Effect Of Deactivation Research Articles

Effects of nickel-deactivations on zeolites-Y of different SiO2/Al2O3 ratios in catalytic cracking of hydrocarbons

Effects of nickel deactivation on catalytic activities of three types of zeolites-Y (Y-5.1, USY-5.2, and VUSY-12) with varying SiO2/Al2O3 ratios were studied in cracking of hydrocarbons. Physicochemical characteristics such as crystalline phases, Ni oxidation states, morphology, acidity, surface area, and thermal stability of the samples were analysed. XRD revealed the absence of observable nickel compounds below 5 wt%, with NiO phase emerging at higher concentrations. Surface areas decreased from 826 to 615 m2/g (Y-5.1), 786–686 m2/g (USY-5.2), and 762–571 m2/g (VUSY-12) at 30 wt% Ni. The total acid sites also reduced from 17.247 to 9.826 µmol/g (Y-5.1), 15.464–8.854 µmol/g (USY-5.2), and 7.094–4.876 µmol/g (VUSY-12). XPS confirmed Ni2+ states. Catalytic cracking tests using n-Heptane demonstrated increases in C5-C6 alkanes, olefins, hydrogen, and methane yields as nickel concentration increased, with respective values of 64 %, 28 %, 79 % and 68 % for Y-5.1; 62 %, 28 %, 76 %, and 62 % for USY-5.2; and 58 %, 21 %, 75 %, and 60 % for VUSY-12. A corresponding decrease in heavier components were observed. The study demonstrates that nickel modification significantly impacts the physicochemical properties and catalytic performance of zeolite-Y and these depend strongly on the SiO2/Al2O3 ratios. The study gives further insights into the structural and catalytic modifications induced by nickel doping in zeolites, highlighting the potential of nickel-modified zeolites in promoting undesirable hydrogen and gas.

Design of green DES-based aqueous two phase systems for lipolytic enzymes extraction

This study pioneers a novel green and cost-effective separation process using reline deep eutectic solvent (DES) for extracting Thermomyces lanuginosus lipase (TlL) from aqueous solutions. For the first time, it has been shown that various potassium organic salts combined with reline DES can induce phase separation in aqueous solutions of the biodegradable non-ionic surfactant Tergitol 15-S9, presenting a groundbreaking alternative to the banned surfactant Triton X-100. This work uniquely applies three different equations to describe the experimental solubility curves. The selection of reline DES is particularly innovative as it avoids significant deactivation effects with three commercial lipases: Candida antarctica lipases A and B, and TlL, with the latter undergoing a detailed study. This includes an unprecedented analysis of its thermodeactivation kinetics in reline DES aqueous solutions. Additionally, a novel investigation of immiscibility regions at different temperatures, involving comprehensive Tie-Line characterizations (slope and length), preceded the evaluation of lipase extraction. Remarkably, the study demonstrates that optimizing the feed composition to contain higher water concentrations can achieve exceptionally high extraction efficiencies (approximately 90%), suggesting a transformative potential for future applications in real aqueous cultures.

What sizes of droplets contribute to long-range airborne transmission?

The size range of respiratory droplets contributing to long-range airborne transmission of infections determines the targeted intervention methods. However, the exact size range remains unknown, and the influencing parameters are also undetermined. Here, we investigated the size-resolved transport and fate of respiratory droplets in four reported venues of COVID-19 outbreaks. We utilised a transient number balance model, a set of expired droplet size distributions, existing formulas for size-resolved settling rates and filtration efficiencies, and a deposition model from the International Commission on Radiological Protection. This enabled us to obtain the size-resolved concentrations of exhaled droplets in indoor air, the size-resolved number of droplet nuclei in the inhaled air, and the number of droplets deposited throughout the respiratory tract. The newly defined airborne transmission size range of expired droplets depends on the effective dilution flow rate of the infection venue under consideration. Three criteria were proposed for determining the sizes of droplets involved in long-range airborne transmission. The airborne transmission droplets typically featured an initial diameter of 0.1–4–6 µm, with an hourly volume generation rate of 0.38–0.42 nL/h per index case in the four venues. This newly estimated volume of airborne transmission droplets provides an essential input into the viral load method for estimating the infectious quanta generation rate. Practical significanceOur size-resolved estimation reveals that only a tiny fraction of expired infectious droplets within an airborne transmission size range survives after the removal effects of ventilation, settling, deactivation, and filtration, as well as the transient dilution effect. These droplets remain in indoor air, potentially contributing to long-range airborne transmission. The airborne transmission size range depends on the size-dependent dilution capacity of a room.

