Physicochemical Characterization of Biofield Energy Treated Calcium Carbonate Powder
Mahendra Kumar Trivedi1, Rama Mohan Tallapragada1, Alice Branton1, Dahryn Trivedi1, Gopal Nayak1, Omprakash Latiyal2, Rakesh Kumar Mishra2, Snehasis Jana2, *
1Trivedi Global Inc., Henderson, USA
2Trivedi Science Research Laboratory Pvt. Ltd., Bhopal, Madhya Pradesh, India
To cite this article:
Mahendra Kumar Trivedi, Rama Mohan Tallapragada, Alice Branton, Dahryn Trivedi, Gopal Nayak, Omprakash Latiyal, Rakesh Kumar Mishra, Snehasis Jana. Physicochemical Characterization of Biofield Energy Treated Calcium Carbonate Powder. American Journal of Health Research. Vol. 3, No. 6, 2015, pp. 368-375. doi: 10.11648/j.ajhr.20150306.19
Abstract: Calcium carbonate (CaCO3) is widely used in pharmaceutical industries and as a supplement in probiotics. The present study was designed to evaluate the effect of biofield energy treatment on the physicochemical properties of the CaCO3. The CaCO3 powder was divided into two parts and referred as control and treated. The control part was remained untreated, whereas treated part was subjected to Trivedi’s biofield treatment. The control and biofield treated samples were characterized using X-ray diffraction (XRD), particle size analyzer, surface area analyzer, thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FT-IR). The XRD showed that the crystallite size of treated CaCO3 was increased up to 100% as compared to the control. In addition, the lattice strain was reduced in treated sample as compared to the control. The particle size analysis result showed that the average particle size was significantly changed after treatment that led to considerably enhance the specific surface area of treated CaCO3 powder by 95% as compared to the control. The FT-IR spectroscopic analysis of the treated calcium carbonate showed shifting of wavenumber attributed to symmetric stretching vibrations of carbonate ion to higher wavenumber as compared to the control. The TGA analysis showed reduction in weight loss and increase in char yield which may be due to the increase in thermal stability of the treated sample. Therefore, the biofield treatment had significantly altered the physicochemical properties of the calcium carbonate. Hence, it is assumed that treated calcium carbonate could be used as a potential supplement of probiotics for food applications.
Keywords: Biofield Energy Treatment, Calcium Carbonate, Particle Size, Surface Area, FT-IR
The association of probiotics with wellbeing is established since time immemorial. Almost a century ago Henry Tissier reported that gut microbiota of healthy breast-fed infants were dominated by rod bifid (bifidobacteria) shaped bacteria which were absent in infants suffering from diarrhea, establishing the concept that they play a vital role to maintain human health . Thus probiotics are known as microorganisms which can confer good health to host when administered in adequate amount. It was reported that human gut contains 1014 bacterial cells which is 10 folds higher than the number of cells present in the human body [2-4]. The reported beneficial effect of probiotics consumption are improvement of intestinal health, alleviate the symptoms of lactose intolerance and minimize risk of other diseases [5,6]. Nevertheless, the imbalance of intestinal microbiota may cause health problems such as inflammatory bowel diseases, diarrhea, colon cancer, hypercholesterolemia, etc. . There are various probiotics based products that are available in the market. Yoghurt is perhaps the most common food  which is used to carry probiotics to the human gut. Additionally, some other products are used to carry probiotics are calcium, cheese, fermented milk, etc. Recently it was reported that calcium helps the bacteria to stick more properly to the intestinal wall. Specifically, calcium carbonate (CaCO3) is used commonly to lower the acid and to maintain the adherence of probiotics . Zhao et al. reported that addition of alkaline salts such as calcium carbonate in skimmed milk substantially increased the viable count of L. bulgaricus as compared to the control sample . Nevertheless, calcium carbonate has less solubility in water, hence it has less bioavailability in the human gastro intestinal tract. Tang et al. reported the increase in solubility of calcium when it was fermented with seven different strains of lactobacillus species . Therefore some novel methods should be devised to enhance the solubility i.e. bioavailability of calcium that can improve its food applications. Recently, biofield energy treatment has effectively modified the physicochemical properties of organic product , drugs , metal [14,15] and ceramic . Due to low solubility of CaCO3 and its application as supplement in probiotics, authors wish to investigate the influence of biofield energy treatment on CaCO3.
