Assessment of NORMs (238U, 232Th, 40K) and radiation hazard indices in Beldih apatite mine region of Purulia district, West Bengal, India.

The radiation arising from naturally occurring radioactive materials (NORMs) is the foremost contributor to the collective dose received by the global population. The present study aims to measure the natural background radiation level and the associated gamma radiation dose in air in the Beldih apatite mine region of Purulia district, India. This study is primarily focused on the determination of 238U, 232Th and 40K activities in the sub-surface soil of the study area. The measurements were carried out using a High Purity Germanium (HPGe) detector-based gamma-ray spectrometer with a relative efficiency of 80%. To achieve uniformity in exposure estimations, radium equivalent activity has been calculated. Additionally, the internal hazard index, external hazard index, radioactivity level index and gamma dose rates have been evaluated to estimate the radiation hazard levels in the study area. The comparison of obtained concentrations and hazard indices with global data (UNSCEAR. (2008). Sources, effects and risks of ionizing radiation. United nations scientific committee on the effects of atomic radiation (report to the general assembly, with Annexes).) suggests that this region lies in a relatively high background radiation zone.

Fe(III) cross-linked cellulose-agar hydrogel beads for efficient phosphate removal from aqueous solutions.

Fe(III) cross-linked cellulose agar beads (Fe-CLCAB) were synthesized by sol-gel method and employed as adsorbents for the removal of phosphate ions from aqueous medium. The synthesized Fe-CLCAB was characterized by its swelling property, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and UV-Vis absorption spectroscopic analysis. Batch adsorption studies were carried out to find out the optimum conditions of phosphate uptake. The adsorption process was found to fit both Langmuir and Freundlich adsorption isotherm model, pseudo-second-order kinetic model, and Elovich kinetic model. Ninety-four percent phosphate adsorption was achieved with 500 beads at pH 5. Maximum monolayer adsorption capacity was 73.13 mg/g. A two-step elution process using sodium chloride solution was suitable for complete desorption of phosphate from Fe-CLCAB. Six cyclic adsorption-desorption tests were conducted using a 0.1 M NaCl solution as desorbing agent. The removal efficiency of regenerated Fe-CLCAB was 42% of its original value after six cycles, which validates good stability and effectiveness of the prepared hydrogel beads. Ion exchange plays a vital role during adsorption/desorption of phosphate.

Estimation of gross α-ß and tritium activities in groundwater samples using LSC-TDCR technique in and around the geothermal region of Eastern India.

The present study is an attempt to assess the radiogenic quality of groundwater on the basis of gross α, gross ß and tritium (3H or H-3) activities in the Bakreswar-Tantloi geothermal region of Chotanagpur Plateau, West Bengal and Jharkhand, India. The aforesaid parameters in groundwater samples were measured using liquid scintillation counting triple to double coincidence ratio (LSC-TDCR) technique. Groundwater samples collected from Bakreswar-Tantloi geothermal region show gross α activities from below the minimum detectable activity (BMDA) to 0.5 ± 0.05 Bq/L, gross ß activities from BMDA to 0.2 ± 0.01 Bq/L and H-3 activities from BMDA to 63.42 Bq/L. The average gross α, gross ß and H-3 activities are also within the permissible limits prescribed by the World Health Organization (WHO). Though the annual effective doses in some samples were higher than the reference dose level of 0.1 mSv, the overall result suggests that the groundwater in the Bakreswar-Tantloi geothermal region is radiologically safe considering the radionuclides covered in this study.

Liquid-liquid extraction of No-carrier-added 129Cs with various extractants.

Two different iodide targets, BiI3 and KI were irradiated by α-particles to produce 129Cs via 127I(α, 2n)129Cs reaction. 129Cs was separated from bulk Bi (when BiI3 was used as target) by anion exchanger TOA dissolved in cyclohexane. Irradiation of KI with alpha particle produced 129Cs along with minute amount 44mSc. 44mSc was successfully separated from 129Cs using 18-crown 6 ether dissolved in nitrobenzene.

Studies on radiation stability of natural caffeine.

Behavior of isolated caffeine in 60Co- γ radiation environment was studied in solid form as well as in aqueous medium. No degradation in solid caffeine structure was observed after exposing up to a dose of 10 kGy. In aqueous medium, 98% radiolytic degradation of caffeine was observed after application of 1.26 kGy γ dose. Radiation chemical yield decreased with increasing dose. The degradation was mostly favored in neutral medium. Addition of ethanol decreased the radiolytic degradation efficiency.

