Influence of intrinsic parameters on the particle size of magnetic spinel nanoparticles synthesized by wet chemical methods

The synthesis of magnetic spinel ferrites at the nanoscale is a field of intense study, because the meso- scopic properties enable their novel applications. Spinel nanoparticles have a promising role because of their extraordinary properties compared with those of micro and macro scale particles. Several colloidal chemical synthetic procedures have been developed to produce monodisperse nanoparticles of spinel let- rites and other materials using sol-gel, co-precipitation, hydrothermal, and microemulsion techniques. To improve the synthesis method and conditions, quality and productivity of these nanoparticles, understanding the effect of extrinsic （pH, temperature, and molecular concentration） and intrinsic parameters （site preferences, latent heat, lattice parameters, electronic configuration, and bonding energy） on the particle size during synthesis is crucial. In this review, we discuss the effect of the intrinsic parameters on particle size of spinel ferrites to provide an insight to control their particle size more precisely.

Effects of Varieties and Cooking Methods on Physical and Chemical Characteristics of Cooked Rice

To analyze the effect of different lowland rice varieties and different cooking methods on physical and chemical characteristics of cooked rice. A factorial randomized block design with two factors was used and each combination of the factors was repeated three times. The first factor was rice variety（Ciherang and Ciliwung） and the second factor was the cooking method（stovetop, boiling and steaming, and rice cooker）. Results showed that Ciherang and Ciliwung varieties were classified into slender grain rice type with yellowred color. The amylose content of Ciherang was classified as moderate, while the amylose content of Ciliwung classified as low. The most abundant amino acid contained in Ciherang and Ciliwung varieties was glutamic acid. Statistical analysis showed that cooking method had significant effects on texture, lightness, chroma, hue and moisture content of cooked rice. Rice cooked with liwet method had the lowest texture value, lowest lightness value, highest chroma value, and highest moisture content.

A Pioneering Approach to the Synthesis of Silver Nanoparticles

Our research introduces a groundbreaking chemical reduction method for synthesizing silver nanoparticles, marking a significant advancement in the field. The nanoparticles were meticulously characterized using various techniques, including optical analysis, structural analysis, transmission electron microscopy (TEM), and field-emission scanning electron microscope (FESEM). This thorough process instills confidence in the accuracy of our findings. The results unveiled that the silver nanoparticles had a diameter of less than 20 nm, a finding of great importance. The absorption spectrum decreased in the peak wavelength range (405 - 394 mm) with increasing concentrations of Ag nanoparticles in the range (1 - 5%). The XRD results indicated a cubic crystal structure for silver nanoparticles with the lattice constant (a = 4.0855 Å), and Miller indices were (111), (002), (002), and (113). The simulation on the XRD pattern showed a face center cubic phase with space group Fm-3m, providing valuable insights into the structure of the nanoparticles.

Synthesis and Characterization of Y-Doped Mesoporous CeO_2 Using A Chemical Precipitation Method

Using cetyltrimethylammonium bromide （CTAB） as the template agent, cerium nitrate as the cerium resource, yttrium nitrate as the yttrium resource, and ammonium carbonate as the precipitating agent, mesoporous CeO2 powders doped with different yttrium contents were successfully synthesized using a chemical precipitation method, under an alkalescent condition. Properties of the obtained samples were characterized and analyzed with X-ray diffraction （XRD）, energy dispersive analysis of X-rays （EDAX）, transmission electron microscopy （TEM）, infrared （IR） absorbance, and the BET method. For the prepared samples with 20% （molar ratio） Y-doped content, a BET specific surface area of 106. 6 m^2 · g^- 1, with an average pore size of3~27 nm were obtained. XRD patterns showed that the doped samples were with a cubic fluorite structure. TEM micrographs revealed that the doped samples showed a spherical morphology with a diameter ranging from 20 to 30 nm and a round pore shape. IR results indicated that the Ce-O-Ce vibration intensity decreased as the Y-doped content increased. N2 adsorption-desorption isotherms showed that the samples possessed typical mesopore characteristics. The average pore size of the samples decreased alter mesoporous CeO2 was doped with yttrium, and the average pore size decreased largely as the Y-doped content increased.