Unveiling the influence of poisonous metals on NH3-SCR performance over NbOPO4 supported Cu-Ce catalyst

In this study, the underlying influence mechanism of different metal species, including K, Ca and Cd, on NbOPO4 supported Cu-Ce catalysts had been disclosed. Experimental results indicated that various metal species exhibited deactivating effect on SCR activities, where the deactivation effect decreased in the order of K > Ca ≈ Cd. Inherently, the pronounced decrease in SCR performances should be derived from the greatly deteriorated physicochemical properties, where various metal species deposited on CCP catalyst significantly suppressed redox ability and surface acidity and decreased surface area. However, compared with traditional V-W-Ti catalyst, NbOPO4 supported Cu-Ce catalyst still possessed superior resistance to different metal species.

Deactivation effect of elemental mercury oxidation over a V2O5-WO3/TiO2 catalyst by Pb in simulated coal-fired flue gas

Lead (Pb) is a typical heavy metal in the flue gas of coal-fired power plants, which can cause the deactivation of SCR catalysts. In this study, Pb-doped vanadium-based catalysts were prepared and investigated for the deactivation effect and mechanism of elemental Hg oxidation caused by Pb. The results showed that doping Pb on vanadium-based catalysts led to severe deactivation, which was more pronounced with increased Pb content. Further investigation illustrated that the introduction of Pb not only weakened the BET surface properties of vanadium-based catalysts but also increased the aggregation of surface species on the catalysts. After Pb introduction, the adsorption capacity toward elemental Hg, proportion of highly oxidized V5+, and surface Oβ ratio significantly decreased severely weakening the activity of the catalyst. In addition, we demonstrated that the reaction between Pb and active VO/V−OH groups of the catalyst formed inactive V−O−Pb species, which was the direct cause of catalyst deactivation.

Enhanced oriented oxidation of medium and long chain alkanes by inactivating hydrophilic organics of soil organic matter

Aiming to explore the effect of deactivation of soil organic matter (SOM) on the oriented oxidation of n-alkanes, the petroleum-contaminated soil was pretreated with K2HPO4, and then the soil was treated with Fenton oxidation. After the soil was regulated by K2HPO4, the hydrophilic organics (Protein II and Humic acid-like) in SOM were deactivated, which made the ·OH transfer to oxidize TPH, to achieve efficient oriented oxidation of TPH. After the passivation of hydrophilic organics, the TPH oxidation amount of the efficient group was as high as 6007 mg/kg, which was 1.57 times than unregulated group. In efficient oriented oxidation group, the TPH oriented oxidation amount reached 2186 mg/kg, and the TPH oxidation amounts of unit hydroxyl strength reached 759.42 mg/kg, and the oxidation effect of the medium and long chain alkanes was improved. The results showed that 22.60 % ·OH was transferred to TPH, and the relative reactivity coefficient increased from 0.7 to 1.8(with k>1), which was the reason for improving the oriented oxidation effect of medium and long chain alkanes. It was also found that the two hydrophilic organics had high correlations with TPH oxidation (R2 = 0.9). Further analysis found that the passivation of hydrophilic organics was mainly through the reaction of PO43- with protein and humus in soil organic matter. In general, this study greatly reduced the ineffective consumption of ·OH by SOM, thereby improving the utilization efficiency of H2O2 and realizing the efficient oriented oxidation of petroleum hydrocarbons, which provided great reference value for practical engineering applications.

The temperature dependence of electrochemical CO2 reduction on Ag and CuAg alloys

Ag is often studied as catalyst for electrochemical CO2 reduction as it shows high selectivity towards CO and is easily alloyed with Cu to enhance performance using CuAg catalysts. In this study, we investigated the effect of temperature on Ag and CuAg catalysts and compare these with previous results on Au and Cu catalysts. We show that the temperature effect is complicated as it shows an interplay with CO2 concentration, potential and mass transport. It is therefore crucial to deconvolute these parameters and study the effect of temperature under different conditions. Moreover, we show that alloying Ag with Cu can inhibit some of the deactivation effects observed at high temperatures on pure Cu. CuAg alloys can prevent the dominance of hydrogen evolution at elevated temperatures, although an optimum of C2+ products with temperature is still observed.