Studies on production of 43,44,44mSc from 12C+natCl reactions up to 64 MeV projectile energy.

For the first-time production of 43,44,44mSc radionuclides via 12C + natCl reaction have been reported. Production yield and experimental cross sections of natCl(12C,xn)43,44,44mSc up to 64 MeV have been reported. Experimental cross sections have been found comparable with the theoretically evaluated data using PACE4 and EMPIRE3.2.2 codes.

Separation of 71,72As from alpha particle induced gallium oxide target by solid cation and anion exchangers, DOWEX-50 and DOWEX-1.

46.0 MeV alpha particle induced reaction on gallium oxide target results production of no-carrier-added (NCA) 71,72As and 67Ga tracer. 71,72As were separated from the target matrix by solid liquid extraction (SLX) using two different exchangers, Dowex-1 and Dowex-50. At best condition of 0.2 g Dowex-1 + 6 M HCl and 0.2 g Dowex-50 + 10-3 M HCl bulk gallium was completely extracted leaving behind NCA 71,72As in the aqueous phase. Dowex-50 was found to be more suitable and offered high separation factor, 3.2 × 105.

Theranostic Terbium Radioisotopes: Challenges in Production for Clinical Application.

Currently, research on terbium has gained a momentum owing to its four short-lived radioisotopes, 149Tb, 152Tb, 155Tb, and 161Tb, all of which can be considered in one or another field of nuclear medicine. The members of this emerging quadruplet family have appealing nuclear characteristics and have the potential to do justice to the proposed theory of theranostics nuclear medicine, which amalgamates therapeutic and diagnostic radioisotopes together. The main challenge for in vivo use of these radioisotopes is to produce them in sufficient quantity. This review discusses that, at present, neither light charged particle nor the heavy ion (HI) activation are suitable for large-scale production of neutron deficient terbium nuclides. Three technological factors like (i) enrichment of stable isotopes to a considerable level, (ii) non-availability of higher energies in commercial cyclotrons, and (iii) non-availability of the isotope separation technique coupled with commercial accelerators limit the large scale production of terbium radionuclides by light charged particle activation. If in future, the technology can overcome these hurdles, then the light charged particle activation of enriched targets would produce a high amount of useful terbium radionuclides. On the other hand, to date, the spallation reaction coupled with an online isotope separator has been found suitable for such a requirement, which has been adopted by the CERN MEDICIS programme. The therapeutic 161Tb radionuclide can be produced in a reactor by neutron bombardment on enriched 160Gd target to produce 161Gd which subsequently decays to 161Tb. The radiochemical separation is mandatory even if the ISOL technique is used to obtain high radioisotopic purity of the desired radioisotope.

Separation of 206Po from alpha particle irradiated lead bismuth eutectic target.

Lead bismuth eutectic (LBE) target was bombarded with 46 MeV α-particle. Possibility of separation of no-carrier-added (NCA) polonium radioisotopes from the bulk lead-bismuth eutectic target was explored. Differential precipitation showed presence of Po with bulk Bi, leaving behind bulk Pb in aqueous medium. NCA 206Po radioisotope was then separated from bulk Bi using trioctylamine (TOA) as the extractant. At best condition of 0.01 M TOA+0.1 M HCl, highest separation factor (>500) was achieved between NCA Po and bulk Bi.

Interaction of metal oxide nanoparticles with microplastics: Impact of weathering under riverine conditions.

The ubiquitous distribution of microplastics (MPs) leads to inevitable interactions with the toxic pollutants present in the environment including metal-oxide nanoparticles. This study investigates the interaction of CeO2 nanoparticles (CeNPs) with MPs generated from a disposable plastic container. Further, rough MPs (R-MPs), generated through mechanical abrasion of MPs with sand, were used to probe the impact of roughness. To understand the sorption kinetics and underlying interaction processes, batch experiments were carried out. The results distinctly indicate that CeNPs sorption occurred on MPs surfaces and was consistent with the pseudo-second order kinetics model. For pristine MPs, the sorption capacity was as high as 12.9 mg/g while for R-MPs kinetic equilibrium was achieved faster and an enhanced sorption capacity (13.4 mg/g) was identified. A rise in sorption with an increase in salinity was noted while pH and humic acid exhibited a negative correlation. The observed interactions were attributed to the aggregation profile and surface charge of CeNPs and MPs. Surprisingly, CeNPs also got loaded onto MPs in non-agitated and undisturbed conditions. The sorption process was influenced by the type of aqueous matrix and the sorption capacity at equilibrium followed the trend: distilled water> synthetic freshwater> river water. FTIR spectra, zeta potential, SEM imaging, and elemental mapping revealed electrostatic interaction as the dominant mechanism. This work contributes towards the knowledge gap on the environmental risk of MPs.

