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Preparation of Activated Carbon from Sugarcane Bagasse Waste for the Adsorption Equilibrium and Kinetics of Basic Dye Tawan Chaiwona, Panatda Jannoeyb, Duangdao Channeic* aDepartment of Chemistry and General Science, Faculty of Education, Valaya Alongkorn Rajabhat University under the Royal Patronage, Pathum Thani 13180, Thailand bDepartment of Biochemistry, Faculty of Medical Science, Naresuan University, Phitsanulok, 65000, Thailand *cDepartment of Chemistry, Faculty of Science, Naresuan University, Phitsanulok 65000, Thailand *E-mail: duangdaoc@nu.ac.th (Corresponding author: Duangdao Channei) Keywords: Activated carbon, Sugarcane Bagasse, Adsorption Isotherm, Adsorption kinetics Abstract.
Activated carbons prepared through chemical activation using acid and/or basic activating agents has been reported as more advantages over physical activation due to its larger specific surface area, higher yields, simpler production process and highly developed porous structure [8].
Ismadji, Activated carbon from jackfruit peel waste by H3PO4 chemical activation: Pore structure and surface chemistry characterization, Chem.

Water-soluble phosphates and fluorides contribute to the formation of the structure of gypsum products with increased strength and water resistance [2,3].
Physical and mechanical tests carried out within the time specified by the standard do not provide information on the properties of the binder, since the process of structure formation has not ended.
M .: Chemistry, 1990. 224 p
University "KhPI": Sat scientific tr Theme. issue: Chemistry, chemical technology and ecology. - Kharkov: NTU "KhPI", 2008. - No. 33. - P. 159-162
Kinetic-mathematical model of hydration of lime-silica binder, wich activated together with a fine-grained filler // Proceeding of 13th International Congress on the Chemistry of Cement. – Madrid, Spain 2-8 July 2011.

In this study, activated by epoxy chloropropane, the magnetite core/functional organic shell structured particles are characterized in terms of chemical composition, particle size and electrophoretic mobility and act as the immobilized PGA carriers.
Firstly, the PAA, as the competitive inhibitor of PGA, could keep the structure of active center of PGA and decrease the loss of PGA activity in the reaction system.
Vogel: Analytical Chemistry.
Fernandez-Lafuente and Mateo C: Bioorganic and Medicinal Chemistry Letters.
Danov and N.D.Denkov: Handbook of Surface and Colloid Chemistry (CRC Press, USA 1997)

Conclusions DSC can not provide any direct information about the chemical composition and structure of natural resins and waxes.
These thermodynamic properties are sensitive to the chemical composition and structure of the resins and waxes, and thus can be used in the identification of natural resins and waxes.
The chemistry of neolithic beeswax.
The organic chemistry of museum objects of butterworths, London
Journal of Polymer Science Part A: Polymer Chemistry, 1998, 35(13):2063-2071 [15] D.

Scheme 1 Structures of synthesized DOPO-based phosphonamidates.
The peak at 1290 cm-1 is attributed to the P=O stretching vibration of the O=P-O-Φ structure, where Φ represents a polynuclear aromatic structure.
The bands at 1080 and 750 cm-1 is assigned to the stretching vibrations of P-O-P structure and out-of-plane bending vibrations of aromatic C-H for P-O-Φ complex structure [22].
Hamerton, Recent developments in the chemistry of halogen-free flame retardant polymers, Prog.
Gaan, An overview of some recent advances in DOPO-derivatives: Chemistry and flame retardant applications, Polym.

The Ba6-3xR8+2xTi18O54 solid solutions have an orthorhombic tungstenbronze type-like structure with lattice parameter a≈1.22 nm, b≈2.23 nm, c≈0.77 nm.
Materials with large anisotropy in the crystal structure can be applied the texture engineering to obtain the single crystal-like properties [4, 5].
To clearly understand the correlation between the crystal structure and dielectric properties, evaluation of highly grain-oriented Ba6-3xR8+2xTi18O54 is a important subject of research.
Fig. 1 Crystal structure of BSmT; (a) ab-plane (b) ac-plane.
Davies, "Influence of Chemistry and Processing on the Electrical Properties of Ba6-3xLn8+2xTi18O54 Solid Solutions," Ceramic Transactions, Vol. 53, Materials and Process for Wireless Communications, Edited by T.

TiO2: from nanotubes to nanopores by changing the anodizing voltage in floride-glycerol electrolyte Claudiu Constantin Manole1, a , Cristian Pirvu1,b, and Ioana Demetrescu1,c 1 Faculty of Applied Chemistry and Materials Science, University Politehnica Bucharest Str.
For the nanostructures growth at 80V the wider distribution of the structures generates a bigger amount of irregularities.
With the increase in voltage, the ordered structures shift from nanotubular aspect towards a porous distribution on the surface.
At 40V applied voltage, the nanotubes are incorporated by porous structures of the same diameter.
With the increase in voltage, the ordered structures shift from nanotubular aspect towards a porous distribution over the surface.

Journal of Physical Chemistry, 2002, 64(1): 95-98
Journal of Molecular Structure, 2016, 1117: 105-112
Journal of Fluorine Chemistry, 2016, 185: 42-47
Local structure of liquid CaAl 2O 4 from ab initio molecular dynamics simulations[J].
Journal of Physical Chemistry B Condensed Matter Materials Surfaces Interfaces & Biophysical, 2014

The results of EDX analyzes of the best hNF-PON1 structure showed that these structures had higher percentage O (30.2%), P (23.6%), and Ca (23.4%) elements compared hNF-PON1 structures obtained in other pHs.
XRD Patterns of Hybrid Nanoparticles PON1 Structures The FT-IR spectra of the hybrid NF PON1 enzyme structure was presented in Figure 9.
Journal of Material Chemistry 15, 3745–3760. doi: 10.1039/b505099e [3] Du, J., O’Reilly, R.K. (2011) Anisotropic particles with patchy, multicompartment and Janus architectures: Preparation and application.
Jornal of Biological Chemistry 164, 271–289
Clinical Chemistry 52:453–457. doi: 10.1373/clinchem.2005.063412 [34] Kharisov, B. (2008) A Review for Synthesis of Nanoflowers.

Wurst3 1 Institute of Mineralogy & Petrography, University of Innsbruck, Austria 2 Institute of Pharmacy, University of Innsbruck, Austria 3Institute of General, Inorganic and Theoretical Chemistry, University of Innsbruck, Austria Keywords: indinavir, indinavir sulphate, crystal properties, crystal structure, urinary stones Introduction The treatment of the human immunodeficiency virus (HIV) infection has been extremely improved by the introduction of a new class of anti-HIV-drugs, the protease inhibitors [1].
The structure was solved with direct methods and refined against F2 using the SHELX program suite.
Fig. 3: Thermal ellipsoid plot of the molecular structure of indinavir monohydrate.
Crystal structure of indinavir base and calculated powder pattern Fig. 3 shows the molecular structure of indinavir with the hydrogen bond between the water molecule and the pyridine moiety, N(4)…HO(5).
The crystal structure of the monohydrate was determined and based on the reflections of the calculated powder pattern it is now possible to clearly identify indinavir monohydrate as a potential component in urinary stones from HIV-patients with X-ray powder diffractometry.