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https://d1y502jg6fpugt.cloudfront.net/25425/archive/files/5a2d56776b577154d9d295e72e96ec93.pdf?Expires=1712793600&Signature=YRxn1LLnEEL9379fVf8cIELvPhRhP%7EWJJp5647tF-36oB20ETvDBtxxjSBeTFsLdEgU3zY6syCSVh3TSS0wwUPmPKNTpF8sZJpbPVeXGQOiEWbhXLTgJ9A9aNXtWEmJJtt4m%7ElV1Z5cIzvE9fA4fSSLRmPdpOldUkcMkUiAJt8KrdUMrBQW6h95%7Ea8uJaILHgGVSdeTqvUpADT1lYlFoam3gZzv6JOEDoAB%7EXHVcDtcXL1owSLo5CzbpZ943NLX8n-zqOYwE60LsuTgzv7hXrtuCtSFe9MNItF-IGGjdg7AtnJEn83qTnf-ECuy85PX%7EMEdrrXFvLLu6WGFVV47ftw__&Key-Pair-Id=K6UGZS9ZTDSZM
1d6b6c3c9be7ca979775eac71a031c15
Website
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<a href="https://www.trivedieffect.com/science/mass-spectrometry-analysis-of-isotopic-abundance-of-13c-2h-or-15n-in-biofield-energy-treated-aminopyridine-derivatives">https://www.trivedieffect.com/science/mass-spectrometry-analysis-of-isotopic-abundance-of-13c-2h-or-15n-in-biofield-energy-treated-aminopyridine-derivatives</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Mass Spectrometry Analysis of Isotopic Abundance of 13C, 2H, or 15N in Biofield Energy Treated Aminopyridine Derivatives
Subject
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Organic Compounds
Description
An account of the resource
<p style="text-align:justify;">2-Aminopyridine (2-AP) and 2,6-diaminopyridine (2,6-DAP) are two derivatives of aminopyridines that act as an important organic intermediates, mostly used in medicines, dyes and organic sensors. The aim of the study was to evaluate the impact of biofield energy treatment on isotopic abundance ratios of 2H/1H, 13C/12C, or 15N/14N, in aminopyridine derivatives using gas chromatography-mass spectrometry (GC-MS). The 2-AP and 2,6-DAP samples were divided into two parts: control and treated. The control sample remained as untreated, while the treated sample was further divided into four groups as T1, T2, T3, and T4. The treated group was subjected to Mr. Trivedi’s biofield energy treatment. The GC-MS spectra of 2-AP and 2,6-DAP showed five and six m/z peaks respectively due to the molecular ion peak and fragmented peaks of aminopyridine derivatives. The isotopic abundance ratio of 2H/1H, 13C/12C, or 15N/14N were calculated for both the derivatives and significant alteration was found in the treated samples as compared to the respective control. The isotopic abundance ratio of 2H/1H, 13C/12C, or 15N/14N in treated samples of 2-AP was decreased by 55.83% in T1 and significantly increased by 202.26% in T4. However, in case of 2,6-DAP, the isotopic abundance ratio of 2H/1H, 13C/12C, and 15N/14N, in the treated sample showed a significant increase (up to 370.54% in T3) with respect to the control. GC-MS data suggested that the biofield energy treatment on aminopyridine derivatives had significantly altered the isotopic abundance of 2H, 13C, or 15N in the treated 2-AP and 2,6-DAP as compared to the control.</p>
Creator
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Mahendra Kumar Trivedi, Alice Branton, Dahryn Trivedi, Gopal Nayak, Gunin Saikia, Snehasis Jana
Source
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<a href="http://www.sciencepublishinggroup.com/journal/paperinfo?journalid=128&doi=10.11648/j.ajpc.20150406.14" target="_blank" rel="noreferrer noopener">http://www.sciencepublishinggroup.com/journal/paperinfo?journalid=128&doi=10.11648/j.ajpc.20150406.14</a>
Publisher
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Science Publishing Group
Date
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December 22, 2015
Language
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English
Type
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Journal Article
Identifier
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10.11648/j.ajpc.20150406.14
2
2-Aminopyridine
6-Diaminopyridine
Biofield Energy Treatment
Gas Chromatography-Mass Spectrometry