The Effect of NF-κB Deactivation on Cancer Cell Response to ALA Mediated Photodynamic Therapy.

Breast cancer is one of the most widespread tumors among women worldwide, which is difficult to treat due to the presence of chemoresistance and the risk of tumor recurrence and metastasis. There is a pressing necessity to develop efficient treatments to improve response for treatment and increase prolong survival of breast cancer patients. Photodynamic therapy (PDT) has attracted interest for its features as a noninvasive and relatively selective cancer treatment. This method relies on light-activated photosensitizers that, upon absorbing light, generate reactive oxygen species (ROS) with powerful cell-killing outcomes. Nuclear factor kappa B (NF-κB), a transcription factor, plays a key role in cancer development by regulating cell proliferation, differentiation, and survival. Inhibiting NF-κB can sensitize tumor cells to chemotherapeutic agents. Dimethyl fumarate (DMF), an NF-κB inhibitor approved by the FDA for multiple sclerosis treatment, has further shown promise in suppressing breast cancer cell growth in vitro. We hypothesized that combining PDT with Dimethyl fumarate (DMF) could further enhance therapeutic efficacy for both treatment modalities. In the current study, we explored the PDT effect of 1 and 2 mM aminolaevulinic acid (ALA) and low-power He-Ne laser irradiation combined with different concentrations of DMF (2.5, 1.25, or 0.652 µg/ml) against hormone nonresponsive AMJ13 breast cancer cell line that is derived from Iraqi patient. Our results demonstrated that co-administration with all tested DMF concentrations significantly enhanced the cytotoxicity of PDT antitumor effect. The combination index analysis showed presence of synergism in combining PDT with DMF. This finding suggests that the combination of PDT with DMF could be a promising novel strategy against triple negative breast cancer that could be applied clinically due to the fact that both of these treatments are already clinically approved therapies.

Noble metal (Pt, Pd and Rh) promoted Ni-Co/Mg(Al)O catalysts for steam reforming of tar impurities from biomass gasification

Steam reforming is a promising approach to remove biomass gasification tar impurities. Noble metal promotion (Pt/Pd/Rh), Ni+Co loading (20–40 wt%) and calcination temperature (600–800 °C) effects were investigated with hydrotalcite-derived Ni-Co/Mg(Al)O catalysts for bio-syngas tar steam reforming. Fresh catalysts were characterized by XRD, ICP-MS, XRF, N2-physisorption, H2-chemisorption and TPR. Small-diameter metal particles were achieved (5.1–5.8 nm) below a Ni+Co loading threshold (above 30 wt%). Model bio-syngas activity tests were performed (CH4/H2/CO/CO2 molar ratio = 10/35/25/25, 700 °C, steam-to-carbon = 3.0) with and without tar addition (toluene/1-methylenaphthalene, 10 g/Nm3). Tar elimination was achieved with all samples. Enhanced reforming activity accompanied by strong tar active site inhibition effects were found for the Rh promoted catalyst. Noble metal promoted samples were effectively reduced in the bio-syngas environment (H2/CO/CH4) without any pre-reduction (in situ activation by the action of the syngas) with Rh > Pt > Pd. Coke characterization was conducted with TPO-MS and Raman spectroscopy. High-dispersion 20NiCo/30NiCo samples were strongly deactivated through active site inhibition and coke formation. High-temperature calcination (800 °C) reduced the deactivation effects of the coke deposition, attributed to enhanced Mg(Al)O-assisted coke gasification.

E. Coli inactivation by humidified air barrier discharge plasmas and the chemical stability of amino acids

In this study, we use atmospheric air dielectric barrier discharge (DBD) plasma to inactivate E. coli (E. coli) by changing the air humidity levels. In order to analyze the inactivation process of E. coli during the humidified air DBD plasma treatment, we analyze the byproducts of 12 representational amino acids and compare their chemical stability. The experimental results show that the E. coli surface density (CFU cm−2) on a steel disc decreased significantly when the air humidity was increased from 20% to 60%, and humidified air DBD plasma at 60% humidity is very effective in inactivating E. coli. A consistently potent deactivation effect on E. coli can be seen in plasma afterglow treatment experiments over a storage time of two minutes, indicating that plasma-activated long-lived reactive oxygen and nitrogen species play a crucial role in controlling the E. coli inactivation. Compared to the low humidity (20%) condition, the concentration of reactive species produced by the plasma at high humidity (60%) increased 2-fold for 2-hydroxyterephthalic acid and 5-fold for hydrogen peroxide while ozone production was halved. Amino acid experiments showed that amino acids may be oxidized, hydroxylated and nitroxylated by reactive species. The reduction of amino acids by air DBD plasma was even more pronounced at high air humidity compared to low air humidity. Our analysis indicates that the significant inactivation of E. coli by humified air DBD plasma is related to the chemical instability of amino acids.