Fabrication of thiophene-chitosan hydrogel-trap for efficient immobilization of mercury (II) from aqueous environs.

The fabrication of thiophene-chitosan (TCS) hydrogel has been carried out to show the excellent binding performance of Hg(II) from an aqueous solution of heavy metal ions in presence of thiophene moiety within the hydrogel network. Thiophene moiety has been implanted within chitosan, a wild bio-resources, through a facile Schiff base condensation strategy with 2-thiophenecarboxaldehyde to develop a three-dimensional network of TCS hydrogel. The parameters influencing adsorption capacity such as pH, volume of functional agent, contact time, amount of the hydrogel are included to broaden the in-depth study for the adsorption window of Hg(II) followed by the desorption and reusability performance of TCS. The results indicate that the TCS hydrogel for Hg(II) followed pseudo-second-order kinetics. Ethylenediaminetetraacetic acid (EDTA), acts as a better eluent compared to HCl to desorb Hg(II) and even after recurring adsorption/desorption cycles, removal efficacy of TCS hydrogel could be retained.

Radiogenic quality assessment of ground and riverine water samples collected from Indian Sundarbans.

The present study attempts to generate the first baseline data on gross α and ß activities in groundwater and riverine water samples collected from different regions of Indian Sundarbans, a part of the world's largest mangrove ecosystem. Until the present, no information is available related to radioactivity measurement in water samples from this vast area. Gross alpha-beta activities were measured by liquid scintillation counting-triple to double coincidence ratio (LSC-TDCR) technique. The minimum detectable activities in present experimental condition were found to be 21 mBq L-1 and 55 mBq L-1 for gross α and ß respectively. Gross alpha activities in all groundwater and riverine samples were found to be below the detection limit (BDL), whereas gross beta activities in groundwater and riverine samples varied from BDL to 0.46 ± 0.24 Bq L-1 and BDL to 0.90 ± 0.26 Bq L-1 respectively, which are below WHO recommended value 1 Bq L-1. Annual effective doses were below 0.1 mSv. U and Th concentrations in the water samples were determined by ultrasonic-nebulizer assisted Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) and found to be BDL. For assessing 3H activity, double-distilled water samples were measured by LSC-TDCR technique, which provided BDL result.

A Tripartite Interaction among the Basidiomycete Rhodotorula mucilaginosa, N2-Fixing Endobacteria, and Rice Improves Plant Nitrogen Nutrition.

Nitrogen (N) limits crop yield, and improvement of N nutrition remains a key goal for crop research; one approach to improve N nutrition is identifying plant-interacting, N2-fixing microbes. Rhodotorula mucilaginosa JGTA-S1 is a basidiomycetous yeast endophyte of narrowleaf cattail (Typha angustifolia). JGTA-S1 could not convert nitrate or nitrite to ammonium but harbors diazotrophic (N2-fixing) endobacteria (Pseudomonas stutzeri) that allow JGTA-S1 to fix N2 and grow in a N-free environment; moreover, P. stutzeri dinitrogen reductase was transcribed in JGTA-S1 even under adequate N. Endobacteria-deficient JGTA-S1 had reduced fitness, which was restored by reintroducing P. stutzeri JGTA-S1 colonizes rice (Oryza sativa), significantly improving its growth, N content, and relative N-use efficiency. Endofungal P. stutzeri plays a significant role in increasing the biomass and ammonium content of rice treated with JGTA-S1; also, JGTA-S1 has better N2-fixing ability than free-living P. stutzeri and provides fixed N to the plant. Genes involved in N metabolism, N transporters, and NODULE INCEPTION-like transcription factors were upregulated in rice roots within 24 h of JGTA-S1 treatment. In association with rice, JGTA-S1 has a filamentous phase and P. stutzeri only penetrated filamentous JGTA-S1. Together, these results demonstrate an interkingdom interaction that improves rice N nutrition.

