan ◽  
Ajeng W. Ismail ◽  
...  

The purpose of this study is to characterize Lampung iron sand and to conduct preliminary experiments on the TiO2 synthesis which can be used for the manufacturing of functional food packaging. The iron sand from South Lampung Regency, Lampung Province that will be utilized as raw material. The experiment was initiated by sieving the iron sand on 80, 100, 150, 200 and 325 mesh sieves. Analysis using X-Ray Fluorescence (XRF) to determine the element content and X-Ray Diffraction (XRD) to observe the mineralization of the iron sand was conducted. The experiment was carried out through the stages of leaching, precipitation, and calcination. Roasting was applied firstly by putting the iron sand into the muffle furnace for 5 hours at a temperature of 700°C. Followed by leaching using HCl for 48 hours and heated at 105°C with a stirring speed of 300 rpm. The leaching solution was filtered with filtrate and solid residue as products. The solid residue was then leached using 10% H2O2 solution. The leached filtrate was heated at 105°C for 40 minutes resulting TiO2 precipitates (powder). Further, the powder was calcined and characterized. Characterization of raw material using XRF shows the major elements of Fe, Ti, Mg, Si, Al and Ca. The highest Ti content is found in mesh 200 with 9.6%, while iron content is about 80.7%. While from the XRD analysis, it shows five mineral types namely magnetite (Fe3O4), Rhodonite (Mn, Fe, Mg, Ca) SiO3, Quart (SiO2), Ilmenite (FeOTiO2) and Rutile (TiO2). The preliminary experiment showed that the Ti content in the synthesized TiO2 powder is 21.2%. The purity of TiO2 is low due to the presence of Fe metal which is dissolved during leaching, so that prior to precipitation purification is needed to remove impurities such as iron and other metals.


Author(s):  
F. Mostefa ◽  
Nasr Eddine Bouhamou ◽  
H.A. Mesbah ◽  
Salima Aggoun ◽  
D. Mekhatria

This work aims to study the feasibility of making a geopolymer cement based on dredged sediments, from the Fergoug dam (Algeria) and to evaluate their construction potential particularly interesting in the field of special cementitious materials. These sediments due to their mineralogical composition as aluminosilicates; are materials that can be used after heat treatment. Sedimentary clays were characterized before and after calcination by X-ray diffraction, ATG / ATD, spectroscopy (FTIR) and XRF analysis. The calcination was carried out on the raw material sieved at 80 μm for a temperature of 750 ° C, for 3.4 and 5 hours. The reactivity of the calcined products was measured using isothermal calorimetric analysis (DSC) on pastes prepared by mixing an alkaline solution of sodium hydroxide (NaOH) 8 M in an amount allowing to have a Na / Al ratio close to 1 (1: 1). Also, cubic mortar samples were prepared with a ratio L / S: 0.8, sealed and cured for 24 hours at 60 ° C and then at room temperature until the day they were submited to mechanical testing. to check the extent of geopolymerization. The results obtained allowed to optimize the calcination time of 5 hours for a better reactivity of these sediments, and a concentration of 8M of sodium hydroxide and more suitable to have the best mechanical performances.


2012 ◽  
Vol 620 ◽  
pp. 314-319
Author(s):  
Nur Amira Mamat Razali ◽  
Fauziah Abdul Aziz ◽  
Saadah Abdul Rahman

Hardwood is wood from angiosperm trees. The characteristic of hardwood include flowers, endosperm within seeds and the production of fruits that contain the seeds. This paper aims to discuss the preparation and characterization of cellulose obtained from hardwood. The hardwood Merbau (Intsia bijuga) was chosen as raw material in this study. Alkaline treatment and delignification methods were used for the preparation of cellulose. Acid hydrolysis was employed to produce cellulose nanocrystal (CNC). The treated and untreated samples were characterized using x-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). The final product, from both trated and untreated samples were then compared.


2012 ◽  
Vol 454 ◽  
pp. 324-328
Author(s):  
Yan He ◽  
Ya Jing Liu ◽  
Yong Lin Cao ◽  
Li Xia Zhou

Infra-red absorption spectrometry, X-ray diffraction observations and characterization tests based on silicon molybdenum colorimetric method were used to investigate the optimal pH value controlling the stability of the silicic acid form. The experiment process was done by using sodium silicate as raw material. The results showed that the solution of silicate influenced the polymerization. The active silicic acid solution with a certain degree of polymerization was obtained by controlling the pH values.


