Bio-Based Graphene Sheet/Copolymer Composite as Supporting Material for Nanocatalysts towards Electrochemical Studies and Direct Alkaline Alcohol Fuel Cells

In this work, graphene carbon sheets (BGS) were prepared from writing paper and lemon peel, and its polymer composite has a higher surface area compared with the existing Vulcan carbon. Further, the use of lead as a promoter for the oxidation of alcohol and CO on platinum-supported poly(amine-terminated cyclophosphazene-co-cyclophosphazene)-biobased graphene sheet (Poly(AFCP-co-CP)-BGS) composite was demonstrated. The size, phase morphology, and distribution of metal nanoparticles on Poly(AFCP-co-CP)-BGS composite as well as the formation of composite based catalysts were confirmed from TEM, XRD, and FTIR studies. The catalytic activity and stability of the prepared catalysts were tested and compared to methanol, ethylene glycol, glycerol, and CO in 0.5 M KOH solution. The results conclude that the lead-doped Pt/Poly(AFCP-co-CP)-BGS catalyst shows higher oxidation current with respect to onset potential and lower I f / I r ratio for alcohol as well as CO oxidation. In addition, Pt-Pb/Poly(AFCP-co-CP)-BGS catalyst was checked for direct alkaline fuel cells and proved as a potent anode catalyst in alkaline medium for real-time fuel battery applications. In addition, Poly(AFCP-co-CP)-BGS composite also promotes the catalytic reaction compared to Poly(AFCP-co-CP) and BGS supports as noticed from methanol oxidation in alkaline medium. The surface area of the prepared supporting material is 750.72 m2g-1, which is higher than the activated carbon (250.12m2g-1). So, the prepared Poly(AFCP-co-CP)-BGS composite is a potent support for metal deposition, electrooxidation, and single stack fuel cell constructions.

Formulation and Evaluation of Fast Dissolving Tablet of Ondansetron by Utilizing Liquisolid Compact Technique

Ondansetron is an anti-emetic drug which is insoluble in water. The present study was aimed to formulate and evaluate oral fast dissolving tablet of Ondansetron by Utilizing Liquisolid Compact Technique. The tablets were prepared by direct compression method and characterized by UV, FTIR studies. Six formulations (F1-F6) of ondansetron were prepared and tablets were evaluated for weight variations, hardness, thickness, friability, disintegration time, drug content and In-vitro dissolution studies gave satisfactory result. TF6 was found to be the best and acceptable formulation whose drug content was about 99.17±0.05 and percentage (%) drug release 97.49±2.03 in 10 min, high as compare to other formulation and has low disintegration time 17±0.01 as compare to other formulation which indicates that drug is rapidly dissolved and available at the site of action.

Formulation and evaluation of oral disintegrating tablets of furosemide

Orally disintegrating tablets of Furosemide were prepared, evaluated and the comparison of the action of different concentrations of disintegrants on disintegration and dissolution of the tablets were studied. Direct compression method was used to prepare the orally disintegrating tablets containing 20 mg of Furosemide. The formulation was conducted using different concentrations of crospovidone, croscarmellose and sodium starch glycolate as superdisintegrants and their interactions with Furosemide were also evaluated using FTIR. FTIR studies using the drug and its mixtures with the excipients showed that the peaks correlate with one another which signify that there is no interaction between the drug molecule and the excipients used. The obtained results revealed that the disintegration time of ODTs were between 9 to 59 seconds. The percentage drug content of tablets in all the formulations was found between 91.51% to 106.69%, which complies with the limits established in pharmacopoeia. The in-vitro dissolution studies show maximum release of 89.47% in formulation F3 and minimum of 77.64% in formulation F12. Higher concentration of crospovidone and croscarmellose in formulations F3 and F6 showed better dissolution properties than SSG. So by varying the concentrations of superdisintegrants, oral disintegrating tablets can be formulated.

Structural and Infrared Spectroscopy of Polyvinylpyrrolidone/Multi-walled Carbon Nanotubes Nanocomposite

In this work, polyvinylpyrrolidone (PVP)/ Multi-walled carbon nanotubes (MWCNTs) nanocomposites were prepared with two concentrations of MWCNTs by casting method. Morphological, structural characteristics and electrical properties were investigated. The state of MWCNTs dispersion in a PVP matrix was indicated by Field Effect-Scanning Electron Microscopy (FESEM) which showed a uniform dispersion of MWCNTs within the PVP matrix. X-ray Diffraction (XRD) indicate strong bonding of carbonyl groups of PVP composite chains with MWCNTs. Fourier transfer infrared (FTIR) studies shows characteristics of various stretching and bending vibration bands, as well as shifts in some band locations and intensity changes in others. Hall effect was studied to test the type of charge carriers which was shown to be P-type. The electrical conductivity was shown increased for the pure PVP and pure MWCNT from (2.047×10-5) (Ω.cm)-1 and (3.683×101) (Ω.cm)-1 to (2.51×102 and 2.36×102) (Ω.cm)-1for both concentrations of nanocomposites, which indicate the conductivity was enhancement by using the carbon nanotubes.

