Data fusion of Fourier transform infrared spectra and powder X-ray diffraction patterns for pharmaceutical mixtures

2011 ◽  
Vol 56 (5) ◽  
pp. 944-949 ◽  
Author(s):  
Rahul V. Haware ◽  
Patrick R. Wright ◽  
Kenneth R. Morris ◽  
Mazen L. Hamad
Keyword(s):  
Fourier Transform ◽  
Data Fusion ◽  
Infrared Spectra ◽  
Fourier Transform Infrared ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fourier Transform Infrared Spectra ◽  
Diffraction Patterns

scholarly journals Regioselective Approach to Characterizing Increased Edge Availability in Layered Crystal Materials following Layer Expansion: Reaction of Kaolinite with Octadecyltrimethylammonium Salts

Materials ◽  
2022 ◽  
Vol 15 (2) ◽  
pp. 588
Author(s):  
Shingo Machida ◽  
Ken-ichi Katsumata ◽  
Atsuo Yasumori
Keyword(s):  
Fourier Transform ◽  
Mass Loss ◽  
Nitrogen Content ◽  
Infrared Spectra ◽  
Layered Crystal ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermogravimetric Curve ◽  
Diffraction Patterns ◽  
The Fourier Transform

In this paper, the regioselective reactions of kaolinite and methoxy-modified kaolinite (MeO-Kaol), methanol-expanded kaolinite, with octadecyltrimethylammonium salts are compared. This study mainly concerns the reactions of kaolinite or MeO-Kaol with octadecyltrimethylammonium chloride (C18TAC) in methanol and the subsequent exhaustive washing of the resultant products with ethanol. X-ray diffraction patterns of the products reveal no intercalation of C18TAC between pristine kaolinite layers. Additionally, intercalation and subsequent deintercalation of C18TAC proceed in the product using MeO-Kaol. In the Fourier-transform infrared spectra, the intensities of CH2 stretching bands of the product prepared using MeO-Kaol drastically increase compared to those using kaolinite. In addition, CH2 stretching bands of the product using kaolinite are hardly observed without enlarging the spectrum. The product using MeO-Kaol also displays mass loss in the range of 200–300 °C in the thermogravimetric curve and a nitrogen content with 0.15 mass% estimated using the CHN analysis. These results therefore demonstrate an increase in the available reactive edges in the layered crystal material following an expansion of the stacked layers.

Review of the application of ionic liquids as solvents for chitin

2012 ◽  
Vol 32 (2) ◽  
Author(s):  
Malgorzata M. Jaworska ◽  
Tomasz Kozlecki ◽  
Andrzej Gorak
Keyword(s):  
Fourier Transform ◽  
Ionic Liquids ◽  
Microwave Irradiation ◽  
Infrared Spectra ◽  
Elevated Temperatures ◽  
Great Promise ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Crystallinity ◽  
Diffraction Patterns

Abstract Chitin is one of the most abundant biopolymers, but due to its high crystallinity, it is completely insoluble in most organic and inorganic solvents. Chitin is soluble only in solvents that can destroy intersheet and intrasheet H-bonds, and many of these solvents are toxic, corrosive, nondegradable, or mutagenic. Because of these drawbacks, there is a search for more environmentally friendly solvents for chitin. It has been shown that ionic liquids (ILs) can dissolve chitin at elevated temperatures (80°–110°C) or with application of microwave irradiation. The highest solubility of chitin in an IL was about 20% (1-ethyl-3-methylimidazolium acetate), whereas chitin was shown to be insoluble in 1-allyl-3-methylimidazolium chloride and 1-butyl-3-methylimidazolium formate. Dissolved chitin can be regenerated by mixing with water or methanol, where the polymer precipitates from the solution. X-ray diffraction patterns of native polymer and precipitates have been compared and only small changes in crystallinity have been observed. In addition, Fourier transform infrared spectra remained similar for both forms of chitin, native and regenerated. Presented data hold great promise for the improvement of the chemistry of chitin and open new routes for chemical and enzymatic modifications of this polymer.

scholarly journals Chromium (III) Oxide Nanostructures Synthesized from Vernonia Amygdalina Leaves Extract

2020 ◽  
Vol 10 (1) ◽  
pp. 1856-1861
Keyword(s):  
Fourier Transform ◽  
Average Crystallite Size ◽  
Fourier Transform Infrared ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Vernonia Amygdalina ◽  
Sem Images ◽  
X Ray ◽  
Chloride Hexahydrate ◽  
Diffraction Patterns

This contribution reports first time synthesis of Cr2O3 nanostructures from chromium (III) chloride hexahydrate precursor using Vernonia amygdalina leaves extract as a reducing and stabilizing agent. Powder X-ray diffraction, Fourier-transform infrared spectroscopy, and scanning electron microscopy techniques were used to study the structural and morphological properties of the as-synthesized Cr2O3 nanostructures. Powder X-ray diffraction patterns spectral analysis showed that hexagonal Cr2O3 nanostructures with an average crystallite size of 23.4 nm were synthesized with the minor appearance of CrO2. SEM images showed that the synthesized nanomaterials are granules. Fourier-transform infrared spectra represent a sharp absorption band at 552 cm-1, which indicates Cr-O-Cr vibrational and stretching modes.

PENINGKATAN LAJU DISOLUSI ACYCLOVIR DENGAN METODE SISTEM DISPERSI PADAT MENGGUNAKAN POLOXAMER 188

2016 ◽  
Vol 5 (1) ◽  
pp. 6
Author(s):  
Budi Setiawan ◽  
Erizal Zaini ◽  
Salman Umar
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Differential Thermal Analysis ◽  
Fourier Transform Infrared ◽  
X Ray Diffraction ◽  
Poloxamer 188 ◽  
X Ray ◽  
Scanning Electron

Sebuah penelitian tentang sistem dispersi padat dari asiklovir dengan poloxamer 188 telah dilakukan formulasi dengan pencampuran secara fisika dengan rasio 1 : 1, 1 : 3, 1 : 5 dan dispersi padat 1 : 1, 1 : 3, 1 : 5 dan penggilingan 1:1 sebagai pembanding. Dispersi padat dibuat menggunakan metode pencairan (fusi), yang digabung dengan poloxamer 188 pada hotplate kemudian asiklovir dimasukkan ke dalam hasil poloxamer 188 lalu di kocok hingga membentuk masa homogen. Semua formula yang terbentuk termasuk asiklovir poloxamer 188 murni dianalisis karakterisasinya dengan Differential Thermal Analysis (DTA), X-ray Diffraction, Scanning Electron Microscopy (SEM), dan Fourier Transform Infrared (FTIR), kemudian pengambilan dilakukan  (penentuan kadar) mengunakan spektrofotometer UV pada panjang gelombang 257,08 nm dan uji laju disolusi dengan aquadest bebas CO2 menggunakan metode dayung. Hasil pengambilan  (penentuan kadar) menunjukkan bahwa semua formula memenuhi persyaratan farmakope Amerika edisi 30 dan farmakope Indonesia edisi 4 yaitu 95-110%. Sedangkan hasil uji laju disolusi untuk campuran fisik 1: 1, dan dispersi padat 1: 1, dan penggilingan 1: 1 menunjukkan peningkatan yang nyata dibandingkan asiklovir murni. Hal ini juga dapat dilihat dari hasil perhitungan statistik  menggunakan analisis varian satu arah  SPSS 17.

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