Kinetically Inert Platinum (II) Complexes for Improving Anticancer Therapy: Recent Developments and Road Ahead.

The search for better chemotherapeutic drugs to alleviate the deficiencies of existing platinum (Pt) drugs has picked up the pace in the millennium. There has been a disparate effort to design better and safer Pt drugs to deal with the problems of deactivation, Pt resistance and toxic side effects of clinical Pt drugs. In this review, we have discussed the potential of kinetically inert Pt complexes as an emerging class of next-generation Pt drugs. The introduction gives an overview about the development, use, mechanism of action and side effects of clinical Pt drugs as well as the various approaches to improve some of their pharmacological properties. We then describe the impact of kinetic lability on the pharmacology of functional Pt drugs including deactivation, antitumor efficacy, toxicity and resistance. Following a brief overview of numerous pharmacological advantages that a non-functional kinetically inert Pt complex can offer; we discussed structurally different classes of kinetically inert Pt (II) complexes highlighting their unique pharmacological features.

The effects of Facebook and Instagram on the 2020 election: A deactivation experiment

We study the effect of Facebook and Instagram access on political beliefs, attitudes, and behavior by randomizing a subset of 19,857 Facebook users and 15,585 Instagram users to deactivate their accounts for 6 wk before the 2020 U.S. election. We report four key findings. First, both Facebook and Instagram deactivation reduced an index of political participation (driven mainly by reduced participation online). Second, Facebook deactivation had no significant effect on an index of knowledge, but secondary analyses suggest that it reduced knowledge of general news while possibly also decreasing belief in misinformation circulating online. Third, Facebook deactivation may have reduced self-reported net votes for Trump, though this effect does not meet our preregistered significance threshold. Finally, the effects of both Facebook and Instagram deactivation on affective and issue polarization, perceived legitimacy of the election, candidate favorability, and voter turnout were all precisely estimated and close to zero.

Structural Changes of Ni and Ni-Pt Methane Steam Reforming Catalysts During Activation, Reaction, and Deactivation Under Dynamic Reaction Conditions.

Ni-based catalysts are the most widely used materials to produce H2 in large-scale methane steam reformers under stationary conditions. For domestic applications such as fuel cells, H2 production involves the exposure of the catalysts to more dynamic conditions due to the daily startup and shutdown operation mode, making Ni-based catalysts susceptible to oxidation and deactivation. In this context, we report a systematic investigation of the structural changes occurring for monometallic Ni/MgAlOx and bimetallic NiPt/MgAlOx catalysts during methane steam reforming under transient conditions, comprising catalyst activation, operation, and deactivation processes. Besides extensive catalytic tests, the samples prepared by incipient wetness impregnation were characterized by complementary methods, including N2-physisorption, X-ray diffraction, H2-temperature-programmed reduction, and electron microscopy. Next, the structure of the Ni and Pt species was monitored under reaction conditions using time and spatially resolved in situ/operando X-ray absorption spectroscopy. The results obtained show that before catalyst activation by H2-reduction, nickel diffuses into the support lattice and forms mixed oxides with magnesium. In the activated catalysts, Ni is present in the metallic state or alloyed with Pt. A clear beneficial effect of the noble metal addition was identified on both the activity and stability of the bimetallic NiPt/MgAlOx catalyst. In contrast, the pronounced oxidation and reincorporation of Ni into the support lattice were observed for the monometallic sample, and these catalyst deactivation effects are hindered in the bimetallic Ni-Pt catalyst. Overall, the outcome of our study not only helps in understanding the catalyst activation/deactivation processes at an atomic level but also provides the basis for the rational development of improved methane steam reforming catalysts.