The Nature of Zeolite Catalytic Sites

<p>The nature of zeolite catalytic sites was studied by observing their interactions with sorbants. In situ FTIR studies of a range of sorbants on H+ZSM-5, H+mordenite and H+Y showed that the zeolite Bronsted proton was transferred towards the sorbant. Sorbants could be placed in three classes depending on the type of hydrogen bond formed. "Class A" sorbants were alcohols, alkanes, ammonia, amines and carboxylic acids and showed a single v0-H band shifted from the vO-H of the zeolite. The shift in vO-H increased with increasing proton affinity of the sorbant. "Class B" sorbants were alkenes and aromatics and showed a resultant broad, flat vO-H due to bonding through the t electrons of the double bond or aromatic ring. "Class C" sorbants included water, ethers, ketenes, aldehydes, nitriles and carboxylic acids (also Class A). They showed extremely broad hydroxyl bands from -3700 to -1200 cm-1 with several maxima. Bonding was through oxygen or nitrogen lone electron pairs. A novel, low temperature (-400 [degrees] C), reaction of acetic acid to ketene was observed over alkali-exchanged zeolites. Thermal desorption/mass spectrometry, mini-reactor mass spectrometry and in situ FTIR techniques were used to investigate the products obtained by varying the carboxylic acid and the catalyst, and the reaction mechanism.</p>

The Nature of Zeolite Catalytic Sites

<p>The nature of zeolite catalytic sites was studied by observing their interactions with sorbants. In situ FTIR studies of a range of sorbants on H+ZSM-5, H+mordenite and H+Y showed that the zeolite Bronsted proton was transferred towards the sorbant. Sorbants could be placed in three classes depending on the type of hydrogen bond formed. "Class A" sorbants were alcohols, alkanes, ammonia, amines and carboxylic acids and showed a single v0-H band shifted from the vO-H of the zeolite. The shift in vO-H increased with increasing proton affinity of the sorbant. "Class B" sorbants were alkenes and aromatics and showed a resultant broad, flat vO-H due to bonding through the t electrons of the double bond or aromatic ring. "Class C" sorbants included water, ethers, ketenes, aldehydes, nitriles and carboxylic acids (also Class A). They showed extremely broad hydroxyl bands from -3700 to -1200 cm-1 with several maxima. Bonding was through oxygen or nitrogen lone electron pairs. A novel, low temperature (-400 [degrees] C), reaction of acetic acid to ketene was observed over alkali-exchanged zeolites. Thermal desorption/mass spectrometry, mini-reactor mass spectrometry and in situ FTIR techniques were used to investigate the products obtained by varying the carboxylic acid and the catalyst, and the reaction mechanism.</p>

A Process of Electrohomeopathic remedy “SLASS” Preparation, Compared with Krauss Method By phytochemical Analysis, TLC and FTIR Studies

Electrohomeopathy medicines have been practicing since the 1850s in European countries and from the 1870s in India. There are various methods of preparation of Electrohomeopathic medicines that have been developed and practice by the different manufacturers. For the safety, efficacy, and stability of the medicines, there is a need for scientific research to standardize the procedure of medical preparations. SLASS is one of the commonly using remedy by the electro homeopathy practitioners for various disorders concern to the digestive system, excretory system and nervous system etc... In the present studies we attempted a comparative study of a Process of Electrohomeopathic remedy “SLASS” Preparation, Compared with the Krauss method by phytochemical analysis, TLC, and FTIR Studies. Our process and Krauss method showed significant differences in phytochemical profile TLC and FTIR spectral peaks. The yield of the extracts of Aloe capensis and Gentiana lutea are more in our method compared to Krauss method. Glycoside is present in Krauss method. These research outcomes with reproducibility will become standard markers or signatures to assess the quality, safety, and efficacy of the electro homeopathy medicine as well as reduce the risk of adulterations helps to develop specifications of the Electrohomeopathy remedies. Future work is essential to explore its therapeutic applications

Effect of ultrahigh diluted homeopathic medicines on the electrical properties of PVDF-HFP

In an effort to improve the electrical properties of the electroactive Poly(vinylidene fluoride-hexafluoropropylene) (PVdF-HFP), we introduced a novel and simple approach to synthesize PVDF-HFP composite films by incorporating ultrahigh dilutions of two homeopathic medicines Ferrum metallicum (FM) and Zincum oxidatum (ZO) in different potencies. The homeo-PVDF-composite films (HPCF) were synthesized by simple solution casting technique. XRD, FESEM, FTIR studies were performed to check the presence of nanoparticles in the film. The electrical properties of the HPCF samples get enhanced significantly due to the incorporation of the medicines and the effect increases with the increase in potency of the medicines.