Deposition of Bioactive Layer on NiTi Alloy by Chemical Treatment

A simple chemical method was developed for inducing bioactivity on NiTi alloys (50 at. pct by Ni/Ti). A layer of calcium phosphate was deposited on the surface to improve biocompatibility of the alloy. NiTi alloys were first etched in HNO3 aqueous solution, and then treated with boiling diluted NaOH solution. A rough surface was created and a thin TiO2 layer was formed on the surface. Pre-calcification was then introduced by immersing the treated NiTi alloys in supersaturated Na2HPO4 solution and supersaturated Ca(OH)2 solution in turn before calcification in simulated body fluid (SBF). A dense and uniform bonelike calcium phosphate (Ca-P) bioactive layer was formed on the surfaces of the specimen, which would improve their biocompatibility. Morphology and element analysis on NiTi surfaces during the treatments were investigated in detail by means of environment scanning electron microscopy (ESEM), energy dispersion X-ray spectroscopy (EDXS), and X-ray diffraction (XRD).

Effects of Heating Processing on Microstructure and Magnetic Properties of Mn-Zn Ferrites Prepared via Chemical Co-precipitation

The fine powders of Mn-Zn ferrites with uniform size were prepared via chemical co- precipitation method. X-ray diffraction analysis （XRD）, scanning electron microscopy （SEM）, vibrating sample magnetometer （VSM）, frequency dependence of permeability and metallographical microscope were used to investigate the crystal structure, surface topography and magnetic properties of the powders and the sintering samples. The experimental results demonstrate that the precursor powders have formed a pure phase cubic spinel MnxZn1-xfe2O4 while in the reactor and show definite magnetism, which can solve the difficult issue in washing process effectively. When calcined beneath 450 ℃, the powders have intact crystal form and the crystallite size is less than 20 nm. Comparison tests of sintering temperatures show that 1 300 ℃ is the ideal sintering temperature for Mn-Zn ferrites prepared by using the chemical co-precipitation.

Synthesis of γ-Al_2O_3 nanoparticles by chemical precipitation method

Highly pure active γ-Al2O3 nanoparticles were synthesized from aluminum nitrate and ammonium carbonate with a little surfactant by chemical precipitation method. The factors affecting the synthesis process were studied. The properties of γ-Al2O3 nanoparticles were characterized by DTA, XRD, BET, TEM, laser granularity analysis and impurity content analysis. The results show that the amorphous precursor AI（OH）3 sols are produced by using 0.1 mol/L Al（NO3）3·9H2O and 0.16 mol/L （NH4）2CO3·H2O reaction solutions, according to the volume ratio 1.33, adding 0.024%（volume fraction） surfactant PEG600, and reacting at 40℃, 1000 r/min stirring rate for 15min. Then, after stabilizing for 24 h, the precursors were extracted and filtrated by vacuum, washed thoroughly with deionized water and dehydrated ethanol, dried in vacuum at 80℃ for 8h, final calcined at 800℃ for 1h in the air, and high purity active γ-Al2O3 nanoparticles can be prepared with cubic in crystal system, OH^7-FD3M in space group, about 9 nm in crystal grain size, about 20 nm in particle size and uniform size distribution, 131.35 m^2/g in BET specific surface area, 7 - 11 nm in pore diameter, and not lower than 99.93% in purity.

Improvements of marine clay slurries using chemicale-physical combined method(CPCM)

In this paper, the effectiveness, applicability and validity of chemicalephysical combined methods（CPCMs） for treatment of marine clay （MC） slurries were evaluated. The method CPCM1 combineschemical stabilization and vacuum preloading （VP）, while CPCM2 is similar to CPCM1 but includes boththe application of surcharge and use of geo-bags to provide confinement during surcharge preloading.The key advantage of CPCM2 using geo-bags is that the surcharge can be immediately applied on thechemically stabilized slurries. Two types of geo-bags were investigated under simulated land filling anddyke conditions, respectively. The test results show that the shear strength （cu） of treated slurry byCPCM2 is generally much higher than that by CPCM1. Besides, the use of CPCM2 can significantly reducethe treatment time due to the short drainage paths created by geo-bags. Overall, CPCM2 allows fasterconsolidation and higher preloading that help to achieve higher mechanical properties of the stabilizedslurry. There are consistent relationships between cU and water content of slurries treated by CPCM2.Several important observations were also made based on comparisons of experimental data. 2015 Institute of Rock and Soil Mechanics, Chinese Academy of Sciences. Production and hosting byElsevier B.V. All rights reserved.

