Investigation of the dose rate dependency of the PAGAT gel dosimeter at low dose rates

Medical physicists need dosimeters such as gel dosimeters capable of determining three-dimensional dose distributions with high spatial resolution. To date, in combination with magnetic resonance imaging (MRI), polyacrylamide gel (PAG) polymers are the most promising gel dosimetry systems. The purpose of this work was to investigate the dose rate dependency of the PAGAT gel dosimeter at low dose rates. The gel dosimeter was used for measurement of the dose distribution around a Cs-137 source from a brachytherapy LDR source to have a range of dose rates from 0.97 Gy h^?1 to 0.06 Gy h^?1. After irradiation of the PAGAT gel, it was observed that the dose measured by gel dosimetry was almost the same at different distances (different dose rates) from the source, although the points nearer the source had been expected to receive greater doses. Therefore, it was suspected that the PAGAT gel is dose rate dependent at low dose rates. To test this further, three other sets of measurements were performed by placing vials containing gel at different distances from a Cs-137 source. In the first two measurements, several plastic vials were exposed to equal doses at different dose rates. An ionization chamber was used to measure the dose rate at each distance. In addition, three TLD chips were simultaneously irradiated in order to verify the dose to each vial. In the third measurement, to test the oxygen diffusion through plastic vials, the experiment was repeated again using plastic vials in a nitrogen box and glass vials. The study indicates that oxygen diffusion through plastic vials for dose rates lower than 2 Gy h^?1 would affect the gel dosimeter response and it is suggested that the plastic vials or (phantoms) in an oxygen free environment or glass vials should be used for the dosimetry of low dose rate sources using PAGAT gel to avoid oxygen diffusion through the vials.     

Verification of the 3D dose distribution in spinal radiosurgery by using a BANG3® polymer gel dosimeter

Journal of the Korean Physical Society - In intensity-modulated radiosurgery (IMRS) treatment, radiation delivery techniques require the ability to accurately verify complex three-dimensional (3D)...     

Enhancements in 3D dosimetry measurement using polymer gel and MRI

The effects of varying the concentrations of cross-linker N, $N^{\prime }$-methyelene-bis-acrylamide (BIS) from 2% to 4%, and 2-hydroxyethylacrylate (HEA) monomer from 2% to 4% at 5% gelatin on the dose response of BIS–HEA–gelatin (BHEAG) aqueous polymer gel dosimeters have been studied using magnetic resonance imaging (MRI) for relaxation rate ($R_2)$ of water proton. The dosimeters were irradiated with ⁶⁰Co teletherapy $\gamma$-ray source at a constant dose rate, receiving doses up to 30 Gy. The radiation polymerization occurs and increases with increasing initial dose. $R_2$ is found to decrease mono-exponentially with depth inside the polymer gel and depend strongly upon the initial concentrations of co-monomers (HEA and BIS). Dose–depth map for BHEAG gel was determined for different concentrations of co-monomer (HEA and BIS). The percentage dose depth was also evaluated which leads to a good agreement with the ionization chamber measurements.     

Fricke and polymer gel 2D dosimetry validation using Monte Carlo simulation

Complexity in modern radiotherapy treatments demands advanced dosimetry systems for quality control. These systems must have several characteristics, such as high spatial resolution, tissue equivalence, three-dimensional resolution, and dose-integrating capabilities. In this scenario, gel dosimetry has proved to be a very promising option for quality assurance. In this study, the feasibility of Fricke and polymer gel dosimeters suitably shaped in form of thin layers and optically analyzed by visible light transmission imaging has been investigated for quality assurance in external radiotherapy. Dosimeter irradiation was carried out with a 6-MV photon beam (CLINAC 600C). The analysis of the irradiated dosimeters was done using two-dimensional optical transmission images. These dosimeters were compared with a treatment plan system using Monte Carlo simulations as a reference by means of a gamma test with parameters of 1 mm and 2%. Results show very good agreement between the different dosimetric systems: in the worst-case scenario, 98% of the analyzed points meet the test quality requirements. Therefore, gel dosimetry may be considered as a potential tool for the validation of other dosimetric systems.     

