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Chromatographic, Spectroscopic, and Thermal Characterization of Biofield Energy Treated N,N-Dimethylformamide

机译:生物场能量处理过的N,N-二甲基甲酰胺的色谱,光谱和热表征

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N,N-Dimethylformamide (DMF) is a ‘universal’ solvent and has wide variety of applications in organic synthesis, purification, crystallization, and as cross-linking agent. The aim of this study was to evaluate the physicochemical and spectroscopic properties of DMF after the biofield energy treatment using various analytical techniques. DMF sample was divided into two parts, one part (control) remained as untreated, while the other (treated) part was treated with Mr. Trivedi’s biofield energy treatment. The treated sample was subdivided into three parts named as T1, T2, and T3 for gas chromatography-mass spectrometry (GC-MS) analysis. Five relatively intense peaks were observed in the mass spectrum of both control and treated samples of DMF. The GC-MS data revealed that the isotopic abundance ratio of (PM+1)/PM in DMF was slightly decreased by 5.76% in T1, and increased by 48.73%, and 30.17% in T2, and T3 samples, respectively as compared to the control [where, PM- primary molecule, (PM+1)- isotopic molecule either for sup13/supC or sup2/supH or sup15/supN]. Similarly, the isotopic abundance ratio of (PM+2)/PM was decreased by 10.34% in T1 and then increased upto 43.67% (T2) as compared to the control [where, (PM+2)- isotopic molecule for sup18/supO]. In high performance liquid chromatography (HPLC), the treated DMF showed similar retention time (TsubR/sub) as compared to the control with an additional small peak at 2.26 min appeared in the treated sample. In DSC thermogram the heat change in a sharp endothermic transition at around 61°C of treated DMF was increased by 152.56% as compared to the control. Further, C=O and C-N stretching frequencies of treated sample were shifted by 7 cmsup-1/sup and 3 cmsup-1/sup, respectively towards low energy region in Fourier transform infrared (FT-IR) spectroscopy. These results suggested that biofield energy treatment has significantly altered the physical and spectroscopic properties of DMF, which could make them more stable solvent in organic synthesis and as a suitable formulation agent in polymer/paint industry.
机译:N,N-二甲基甲酰胺(DMF)是一种“通用”溶剂,在有机合成,纯化,结晶以及用作交联剂方面具有广泛的应用。这项研究的目的是使用各种分析技术评估生物场能量处理后DMF的物理化学和光谱性质。 DMF样品分为两部分,一部分(对照)保持未经处理,而另一部分(处理)则用Trivedi先生的生物场能量处理剂处理。将处理后的样品分为三部分,分别称为T1,T2和T3,用于气相色谱-质谱(GC-MS)分析。在对照和处理过的DMF样品的质谱图中观察到五个相对强烈的峰。 GC-MS数据显示,与之相比,DM1中(PM + 1)/ PM的同位素丰度比在T1中略微降低了5.76%,在T2和T3中分别增加了48.73%和30.17%。对照[其中, 13 C或 2 H或 15 N的PM-初级分子,(PM + 1)-同位素分子” 。同样,与对照组相比,T1中(PM + 2)/ PM的同位素丰度比降低了10.34%,然后增加至43.67%(T2)[其中,的(PM + 2)-同位素分子18 O]。在高效液相色谱(HPLC)中,与对照相比,处理后的DMF表现出相似的保留时间(T R ),并且在处理后的样品中出现了一个在2.26分钟处的附加小峰。在DSC热分析图中,与对照相比,在约61℃下,经处理的DMF在急剧的吸热转变中的热变化增加了152.56%。此外,在傅立叶变换红外(FT)中,处理样品的C = O和CN拉伸频率分别向低能区偏移7 cm -1 和3 cm -1 -IR)光谱。这些结果表明,生物场能量处理已大大改变了DMF的物理和光谱性质,从而使其在有机合成中更稳定地成为溶剂,并在聚合物/涂料工业中用作合适的配制剂。

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