Electromagnetic Nature of Distant Interaction of the Atmospheric Pressure Helium Plasma Discharge Tube with Glioblastoma Cancer Cells.

Atmospheric pressure coaxial gaseous discharge tubes (DTs) with helium have demonstrated potential for in vitro inactivation or sensitization of glioblastoma cancer cells. Here, we study the effect of two configurations of the DT electrode system on its electromagnetic emissivity as well as other physical factors (heating and UV emission) that form in the vicinity of this device. We demonstrate that the configuration of the DT electrodes that concentrates the discharge streamers near the top of the device has a distant (cm scale) deactivation effect on U87-MG glioblastoma cancer cells when irradiated, without measurable UV components in the DT optical emission spectra. This effect persists even through different barriers such as glass, plastic, or quartz Petri dishes but is eliminated when glass or plastic dishes are filled with water. These findings demonstrate the potential for development of noninvasive, physical-based treatment methods of deep-tissue tumors.

Entrained-flow pyrolysis and (co-)gasification characteristics of Indian high-ash coals

Co-utilization in entrained-flow gasifiers is a potential solution to address the high ash-related problems persistent in fluidized-bed gasifiers. This work presents the hitherto unreported high-temperature (1000–1400 °C) entrained-flow pyrolysis and (co-) gasification characteristics of Indian high-ash coals and two candidate fuels (indigenous bituminous coal and petcoke) for possible co-utilization. Char analyses – TGA, FTIR, Raman, and SEM − are also performed to characterize the pyrolysis-induced structural changes. Volatile yields of candidate fuels matched with proximate values while those of high-ash coal exceeded by ∼12 wt%. Thermal deactivation was more pronounced for coal chars. High-ash coals achieved 100% carbon conversion at conditions exceeding 1300 °C and 20 vol% CO2. Bituminous coal showed comparable conversions, 70−90%, at identical conditions; further increase in conversion potential may be possible through steam addition due to enhanced char deactivation and pore diffusion effects at higher temperatures. Petcoke achieved lowest conversion of ∼30% even at the severest conditions; decreasing the average particle size by half showed an improvement of only ∼15%. Co-gasification of high-ash coal and petcoke blends showed no synergy. Considering closely matching carbon conversion, volatile release potential, and industry-standard slag tapping temperatures (1300−1500 °C), indigenous bituminous coals are more promising for co-utilization with high-ash coals in autothermal entrained-flow gasifiers.

Perylene diimide covalent organic frameworks super-reductant for visible light-driven reduction of aryl halides

In recent years, there has been a growing interest in the utilization of molecular photocatalysts in their radical ionic forms, especially as visible-light super-reductants. These catalysts exhibit remarkable capabilities in facilitating otherwise inert high-potential organic reactions, such as the reduction of aryl halides to aryl radicals. However, the development of heterogeneous super-reductants has lagged behind due to the deactivation effect caused by molecular aggregation. This study presents a novel approach to address this limitation by heterogenizing perylene diimides (PDIs) super-reductants with a consecutive photo-induced electron transfer mechanism into two-dimensional donor-acceptor (D-A) covalent organic frameworks (COFs). Both COFs, possessing D-A electronic structures and photothermal effects, demonstrated superior visible-light photocatalytic performance compared to their homogeneous counterparts. They achieved up to 99% conversion in the dehalogenation of aryl halides, primarily through a hydrogen atom trapping aryl radical mechanism. Additionally, we conducted a comparative investigation of the excited states of radical anionic D-A-type COFs and DPPDI using femtosecond transient absorption spectroscopy. Notably, the lifetimes of COFs were significantly prolonged, measuring 210 and 260 ps, respectively, compared to the 150 ps lifetime of (DPPDI•−). This study offers valuable insights into the design of efficient free radical ion-type photocatalysts, with potential applications in various chemical transformations.

Experimental assessment of low temperature plasma devices for bacterial aerosol inactivation in the air duct of HVAC systems.