变电压X射线多谱CT成像虚拟设计

复杂结构件在X射线成像时,由于射线透照方向上有效厚度差异大、成像器件动态范围受限等原因,单一电压下的射线图像易出现过曝光和欠曝光共存现象,投影信息缺失严重,无法进行CT重建,为此提出了变电压多谱CT成像理论与方法。通过改变电压改变X光谱分布,实现X光谱与检测对象有效厚度的匹配,扩展图像动态范围,确保检测对象投影信息的完整性;同时基于虚拟设计思想,建立了基于单能和多能的变电压虚拟CT模型,实现了变电压X射线CT成像的虚拟仿真。虚拟实验表明：变电压多谱CT成像原理是可行的,能够实现复杂结构件CT成像。     

Performance evaluation of PVdF gel polymer electrolytes

A series of gel polymer electrolytes containing PVdF as homo polymer, a mixture of 1:1 Ethylene Carbonate (EC) : Propylene Carbonate (PC) as plasticizer and lithium-bistrifluoromethane sulphone imide [imide — LiN (CF₃SO₂)₂] has been developed. Amounts of polymer (PVdF), plasticizer and the imide lithium salt have been varied as a function of their weight ratio composition in this regard. Dimensionally stable films possessing appreciable room temperature conductivity values have been obtained with respect to certain weight ratio compositions. However, conductivity data have been recorded at different possible temperatures, i.e., from 20 °C to 65 °C. XRD and DSC studies were carried out to characterize the polymer films for better amorphicity and reduced glass transition temperature, respectively. The electrochemical interface stability of the PVdF based gel polymer electrolytes over a range of storage period (24 h – 10 days) have been investigated using A.C. impedance studies. Test cells containing Li/gel polymer electrolyte (GPE)/Li have been subjected to undergo 50 charge-discharge cycles in order to understand the electrochemical performance behaviour of the dimensionally stable films of superior conductivity. The observed capacity fade of less than 20% even after 50 cycles is in favour of the electrochemical stability of the gel polymer electrolyte containing 27.5% PVdF −67.5 % EC+PC −5% imide salt. Cyclic voltammetry studies establish the possibility of a reversible intercalation — deintercalation process involving Li⁺ ions through the gel polymer electrolyte.     

The dependence of quartz OSL on stimulation energy

Quartz is the mineral most commonly used for sediment dating. In dating practice, the optically stimulated luminescence (OSL) of quartz is measured mainly using the stimulation light whose wavelength is 470 ± 30 nm. The parameters of traps active in the OSL process are also determined for this stimulation band. The zeroing of the OSL is the fundamental condition of applicability of the luminescence dating for specific sediment and takes place in sunlight whose spectrum differs significantly from the band 470 ± 30 nm. In order to be able to know the course of OSL process in nature, a wider knowledge of the dependency of the trap parameters on the stimulation band is needed. Here the results are presented for the OSL measurements carried out with different wavelengths of stimulation light. For each stimulation band the components of the OSL signal are determined by the fitting procedure, and in this way the wavelength dependence of an individual component is found. The experiment has been repeated for two temperatures of OSL detection – the room temperature, which corresponds to natural conditions, and for 125 °C, which is the temperature usually applied for OSL measurement in dating. Four OSL components are presented in both experimental series. The values of their optical cross-section changes along with stimulation energy and temperature, as it is predicted by the model of OSL process including crystal lattice vibrations.     

Electrochemical redox supercapacitors using PVdF-HFP based gel electrolytes and polypyrrole as conducting polymer electrode

Electrochemical redox supercapacitors have been fabricated using polymeric gel electrolytes polyvinylidene fluoride co-hexafluoropropylene (PVdF-HFP)–ethylene carbonate (EC)–propylene carbonate (PC)–MClO₄: M = Li, Na, (C₂H₅)₄N and electrochemically deposited polypyrrole as conducting polymer electrode. The performance of the capacitors have been characterized using a.c impedance spectroscopy, cyclic linear sweep voltammetry and galvanostatic charge–discharge techniques. The capacitors shows larger values of overall capacitance of about 14–25 mF cm^− 2 (equivalent to a single electrode specific capacitance of 78–137 F g^− 1 of polypyrrole), which corresponds to the energy density of 11–19 W h kg^− 1 and power density of 0.22–0.44 kW kg^− 1. The values of capacitance have been found to be almost stable up to 5000 cycles and even more. A comparison indicates that the capacitive behaviour and the capacitance values are not much affected with the size of cations of the salts incorporated in gel electrolytes, rather predominant role of anions is possible at the electrode–electrolyte interfaces. Furthermore the coulombic efficiencies of all the cells were found to be nearly 100% that is comparable to the liquid electrolytes based capacitors.     