The National Center for Complementary and Alternative Medicine (NCCAM), a part of the National Institute of Health (NIH), recommends the use of Complementary and Alternative Medicine (CAM) therapies as an alternative to the healthcare sector and about 36% of Americans regularly uses some form of CAM . CAM includes numerous energy-healing therapies; biofield therapy is one of the energy medicine used worldwide to improve the health .
Willem Einthoven had developed electrocardiography (ECG) to measure the biofield of human body. Afterward, the Harold Saton Burr, had investigated the correlation of electric current with human body. Thus, human has the ability to harness the energy from environment/Universe and can transmit into any object (living or non-living) around the Globe. The object(s) always receive the energy and responding in a useful manner that is called biofield energy. This process is known as biofield energy treatment. Mr. Trivedi‘s biofield energy treatment (The Trivedi Effect®) has known to modify the physical, atomic, and thermal characteristics of various things associated with several scientific fields such as microbiology , and agriculture .
By conceiving the above-mentioned potential of biofield energy treatment and excellent properties of calcium carbonate, this study was conducted to investigate the impact of biofield energy treatment on the physicochemical properties of calcium carbonate nanopowder.
2. Materials and Methods
The CaCO3 powder used in this experiment was procured from the Sigma-Aldrich. The sample was divided into two parts; one was kept as a control sample while other was subjected to Trivedi’s unique biofield energy treatment and coded as treated sample. The treated group was in sealed pack and handed over to Trivedi for biofield energy treatment under standard laboratory conditions. Trivedi provided the energy treatment through his energy transmission process to the treated group without touching the sample. The control and treated samples were characterized by using X-ray diffraction (XRD), particle size analyzer, surface area analyzer, thermogravimetric analysis and Fourier transform infrared spectroscopy (FT-IR).
2.1. X-ray Diffraction (XRD) Study
The XRD analysis of control and treated CaCO3 were carried out on Phillips, Holland PW 1710 X-ray diffractometer system, which had a copper anode with nickel filter. The radiation of wavelength used by the XRD system was 1.54056 Å. The data obtained from this XRD were in the form of a chart of 2θ vs. intensity and a detailed table containing peak intensity counts, d value (Å), peak width (θ°), relative intensity (%) etc. The average crystallite size (G) was calculated by using formula:
G = kλ/(bCosθ) (1)
Here, λ is the wavelength of radiation used, b is full width half-maximum (FWHM) of peaks and k is the equipment constant (=0.94). Percentage change in average crystallite size was calculated using following formula:
Percent change in average crystallite size = [(Gt-Gc)/Gc] ×100 (2)
where, Gc and Gt are the average crystallite size of control and treated powder samples, respectively.
2.2. Particle Size Analysis
For particle size analysis, Laser particle size analyzer, Sympatec HELOS-BF was used, which had a detection range of 0⋅1–875 μm. The data obtained from the instrument was in the form of a chart of cumulative percentage vs. particle size, along with a detail table containing the size and percentage of the particle present. The data obtained from four treated samples were compared with the control. The percentage change in average particle size d50 and d99 (size below which 99% of the particles were present) were calculated as:
Percent change in particle size d50 (%) = [(d50_t - d50_c)/d50_c] x100 (3)
Here, d50_t and d50_c were the average particle size d50 of treated and control samples respectively. Similarly the percent change in d99 was also calculated and presented.
2.3. Surface Area Analysis
The surface area was measured by the Surface area analyzer, SMART SORB 90 based on Brunauer–Emmett–Teller (BET), which had a detection range of 0.2–1000 m2/g. The percent change in surface area was calculated as:
Percent change in surface area (%) = [(S_t - S_C)/S_C] x100 (4)
Here S_t and S_C were the surface area of treated and control samples, respectively.
2.4. Thermogravimetric Analysis-Differential Thermal Analysis (TGA-DTA)
The thermal stability of control and treated calcium carbonate were analyzed by using Mettler Toledo simultaneous TGA and Differential thermal analyzer (DTA). The samples were heated from room temperature to 400ºC with a heating rate of 5ºC/min under air atmosphere.