2012 ◽  
Vol 620 ◽  
pp. 384-388
Author(s):  
Sharifah Aishah Syed Salim ◽  
Julie Juliewatty Mohamed ◽  
Zainal Arifin Ahmad ◽  
Zainal Arifin Ahmad

Numerous methods have been used to produce high purity TiC. There is no previous study has been reported on the formation using single elemental powders of Titanium (Ti) and Carbon (C) with addition Nickel (Ni) by tungsten inert gas (TIG) weld method. In this work, TiC was synthesized via TIG method by arc melting elemental powder mixture of Ti and C at ~5 second (s) and 80 ampere (A). The effect Ni contents on TiC formation was investigated. The mixed raw material was ball milled for 24 hours followed by synthesis via TIG method. The arced samples were characterized by X-ray diffraction (XRD) and Scanning electron microscope (SEM). It was revealed, that small amount of Ni additive to the metal powder allows the production of dense and tough TiC.


2018 ◽  
Vol 2017 (1) ◽  
pp. 219-228
Author(s):  
Fengling Liu ◽  
Ziyan Guo ◽  
Hui Qiu ◽  
Xia Lu ◽  
Hua Fang ◽  
...  

Abstract Four kinds of mesoporous carbons, C1-h-w, C2-h-h, C3-s-w, and C4-s-h, with different pore geometries were prepared and characterised, and their adsorption behaviours with aqueous direct yellow 12 (DY-12) were investigated. The results of X-ray diffraction and transmission electron microscopy show that C1-h-w and C3-s-w have wormlike pore characteristics, whereas C2-h-h and C4-s-h have 2-D hexagonally arranged pores. According to the N2 adsorption/desorption results, the specific surface area of C1-h-w (1,378 m2/g) is the largest among the four carbons. The adsorption isotherms could be effectively fitted using the Langmuir model. The maximum adsorption amounts of C1-h-w, C2-h-h, C3-s-w and C4-s-h are 0.968 mmol/g, 0.726 mmol/g, 0.161 mmol/g and 0.156 mmol/g, respectively. The pseudo-second-order rate constants of C1-h-w (39.8 g/(mmol·min)) and C2-h-h (7.28 g/(mmol·min)) are substantially larger than those of C3-s-w (0.0046 g/(mmol·min)) and C4-s-h (0.014 g/(mmol·min)), indicating that an open and interconnected pore geometry is favourable for DY-12 adsorption. Furthermore, DY-12 diffusion in 2-D hexagonally ordered cylindrical pores is superior to that in wormlike pores due to the smoothness of the channels in the former. External mass transfer and intraparticle diffusion both play roles in the adsorption process.


2014 ◽  
Vol 1056 ◽  
pp. 12-15 ◽  
Author(s):  
Wen Long Zhang ◽  
Wen Long Zhao ◽  
Ya Jie Dai

Reed Pulp was Raw Material that Pretreated by Four Methods {ultrasonic, Microwave, N, N-Dimethyl Acetamide (DMAc) and Tetrahydrofuran (THF)}. Reed Microcrystalline Cellulose (MCC) was Prepared by the Dilute Hydrochloric Acid Hydrolysis from Pretreated Reed Pulp. the Influences of Pretreatment Methods on Crystalline Type, Crystallinity and Crystallite Size of MCC were Investigated by X-Ray Diffraction (XRD). the Results Showed that the Crystallinity of MCC with Four Pretreatment Methods was 68.45%, 62.28%, 63.21% and 69.56%, Respectively. the Average Crystallite Size of MCC Prepared by Hydrolysis after Pretreated by Dmac was the Largest. whereas, the Crystal Type of MCC was Not Changed, it was still the Cellulose Type I. Comprehensive Analysis Indicated that the Effects of MCC Prepared by Hydrolysis after Pretreated by Ultrasonic were the Best.


Minerals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 819
Author(s):  
Pura Alfonso ◽  
Oriol Tomasa ◽  
Luis Miguel Domenech ◽  
Maite Garcia-Valles ◽  
Salvador Martinez ◽  
...  

Tailings from the Osor fluorite mines release large amounts of potentially toxic elements into the environment. This work is a proposal to remove these waste materials and use them as a raw material in the manufacture of glass. The chemical composition of the tailings was determined by X-ray fluorescence and the mineralogy by X-ray diffraction. Waste materials have SiO2, Al2O3 and CaO contents suitable for a glass production, but Na as NaCO3 has to be added. Two glass formulations, with 80–90% of the residue and 10–20% Na2CO3, have been produced. The crystallization temperatures, obtained by differential thermal analysis, were 875 and 901 °C, and the melting temperatures were 1220 and 1215 °C for the G80-20 and G90-10 glasses, respectively. The transition temperatures of glass were 637 and 628 °C. The crystalline phases formed in the thermal treatment to produce devitrification were nepheline, plagioclase and diopside in the G80-20 glass, and plagioclase and akermanite-gehlenite in the G90-10 glass. The temperatures for the fixed viscosity points, the working temperatures and the coefficient of expansion were obtained. The chemical stability of the glass was tested and results indicate that the potentially toxic elements of the tailings were incorporated into the glass structure.


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