Study of a novel porous gel polymer electrolyte based on TPU/PVdF by electrospinning technique

Investigation on a new electrospun gel polymer electrolyte consisting of thermoplastic polyurethane (TPU) and poly(vinylidene fluoride) (PVdF) has been made. Its characteristics were investigated by scanning electron microscopy, FT-IR, Differential Scanning Calorimeter (DSC) analysis. This kind of gel polymer electrolyte had a high ionic conductivity about 3.2 × 10^− 3 S cm^− 1 at room temperature, and exhibited a high electrochemical stability up to 5.0 V versus Li⁺/Li, good mechanical strength and stability to allow safe operation in rechargeable lithium-ion polymer batteries. A Li/GPE/LiFePO₄ cell delivered a high discharge capacity when it was evaluated at 0.1 °C—rate at 25 °C (167.8 mAh g^− 1). And a very stable cycle performance also existed under this low current density.     

基于加权TV正则化的X射线CT系统能谱估计方法

在CT硬化伪影校正、双能CT图像重建以及CT辐射剂量计算等实际应用中,X射线的能谱信息具有重要的作用。然而,由于透射测量方程组系数矩阵的病态性、X光子的统计涨落和噪声的干扰,使得EM等能谱估计方法难以获得较精细的能谱刻画。针对该问题,提出一种基于加权TV正则化的X射线CT系统能谱估计方法。首先采用能谱能量范围内带有不同K-edge的材料作为体模以降低投影测量方程之间的相关性。然后,利用CT成像系统的几何参数来获取投影测量数据所对应的准确透射长度信息来减小投影方程的测量误差。最后,综合利用透射衰减测量数据的保真性、轫致辐射能谱部分的连续性、特征辐射能谱部分的离散性、能谱的非负性和归一性以及平均有效衰减系数等信息,使用加权TV正则化方法建立目标函数,利用正则化理论中的L曲线准则通过黄金分割参数搜索策略求得最优正则化参数及对应的能谱估计结果。分别通过不同统计波动模型下的仿真能谱和实际测量数据对算法性能进行了验证,结果表明该方法与EM等方法相比,不受初始能谱的影响,有效提高了能谱估计结果的稳定性和准确性。     

Evidence of ion pair breaking by dispersed polymer in polymer gel electrolytes

Non-aqueous polymer gel electrolytes containing trifluoromethanesulfonic acid (HCF₃SO₃) and polyethylene oxide (PEO) as the gelling polymer has been studied. The increase in conductivity observed with the addition of PEO to liquid electrolytes has been explained to be due to the breaking of ion aggregates present in electrolytes at higher acid concentrations. The increase in free H⁺ ion concentration upon breaking of ion aggregates has also been observed in pH measurements and viscosity of gel electrolytes has been found to increase with PEO addition. Polymer gel electrolytes containing dimethylacetamide (DMA) have σ ∼ 10⁻² S/cm at room temperature and are stable over −50 to 125 °C range of temperature. Gels based on propylene carbonate (PC) and ethylene carbonate (EC) are stable in the −50 to 40 °C temperature range and loose their gelling nature above 40 °C.     

Evidence of ion pair breaking by dispersed polymer in polymer gel electrolytes

Non-aqueous polymer gel electrolytes containing trifluoromethanesulfonic acid (HCF₃SO₃) and polyethylene oxide (PEO) as the gelling polymer has been studied. The increase in conductivity observed with the addition of PEO to liquid electrolytes has been explained to be due to the breaking of ion aggregates present in electrolytes at higher acid concentrations. The increase in free H⁺ ion concentration upon breaking of ion aggregates has also been observed in pH measurements and viscosity of gel electrolytes has been found to increase with PEO addition. Polymer gel electrolytes containing dimethylacetamide (DMA) have σ ∼ 10⁻² S/cm at room temperature and are stable over −50 to 125 °C range of temperature. Gels based on propylene carbonate (PC) and ethylene carbonate (EC) are stable in the −50 to 40 °C temperature range and loose their gelling nature above 40 °C.     