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https://d1y502jg6fpugt.cloudfront.net/25425/archive/files/630dfdc55786dfd371a4553378b5fe5a.pdf?Expires=1712793600&Signature=I4pHlBwFGwULzw8ZhgPY3FVF7qiiE-0ZFMiV613QzPe0B6PNteUHzJBli%7EhDylXLp4Za7IQ58pfXE4K%7EhjMjp-uA8dQ-LgchLWCKozh6MXcM-q%7Eoz0ho4Nl1YKI%7EqvS3vSrHhtnk1WiGGteZDQjZQitBwMMyLDyGYswYbHqkY16rfkY9%7E3F-glhOOgswbKCc7S%7EjrujWMCiE10YgiHlNUtt3m15phG8du%7EN5BfcBGcxBhfhfa3wQhh-3Erw%7Eor422wyyuqaQSwMosRu1CMhzJz1JGkfjMA1yN5l-nCxARYoHSli1WeXkoS87K8CM2sfNlJ52l%7E19SigjoMOqHeDqxw__&Key-Pair-Id=K6UGZS9ZTDSZM
201ced11f8cb328a4da4445bd28f5c29
Website
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<a href="https://www.trivedieffect.com/science/characterization-of-physical-thermal-and-spectral-properties-of-biofield-treated-2-aminopyridine">https://www.trivedieffect.com/science/characterization-of-physical-thermal-and-spectral-properties-of-biofield-treated-2-aminopyridine</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Characterization of Physical, Thermal and Spectral Properties of Biofield Treated 2-Aminopyridine
Subject
The topic of the resource
Organic Compounds
Description
An account of the resource
<p style="text-align:justify;">2-Aminopyridine is an important compound, which is used as intermediate for the synthesis of pharmaceutical compounds. The present work was aimed to assess the effect of Mr. Trivedi’s biofield energy treatment on the physical, thermal and spectral characteristics of 2-AP. The work was accomplished by dividing the sample in two parts i.e. one part was remained untreated, and another part had received biofield energy treatment. Subsequently, the samples were analyzed using various characterization techniques such as X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, ultra violet-visible spectroscopy, and Fourier transform infrared spectroscopy. The XRD analysis revealed a decrease in crystallite size of the treated sample (91.80 nm) as compared to the control sample (97.99 nm). Additionally, the result showed an increase in Bragg’s angle (2θ) of the treated sample as compared to the control. The DSC and Differential thermal analysis analysis showed an increase in melting temperature of the treated 2-AP with respect to the control. Moreover, the latent heat of fusion of the treated sample was increased by 3.08%. The TGA analysis showed an increase in onset of thermal degradation (Tonset), and maximum thermal decomposition temperature (Tmax) of the treated 2-AP as compared to the control sample. Additionally, the treated sample showed a reduction in weight loss as compared with the control indicating higher thermal stability of the sample. UV-visible analysis showed no changes in the absorption peak of the treated sample as compared to the control. The FT-IR spectroscopic results showed downward shifting of C-H stretching vibration 2991→2955 cm-1 in treated sample with respect to the control.</p>
Creator
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Mahendra Kumar Trivedi, Alice Branton, Dahryn Trivedi, Gopal Nayak, Rakesh Kumar Mishra, Snehasis Jana
Source
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<a href="http://www.sciencepublishinggroup.com/journal/paperinfo?journalid=223&doi=10.11648/j.sjac.20150306.18" target="_blank" rel="noreferrer noopener">http://www.sciencepublishinggroup.com/journal/paperinfo?journalid=223&doi=10.11648/j.sjac.20150306.18</a>
Publisher
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Science Publishing Group
Date
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December 21, 2015
Language
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English
Type
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Journal Article
Identifier
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10.11648/j.sjac.20150306.18
2-Aminopyridine
Biofield Energy Treatment
Thermal Analysis
X-ray diffraction