Author Correction: An Endophytic Bacterial Consortium modulates multiple strategies to improve Arsenic Phytoremediation Efficacy in Solanum nigrum.

A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has not been fixed in the paper.

An Endophytic Bacterial Consortium modulates multiple strategies to improve Arsenic Phytoremediation Efficacy in Solanum nigrum.

Endophytic microbes isolated from plants growing in contaminated habitats possess specialized properties that help their host detoxify the contaminant/s. The possibility of using microbe-assisted phytoremediation for the clean-up of Arsenic (As) contaminated soils of the Ganga-Brahmaputra delta of India, was explored using As-tolerant endophytic microbes from an As-tolerant plant Lantana camara collected from the contaminated site and an intermediate As-accumulator plant Solanum nigrum. Endophytes from L. camara established within S. nigrum as a surrogate host. The microbes most effectively improved plant growth besides increasing bioaccumulation and root-to-shoot transport of As when applied as a consortium. Better phosphate nutrition, photosynthetic performance, and elevated glutathione levels were observed in consortium-treated plants particularly under As-stress. The consortium maintained heightened ROS levels in the plant without any deleterious effect and concomitantly boosted distinct antioxidant defense mechanisms in the shoot and root of As-treated plants. Increased consortium-mediated As(V) to As(III) conversion appeared to be a crucial step in As-detoxification/translocation. Four aquaporins were differentially regulated by the endophytes and/or As. The most interesting finding was the strong upregulation of an MRP transporter in the root by the As + endophytes, which suggested a major alteration of As-detoxification/accumulation pattern upon endophyte treatment that improved As-phytoremediation.

Converter target chemistry - A new challenge to radioanalytical chemistry.

The 1-2 GeV proton induced spallation reaction on the high Z materials like Hg, or lead bismuth eutectic (LBE), popularly known as converter targets, will produce strong flux of fast neutrons which would further react with fissile materials to produce intense radioactive ion beam (RIB). LBE offers suitability for use as converters over Hg but it suffers from the demerit of radiotoxic polonium production. These targets may be viewed as a store house of clinically important and other exotic radionuclides. For application of those radionuclides, radiochemical separation from bulk target material is of utmost importance.

Separation of no-carrier-added astatine radionuclides from α-particle irradiated lead bismuth eutectic target: A classical method.

Possibility of separation of no-carrier-added (NCA) astatine radionuclides from the bulk lead-bismuth-eutectic (LBE) target was explored in a simple way in the laboratory scale. A LBE target was irradiated by 40MeV α-particles delivered from a cyclotron facility, India. Quantitative analysis of the irradiated target indicated the production of 210,209At, 207Po radionuclides in the target matrix. The 210,209At radionuclides were separated by precipitation of bulk Pb, Bi and NCA radiotoxic Po radionuclides.

Incorporation of no-carrier added 200,203Pb and 200,201,202Tl in calcium alginate and hesperidin incorporated calcium alginate beads.

When radioisotopes are injected to human body, instantly free radicals are generated due to the interaction of ionizing radiation with water and fluids present in the body. The vehicle carrying radionuclides into human body should therefore be designed in a way which could also eliminate or reduce such possibilities. For the first time we have used free radical scavenger hesperidin, a polyphenolic compound having a benzo-γ-pyrone with a benzene ring moiety for extraction of no-carrier added (NCA) 200,203Pb and 200,201,202Tl. We have modified CA beads by incorporation of a polyphenol (hesperidin) (CA-Hes). This tailor made beads were characterized and tested for their efficacy towards extraction of no-carrier-added lead and thallium radioisotopes from 40MeV α particle irradiated Hg2Cl2 target.

Separation of no-carrier-added rhenium from bulk tantalum by the sodium malonate-PEG aqueous biphasic system.

The aqueous biphasic system (ABS) involving sodium malonate-polyethylene glycol (PEG) phases has been applied for the first time for separation of no-carrier-added (183)Re (T1/2=70 d) from α-particle irradiated bulk tantalum target. The various ABS conditions were applied for investigating the separation by varying pH, temperature, PEG-molecular weight, concentration of salt. The extraction pattern was hardly affected by change in pH and the molecular weight of PEG. One step separation of nca (183)Re from Ta was achieved at the optimal conditions of (i) 50% (w/w) PEG-4000-2 M sodium malonate, 40 °C and (ii) 50% (w/w) PEG-4000-3 M sodium malonate, room temperature (27 °C).