Chemical Analysis Method for Carbon Bearing Refractory Products——Determination of the Total Carbon by Combustion Gravimetric Method

GB/T 13245-91 1 Theme and Scope This standard specifies the method abstract, reagents, apparatus, specimen, analyzing procedure, result calculation and permissible tolerance used for determination of the total carbon with combustion gravimetric method.

Chemical Analysis Method for Magnesia and Magnesia-Alumina Refractories——Gravimetric-Molybdenum Blue Photometric Method for Determination of Silicon Dioxide Content

This standard specifies the gravimetric-molybdenum blue photometric method for determination of silicon dioxide content.

Quantum Chemical Calculation on the Structures and Electronic Properties of Phosphonate Ester as Rare Earth Extractants

Molecular mechanics, molecular dynamics and semi empirical quantum chemical method have been used to study the geometric and electronic structures of six phosphonate ester as rare earth extractants. The results show that the phosphorus atom exhibits sp 3 hybridization. The structures of the extractants are determined by the repulsion of the hydrocarbon groups. In the extractants that have two 2 ethyl hexyl groups, one 2 ethyl hexyl extends straight, and the other extends twistily. When the number of oxygen atom decreases, the negative charge of the phosphoryl oxygen atom increases, but the negative charge of oxygen atom and the positive charge of hydrogen of the hydroxyl group decreases, and the energies of highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital(LUMO) increase. The energies of the occupied frontier orbitals are close to each other.

The Preparation of Nano Silver by Chemical Reduction Method

A silver nanostructures prepared by using chemical reduction method. The silver nanoparticles were prepared with diameters of about (20 nm). Numerous techniques had been used to study the optical, structural like the UV-Vis absorption spectrometer, Ttransmission Electron Microscopy (TEM), Field-Emission Scanning Electron microscope (FESEM), and X-ray diffraction (XRD). The practical results exhibited the absorption spectrum of the prepared nanoparticles at (357 nm), it was found that there is a relationship between the positions of the optical absorption peak and the size of the silver nanoparticles. The analysis of TEM results showed the presence of nanoparticles in the range (20 nm). The analyzing of XRD results explained the crystal structure for silver nanoparticles. It is found a cubic unit cell have a lattice constants (a = 4.0855 Å), with the Miller indices were (111), (002), (002), and (113).

The Study of Alcoholysis of 1,2-Thiazetidine-l,l-dioxide with Quantum Chemical Method

The alcoholysis mechanism of 1,2-thiazetidine-1,1-dioxide with methanol, in which the relatively stable product is sulfonate ester, has been investigated by quantum chemical method. Our calculations indicate the reaction for alcoholysis of 1,2-thiazetidine-1,1-dioxide proceeds via two possible mechanisms: concerted and stepwise. In the stepwise mechanism, two possible reaction pathways can be followed while only one possible reaction pathway can be followed in the concerted mechanism.

Synthesis and electrochemical performance of a novel nano sized Sn_2SbNi composite

Chemical reduction method was employed to prepare nano-sized Sn2SbNi alloy composites used as anode material for rechargeable lithium ion batteries.This strategy was adopted to combine the virtues of both active/inactive and active/active alloys to fabricate a Sn2SbNi alloy powder with two active components and one inactive component.The two active components can realize the high capacity feature of electrode and can make the volume change of electrode take place in a stepwise manner due to the different lithiation potentials of two active components,leading to a stable cycling performance.Sn2SbNi alloy provides a reversible specific capacity over 640 mA·h/g with an excellent cyclic ability.The Sn-Sb-Ni alloy composite material shows to be a good candidate anode material for the lithium ion batteries.