2.5. FT-IR Spectroscopy
For FT-IR analysis, Perkin Elmer, USA Fourier Transform Infrared (FT-IR) Spectrometer with frequency range of 300-4000 cm-1 was used.
3. Result and Discussion
3.1. X-ray Diffraction (XRD) Study
XRD is a non-destructive and quantitative technique, which has been extensively used to study the crystal structure parameters of any compound. The XRD diffractogram of control and treated CaCO3 samples were presented in Fig. 1. The XRD peaks observed in control and treated sample were well matched with the reported value in Joint committee on powder diffraction Standards (JCPDS) card number 88-1807 for CaCO3 powder . The most intense peak was observed at Bragg angle (2θ) 29.15° in control; however it was found at 29.20°, 29.33°, 28.92°, and 29.01° in the treated samples T1, T2, T3 and T4, respectively. This peak was corresponding to the crystalline plane (104) in control and treated samples. Moreover, the lattice strain along this plane was calculated using following equation:
It indicated that the crystallite size was significantly increased by 100.0, 14.3, 59.9, and 14.3% in T1, T2, T3 and T4, respectively as compared to the control (Fig. 2). Also, the inverse trend was observed in crystallite size and lattice strain. It was reported that the increase in temperature of CaCO3 leads to increase the crystallite size and decrease the lattice strain . It is possible that the reduction in lattice strain might cause the re-orientation of the neighboring planes in the same crystalline plane and that may results into higher crystallite size in treated sample as compared to control.
|Crystallite size (nm)||53.4||106.9||61.1||85.5||61.1|
|Lattice strain (x10-3)||2.68||1.34||2.33||1.69||2.36|
3.2. Particle Size Analysis
The particle size of control and treated CaCO3 samples are presented in Table 2. The data showed that average particle size (d50) was 48.2 μm in control and it was reduced to 43.4, 41.3, and 41.3 μm in T2, T3 and T4. However, it was slightly increased to 48.8 μm in the treated T1 sample. It indicates that d50 was significantly reduced by 10, 14.3, and 14.3% in T2, T3, and T4, respectively as compared to the control (Fig 3). In addition, particle size d99 (size below which 99% particles are present) was found as 101.2, 121.2, 109.4, 101.2, and 102.6 μm in control, T1, T2, T3, and T4 respectively. It indicated that d99 was increased by 19.8, 8.1, and 1.4% in T1, T2, and T4, respectively as compared to the control. Besides, based on reduction of d50 in T2, T3, and T4, through it was not changed in T3. It is assumed that the treated particles might be fractured and broken into finer particles as compared to the control.
However, to break the particles, a sufficient amount of stress energy is required and that depends upon the size and the type of material [23,24]. Typically, the CaCO3 powder exists as primary particles, which linked to each other through solid bonding. Muller et al. reported that stress energy required to breaking down the primary particles is much higher than the aggregates and agglomerates . It is possible that the energy, which probably transferred through biofield treatment induce the milling in treated CaCO3 sample. Nevertheless, the particle size d99 was enlarged in most of the treated samples, which was contrary to the reduction of d50 after treatment. It is assumed that cold welding and agglomeration process took place in treated CaCO3 samples . Further, the effect of change in particle size through biofield energy treatment on surface area was examined.
|Surface area (m2/g)||0.30||0.58||0.44||0.43||ND|
ND: Not detected
3.3. Surface Area Analysis
The specific surface area analysis of control and treated samples are illustrated in Table 2. It was observed that the surface area was increased from 0.30 m2/g (control) to 0.58, 0.44, and 0.43 m2/g in T1, T2, and T3, respectively. It indicates that the surface area was significantly increased by 95%, 50% and 45% in T1, T2 and T3, respectively as compared to the control (Fig. 4).