基于局部线性关系的扇束X射线荧光CT几何校正研究

基于X射线管的X射线荧光计算机断层扫描术(CT)受多种因素影响,成像质量不佳,几何参数误差是制约其高质量图像重建的重要因素之一.本文分析成像二维平面模体与探测器相对位置偏移对投影数据的影响,并基于原始投影数据和原始重建图像再投影数据的局部线性关系实现几何偏移参数校正;利用Geant4模拟存在偏移参数的扇束X射线荧光CT系统,使用模拟投影数据验证校正方法.研究结果表明:该方法能计算出相对精确的几何偏移量,有效消除几何参数误差对重建图像的影响,校正后的重建图像信息熵降低,平均梯度和标准差提高,图像质量提升.     

Study of energy dependence of pion production by proton on copper target near 350 MeV

New measurement of the energy dependence of pion production on a copper target near 350-MeV proton energy has been performed. The E-170 experiment has been carried out at the Ring Cyclotron Facility of the Research Center for Nuclear Physics, Osaka University, Japan. A small enhancement of the low-energy pion production cross section was observed near the incident proton energy of 352 MeV. The text was submitted by the authors in English.     

Kinetics of water flow through a polymer gel

The water flow through the poly(acrylamide) gel under a constant water pressure is measured by newly designed apparatus. The Young modulus and Poisson’s ratio of the rod shape gels are measured by the uni-axial elongation experiments, which determine the longitudinal modulus independently from the water flow experiments. The time evolution of the water flow in the dilute gel is calculated based on the collective diffusion model of the polymer network coupled with the friction between the polymer network and the water. The calculated results are compared with the time evolution of the flow experiments, and the values of the longitudinal modulus and the friction coefficient are estimated. The estimated values are consistent with the results of our mechanical-response experiments and the light scattering experiments reported previously. We find that the time evolution of the water flow is well described by a single characteristic relaxation time predicted by our model for dilute gels.     

Laser energy dependence on femtosecond laser-induced nucleation of protein

We have investigated femtosecond laser-induced nucleation of hen egg-white lysozyme (HEWL) as a function of the laser pulse energy and pulse time width. This is the first recorded study to confirm that the femtosecond laser-induced nucleation of HEWL can be induced at a specific threshold laser energy. The threshold energy is comparable to that of cavitation bubble generation. The results strongly suggest that morphological changes in the solution are key factors for protein nucleation.     

Development and characterizations of PVdF-PEMA gel polymer electrolytes

A new class of gel polymer electrolytes comprising the blend of poly(ethyl methacrylate) (PEMA) and poly(vinylidene fluoride), the mixture of ethylene carbonate and propylene carbonate as a plasticizer, and lithium perchlorate (LiClO₄) as a salt was prepared using solvent casting technique. The formation of polymer–salt complexes has been confirmed by XRD analysis. Morphological and thermal studies have been performed using SEM and DMA analyses. A comparative look between PEMA and poly(methyl methacrylate) (PMMA) electrolytes has showed that PEMA electrolytes exhibited better electrochemical performances than PMMA electrolytes, despites its lower conductivity.     

Effect of polar aprotic solvents on hydroxyethyl cellulose-based gel polymer electrolyte

Quasi-solid bioelectrolytes based on hydroxyethyl cellulose (HEC) and sodium iodide (NaI) in three different polar aprotic solvent systems, dimethylformamide (DMF), dimethyl sulfoxide (DMSO), and dimethylacetamide (DMA), were fabricated and characterized. FTIR studies revealed active solvent-ion interactions in DMF-based electrolytes in comparison to DMA and DMSO. The effect of the solvent system on the crystallinity of HEC gel electrolytes was more significant at low NaI concentration. In each solvent system, the highest ionic conductivity was achieved at 70 wt% NaI and generally DMF-based electrolytes showed higher conductivity than the other solvents. The availability of multiple complexation sites present in DMF is ascribed to improvement in ion mobility and hence conductivity. Rheological analysis was carried out to elucidate the mechanical properties of the gels. Generally, the mechanical strength of the polymer gels was unaffected by the type of solvent.