Gunin Saikia

Physical and Structural Characterization of Biofield Treated Imidazole Derivatives

Imidazole derivatives have attracted significant interests in recent time for their usefulness in synthetic heterocyclic chemistry, analytical chemistry and pharmacology. Aim of present study was to evaluate the impact of biofield treatment on two imidazole derivatives (i.e., imidazole and 2-methylimidazole) by various analytical methods. The biofield treatment was done by Mr. Trivedi on both the compounds and both control and treated samples of imidazole and 2-methylimidazole were characterized with respect to physical, and structural properties using X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR), ultraviolet-visible (UV-Vis) spectroscopy, and Gas chromatography-Mass spectrometry (GC-MS). X-ray diffraction study revealed that crystallite size varied in a different way for imidazole and 2-methylimidazole due to the presence of methyl group in 2-c position although their core was same. Treated sample of imidazole showed a slight increase in crystallite size (6.5%); however, treated 2-methylimidazole showed a significant increase (166.68%) in crystallite size along with decrease in peak intensity as compared to control. The latent heat of fusion (ΔH) of imidazole was increased up to 0.62% in treated sample as compared to control; whereas in treated 2-methylimidazole, the ΔH was decreased by 22% as compared to control. Maximum degradation temperature (Tmax) from TGA of imidazole was remained same but 2-methylimidazole was increased by 1.5% as compared to control. FT-IR spectra showed slight change in stretching frequencies of treated imidazole and 2-methylimidazole as compared to control. Both the imidazole and 2-methylimidazole showed similar UV absorbance maxima as compared to respective control sample. GC-MS data revealed that isotopic abundance ratio of either 13C/12C or 15N/14N or 2 H/1 H (PM+1/PM) of treated imidazole was significantly increased up to 232.51% as compared to control, however, isotopic abundance ratio of 13C/12C or 15N/14N or 2 H/1 H (PM+1/PM) of treated 2-methylimidazole showed a minor change from -1.68 upto 1.68% as compared to control. Overall, the experimental results suggest that biofield treatment has significant effect on structural and thermal properties of imidazole and 2-methylimidazole.

Influence of Biofield Energy Treatment on Isotopic Abundance Ratio in Aniline Derivatives

The aim of this study was to evaluate the impact of biofield energy treatment on the isotopic abundance of 13C/12C or 2H/1H or 15N/14N ≡ (PM+1)/PM in aniline; and (PM+1)/PM and 81Br/79Br ≡ (PM+2)/PM in 4-bromoaniline using Gas Chromatography-Mass Spectrometry (GC-MS). Aniline and 4-bromoaniline samples were divided into two parts: control and treated. The control part remained as untreated, while the treated part was subjected to Mr. Trivedi’s biofield energy treatment. The treated samples were subdivided in three parts named as T1, T2, and T3 for aniline and four parts named as T1, T2, T3, and T4 for 4-bromoaniline. The GC-MS data revealed that the isotopic abundance ratio of (PM+1)/PM in aniline was increased from -40.82%, 30.17% and 73.12% in T1, T2 and T3 samples respectively. However in treated samples of 4-bromoaniline the isotopic abundance ratio of PM+1/PM was increased exponentially from -4.36 % (T1) to 368.3% (T4) as compared to the control. A slight decreasing trend of the isotopic ratio of (PM+2)/ PM in 4-bromoaniline was observed after biofield energy treatment. The GC-MS data suggests that the biofield energy treatment has significantly increased the isotopic abundance of 2H, 13C and 15N in the treated aniline and 4-bromoaniline, while slight decreased the isotopic abundance of 81Br in treated 4-bromoaniline as compared to their respective control.

Isotopic Abundance Analysis of Biofield Treated Benzene, Toluene and p -Xylene Using Gas Chromatography-Mass Spectrometry (GC-MS)

Benzene, toluene and p-xylene are derivatives of benzene, generally produced from crude petroleum and have numerous applications in industry. The aim of the present study was to evaluate the impact of biofield treatment on isotopic abundance of these benzene derivatives by gas chromatography-mass spectrometry (GC-MS). Benzene, toluene and p-xylene samples were divided into two parts: control and treatment. Control part was remained as untreated and treatment part was subjected to Mr. Trivedi’s biofield treatment. Control and treated samples were characterized using GC-MS. GC-MS data revealed that isotopic abundance ratio of 13C/12C or 2H/1H (PM+1/PM) of treated samples were significantly increased from un-substituted to substituted benzene rings (where, PM- primary molecule, PM+1- isotopic molecule either for 13C/12C and/or 2H/1H). The isotopic abundance ratio of 13C/12C or 2H/1H (PM+1/PM) in benzene was decreased significantly by 42.14% as compared to control. However, the isotopic abundance ratio of (PM+1/PM) in treated toluene and p-xylene was significantly increased up to 531.61% and 134.34% respectively as compared to their respective control. Thus, overall data suggest that biofield treatment has significantly altered the isotopic abundance ratio of (PM+1/PM) in a different way for un-substituted and substituted benzenes.

Thermal, Spectroscopic and Chemical Characterization of Biofield Energy Treated Anisole

The objective of the present study was to evaluate the impact of biofield energy treatment on the thermal, spectroscopic, and chemical properties of anisole by various analytical methods such as gas chromatography-mass spectrometry (GC-MS), high performance liquid chromatography (HPLC), differential scanning calorimetry (DSC), Fourier transform infrared (FT-IR) spectroscopy, and ultraviolet-visible (UV-Vis) spectroscopy. The anisole sample was divided into two parts, control and treated. The control part was remained same while the other part was treated with Mr. Trivedi’s unique biofield energy treatment. Mass spectra showed the molecular ion peak with five fragmented peaks in control and all treated samples. The isotopic abundance ratio of 2H/1H, and 13C/12C [(PM+1)/PM] in treated sample was increased by 154.47% (T1) as compared to the control [where, PM- primary molecule, (PM+1)-isotopic molecule either for 13C or 2H]. The HPLC chromatogram showed retention time of treated anisole was slightly decreased as compared to the control. Moreover, the heat change in the sharp endothermic transition of treated anisole was increased by 389.07% in DSC thermogram as compared to the control. Further, C-C aromatic stretching frequency of treated sample was shifted by 2 cm-1 to low energy region in FT-IR spectroscopy. The UV-Vis spectra of control sample showed characteristic absorption peaks at 325 nm, which was red shifted and appeared as shoulder in the treated sample. These results suggested that biofield treatment has significantly altered the physical and spectroscopic properties of anisole, which could make them stable solvent for organic synthesis and as a suitable reaction intermediate in industrial applications.