The increase of surface area of treated CaCO3 samples T2 and T3 could be due to decrease in particle size. However, the increase of surface area and the particle size in treated sample (T1) was quite unexpected, since both parameter are inversely proportional to each other i.e. the smaller the particles size, larger the surface area and vice versa. Thus, based on this, treated samples T2 and T3 were supported by the particle size result. Besides, the surface area of CaCO3 play an important role in controlling the bioavailability in human body. Noyes-Whitney proposed the relationship between rate of dissolution (R) and surface area (S) of a solid as following :
Where, D is diffusion constant, Cs and C are the concentration in the bulk dissolution medium and diffusion layer surrounding the solid, respectively, L is diffusion layer thickness. The equation suggested that the rate of dissolution of a compound can be modified through altering the surface area. The bioavailability of calcium from food is an important concern because calcium intake in our food is low and most of the calcium available in food is chemically bonded to other dietary constituents and must be released in a soluble form [28-30]. Hence, in this regard, the significant increase of surface area in treated CaCO3 could increase the rate of dissolution in human gastro intestinal tract. Thus, the higher dissolution of treated CaCO3 in the human gastric fluid, make it easily available for absorption in the body and that may lead to increase the bioavailability of the treated CaCO3 as compared to the control. It is assumed that high dissolution of calcium carbonate might improve its potential as probiotic supplement for food applications.
3.4. FT-IR Spectroscopy
The FT-IR spectra of control and treated CaCO3 samples are shown in Fig. 5. The spectra showed the absorption peak 713, 711, and 711 cm-1 in control, T1 and T2, respectively, which were attributed to in-plane bending of carbonate ion. The absorption peak observed at 873, 875, and 875 cm-1 in control, T1 and T2, respectively were ascribed to out-of-plane bending vibration of carbonate ion. Furthermore, the peak found at 1012, 1087, and 1095 cm-1 in the control, T1 and T2, respectively, were assigned to symmetric stretching of carbonate ions. In addition, the peak due to asymmetric stretching of carbonate ions were observed at 1450, 1448, and 1450 cm-1 in the control, T1 and T2, respectively. Thus, data suggested that that the absorption peak corresponding to symmetric stretching carbonate ion in the treated CaCO3 was shifted to higher frequency in T1 as compared to the control i.e. 1012→1095 cm-1.
In addition, the peak attributing to asymmetric stretching of carbonate ions was shifted to higher wave number in T1 as compared to the control i.e. 1450 →1448 cm-1. Based on the alteration in absorption wavenumber in T1 and T2, it is assumed that the biofield treatment might alter the bond force constant in the treated calcium carbonate.
3.5. TGA Analysis
TGA thermogram of control and treated calcium carbonate is presented in Fig. 6. TGA thermogram of control calcium carbonate showed an onset temperature at 533ºC and the endset temperature at 700 ºC. In this process, CaCO3 powder was decomposed to carbon dioxide (CO2) and calcium oxide (CaO). However, the thermogram of treated calcium carbonate showed similar thermal nature. The treated sample showed onset of thermal degradation at around 500ºC and the end set of thermal degradation was noticed at around 700ºC. The percentage weight loss of the control and treated calcium carbonate was 43.20% and 39.23%, respectively. Additionally, the residual char yield of the control and treated calcium carbonate was 2.92 and 3.36 mg, respectively. Hence, the result showed reduction in weight loss and increase in residual char yield of treated sample which indicated the increase in thermal stability of the treated sample as compared to the control.
In summary, the biofield energy treatment has significantly altered the crystallite size, particle size, and surface area of the calcium carbonate powder. The crystallite size was increased upto 100% in treated sample as compared to the control. In addition, the biofield energy treatment has significantly reduced the average particle size upto 14.3% as compared to the control. Furthermore, the surface area was significantly enhanced by 95% in treated sample as compared to the control. It indicated that the rate of dissolution of calcium carbonate in human gastric fluid might increase after biofield energy treatment. Therefore, it is assumed that the novel treated calcium carbonated with high surface area could make it a potential candidate as supplement for the probiotics food applications.
XRD: X-ray diffraction; TGA: Thermogravimetric analysis; FT-IR-Fourier Transform spectroscopy; Complementary and Alternative Medicine (CAM)
The authors would like to thank all the laboratory staff of MGV Pharmacy College, Nashik for their assistance during the various instrument characterizations. The authors would also like to thank Trivedi Science, Trivedi Master Wellness and Trivedi Testimonials for their support during the work.