In light of growing concerns about indoor air quality and the transmission of pathogens, this study aims to evaluate the effectiveness of low temperature plasma (LTP) devices in inactivating bacterial aerosols in the air duct of HVAC systems, exploring methods to enhance air purification efficiency. This research employed experimental methods to explore the deactivation effects of LTP on common bacteria such as E. coli and Bacillus subtilis, focusing on the role of air parameters such as the airflow rate, relative humidity, and temperature in influencing the device's performance. Notably, the study determined that an operational voltage of 3000 V for the LTP device, combined with conditions of low airflow, low humidity, and high temperature, significantly enhances the inactivation of bacterial aerosols, achieving an 82% inactivation rate at a negative ion concentration of 2.4 × 1011 ions per m3 and a wind speed of 3 m s-1. Despite the generation of ozone and ultraviolet light as by-products, their concentrations were found to be within safe limits for human exposure. In addition, this study identified an effective inactivation range, alongside an optimal arrangement for the airflow direction within ducts, to maximize the sterilization efficiency of the LTP device. Given these promising results, the study advocates for the integration of LTP technology into the air duct of HVAC systems of public buildings to improve air quality and reduce the risk of airborne disease transmission.

Unexpected offsetting effect of Na and HCl deactivation over CeO2-MoO3 catalyst for NO reduction

This work mainly illustrated the synergistic effects of Na and HCl on the SCR performance of CeMo catalysts. Given that the fresh CeMo catalyst was treated with HCl or doped by Na, the weakened acidity and oxidizability would interfere with the adsorption and activation of NH3, thus resulting in a downward trend of the catalyst deNOx performance. Notably, for the HCl treated Na-poisoned catalyst, the treatment with HCl introduced additional acid sites onto the Na-poisoned catalyst surface and increased the availability of Ce4+ and chemisorbed oxygen. These behaviors exerted a certain promotional effect on the adsorption and activation of NH3. Apparently, the catalyst's deNOx performance slightly rebounded, suggesting the offsetting effects of HCl. Such knowledge would be vital to the stable operation in real coal-fired flue gas.

Selective Synergistic Catalytic Elimination of NOx and CH3SH via Engineering Deep Oxidation Sites against Toxic Byproducts Formation.

NOx and CH3SH as two typical air pollutants widely coexist in various energy and industrial processes; hence, it is urgent to develop highly efficient catalysts to synergistically eliminate NOx and CH3SH. However, the catalytic system for synergistically eliminating NOx and CH3SH is seldom investigated to date. Meanwhile, the deactivation effects of CH3SH on catalysts and the formation mechanism of toxic byproducts emitted from the synergistic catalytic elimination reaction are still vague. Herein, selective synergistic catalytic elimination (SSCE) of NOx and CH3SH via engineering deep oxidation sites over Cu-modified Nb-Fe composite oxides supported on TiO2 catalyst against toxic CO and HCN byproducts formation has been originally demonstrated. Various spectroscopic and microscopic characterizations demonstrate that the sufficient chemisorbed oxygen species induced by the persistent electron transfer from Nb-Fe composite oxides to copper oxides can deeply oxidize HCOOH to CO2 for avoiding highly toxic byproducts formation. This work is of significance in designing superior catalysts employed in more complex working conditions and sheds light on the progress in the SSCE of NOx and sulfur-containing volatile organic compounds.

Monitoring the neural activity associated with praying in Sahaja Yoga meditation.

Sahaja Yoga Meditation draws on many religious traditions and uses a variety of techniques including Christian prayer to reach a state known as thoughtless awareness, or mental silence. While there are many studies on the neural correlates of meditation, few studies have focused on the neural correlates of praying. Thus, the aim of our research was to study the neural activity associated with the prayer practices in Sahaja Yoga Mediation, which have not been studied before, to explore effects beyond repetitive speech or "mantra effects". Sixteen experienced Sahaja Yoga Meditation practitioners were scanned using task based functional Magnetic Resonance Imaging while performing formalised and improvised forms of praying and their equivalent secular tasks. Our results showed the deactivation of bilateral thalamus during both prayers compared to secular conditions and the activation in the medial prefrontal cortex that was reduced by religious and formalised secular speech conditions but increased during improvised secular speech; similarly, frontal regions were deactivated when comparing prayers to their secular equivalents. These results seem to depict two important factors related with praying in Sahaja Yoga Meditation merging inner concentration and social cognition. First, the perception of the surroundings mediated by the thalamus may be decreased during these prayers probably due to the establishment of inner concentration and, second, frontal deactivation effects could be related to reduced social judgement and 'mentalizing', particularly in the medial prefrontal cortex. Our findings suggest that praying by Sahaja Yoga Meditation practitioners is neurophenomenologically different from the social cognitive attempt of praying within Christian praying practices.