Preparation of Superhydrophobic ZnO Films on Zinc Substrate by Chemical Solution Method

Superhydrophobic surface was prepared on the zinc substrate by chemical solution method via immersing clean pure zinc substrate into a water solution of zinc nitrate hexahydrate[Zn（NO3）2.6H2O] and hexamethylenete- traamine（C6H12N4） at 95 ℃ in water bath for 1.5 h, then modified with 18 alkanethiol. The best resulting surface shows superhydrophobic properties with a water contact angle of about 158° and a low water roll-off angle of around 3°. The prepared samples were characterized by powder X-ray diffraction（XRD）, X-ray photoelectron spectroscopy （XPS）, energy-dispersive X-ray spectroscopy（EDX）, transmission electron microscopy（TEM）, and scanning electron microscopy（SEM）. SEM images of the films show that the resulting surface exhibits flower-shaped micro- and nano-structure. The surfaces of the prepared films were composed of ZnO nanorods which were wurtzite structure. The special flower-like micro- and nano-structure along with the low surface energy leads to the surface superhydro- phobicity.

Chemical Analysis Method for Carbon Bearing Refractory Products——Determination of Magnesium Oxide Content by CyDTA Volumetric Method

This standard specifies the method summary, reagents, apparatus, sampling, procedure, test results calculation and permissible tolerance of the determination of magnesium oxide by CyDTA volumetric method.

A FACILE CHEMICAL SYNTHESIS of PENTADEOXYRIBONUCLEOTIDE d-TGGGT via PHOSPHOTRIESTER METHOD

In this paper,we report the chemical synthesis of oligonucleotide d-TGGGT using phosphotriester method.The protected pentamer d-MmtTGibGibGibT(=p-ClC6H_4-O(O)P)was deblocked by treatment with concentrated ammonium hydroxide and 80% acetic acid.The pure d-TGGGT obtained by chromatorgraphy on DEAE-Sephadex A-25 and Q-Sepharose FF could be hydrolyzed completely and confirmed by base ratio.

Different Methods of Analysis for the Identification of Materials Dated to Different Periods in Egypt

Different questions may be raised during the course of analysis concerning in particular the characterization of materials used, their preparation and application techniques. The different methods used to identify the materials of mud brick, limestone, plaster, mortar and pigments, collected from different sites and periods from Egypt, in order to identify and characterize the materials, their structure, composition and their mineralogical compounds were： （Op） optical microscopy, which was used to examine and to identify the materials structures. Methods used in initial examination were： （1） （MCA）： Micro-chemical analysis, to identify the nature of the materials and for water-soluble salts, to identify sulphates, chlorides, carbonates, nitrites and nitrates; （2） （SM）： Standard methods of wet chemical analysis were used to identify the quantitative and qualitative nature of the, mud building, mortars and their mixtures; （3） （SEM ＆ EDS）： Analytical scanning electron microscope with energy dispersive X-ray analysis system was used to examine the micro-morphology and determine the chemical composition of the different materials; （4） （XRD ＆ XRPD）： X-ray diffraction to identify the mineralogical compound of the plaster, limestone, mortars and pigments used. From all the results obtained, it was possible to establish the nature of the mortars and their binders as well as some other inclusion. In addition to the identification of the stratigraphy of the layers applied in some samples, the examination and analysis gave details of the materials and the approximate ratio of the amount of additives used. Furthermore, the mineralogical analysis provided information on the main mineralogical phases present in the materials analyzed from the different periods.

Binding Media： Methods of Identification： Part 1, Theoretical Work

The identification of binding media presents a major difficulty in the investigation of painting techniques. The materials used in ancient times as a media for the pigments were varied, such as glues, gums and egg white. These adhesives were mixed with the pigments to adhere to the surface or to prepare the ground. This medium serves to protect the pigments more or less perfectly, from chemical and mechanical injury. Binding media determines the technique of painting. Artists＇ techniques used through the centuries differ more in the binding media than in the pigments used. They are all organic substances containing the same common elements, and in the small samples which can be removed from paintings, occur only in micro quantities, moreover, binding media undergo considerable degradation over long periods of time. In the examination of works of art, only very small specimens can be taken and, the proportion of binding medium to pigment being small, sensitive methods of analysis have to be adopted in an attempt to detect and identify the medium that may have been used. On the other hand, the use of such methods possesses the disadvantage that impurities present in the painting materials may also be detected and may lead to erroneous conclusions. There is no general microanalysis technique existed in the identification of binding media, and the materials commonly used as media are highly complex compared with the simple inorganic compounds employed as pigments. However, several methods can be used in the identification of binding media such as micro-chemical, chemical and physical methods.