18F− saturation yield in Large Volume cylindrical IBA target

Introduction In last decade increasing demand for clinical F-18 Fludeoxyglucose requires a greater F-18 fluoride production. From the other side increasing price of enriched O-18 water compel us to find the most effective way of F-18 activity production. One of the possible way, how to optimize and increase yield of F-18, is to increasing target current with retaining the same or less volume of enriched water. Optimization of F-18 production on IBA Large Volume cylindrical target is presented. Material and Methods Irradiations of [18O]H2O by 18MeV proton beams with intensities 40–55 μA were performed on CYCLON 18/9, IBA cyclotron and on LV cylindrical IBA target. Irradiated enriched water was transported to the hot cell using RDS (Radioactive Delivery System) system and was measured in Curriementor 4 Isotope Calibrator made by PTW. At the beginning it was necessary to satisfy several requirements: i) target and water cooling. Using a simple two dimensional equation we can roughly estimate the equilibrium temperature inside the target [1]: Δt = HT/Ak where: Δt = the temperature rise in the target chamber over cooling water temperature H = is the heat load T = thickness of metal wall A = area of metal in contact with target water k = thermal conductivity In our case with heat load 720 W (40 μA×18 MeV) is Δt = 78 oC. From the curve of boiling point of water as a function of pressure [2], we can observe t = 212 °C at 20 bar or 243 °C at 35 bar, respectively, which corresponds to max. heat load up to 90–95 µA of target current. ii) pressure and filling water volume. Filling water volume was from 2 to 2.15 ml to guarantee stop all beam in water. Also during experiments for safety reasons the operating pressure was limited to 35 bar as the window rupture pressure is > 50 bar for used 0.05 mm Havar foil. In this case increasing target volume with increasing current was provided with longer tube. Results and Conclusion The saturated yields of F-18 for 40 µA to 55 µA target currents are given in TABLE 1. No systematic decrease in yields with increasing target current was observed and yields were in line with the 230 ± 10 mCi/µA measured at acceptance test of target. The [18F]FDG yields from productions using the TRACERlab-Mx module are shown in FIGURE 1. All presented productions of F-18 were prepared with LV target with 55 µA. No decrease in the yield was observed with increasing beam current. It has been demonstrated that it is possible to produce routinely 250 GBq/2hr (6.8 Ci/2hr) of 18F-Fluoride using LV cylindrical target (operating conditions: 55 µA, 18 MeV, 98% enriched water). As the next step we want to test dual beam – 2×55 µA with two LV targets and expected activity about 500 GBq of 18F-Fluoride in 2 hours is expected

Preparation of routine automated synthesis of [11C]choline

Introduction [11C]choline is a very effective PET radiopharma-ceutical for the study of prostate cancer. To support the increasing demand for [11C]choline, several different synthetic approaches have been described in the literature, including different automated production methods using remote-controlled synthesis modules [1–4]. The most popular method uses a C18 Sep-Pak as solid support for methylation and, subsequently, a CM Sep-Pak for purification [2]. We report an optimized method for producing [11C]choline using only one CM Sep-Pak for both reaction and purification as was shown in the literature [4]. For synthesis of [11C]choline we used two modules Tracerlab FXC for preparation of methylation reagent [11C]CH3I and GPF-101 for [11C]choline synthesis. Material and Methods TracerlabFXC GE, GPF-101 Veenstra Instrument, 2-(dimethylamino)-ethanol (DMAE) ABX, Sep-Pak Light Accell Plus CM cation-exchange cartridges Waters used without conditioning, precursor 50 µL of DMAE dissolved in 25 µL of ethanol and loaded on a CM Sep-Pak. Schematic diagram of the automated system for the production of [11C]choline is given below. [11C]CH4 was produced in two standard Nitra target IBA irradiation of mixture 90 % N2/10 % H2 with 15 MeV protons using dual beam. Results and Conclusion [11C]CH4 was prepared in the targets and connected with Tracerlab FXC. [11C]CH3I was pre-pared in a loop in which allowed to react of elemental iodine at a temperature 720 oC. Con-version to [11C]CH3I usually is around 50% uncorrected activity. Activity is within the range 15–18 GBq of [11C]CH3I and time of production 10 min. Synthesis of [11C]choline is based on the reaction DMAE with [11C]CH3I on a Accell Plus CM cation-exchange column which serves both as a support for reaction and for separation of choline from DMAE by ethanol washing. The basic parameters are shown in TABLE 1. Beam current 2X 20 µA Irradiation time 30 min DMAE 50 µl Synthesis time from EOB 25 min Absolute yield without correction 6.6 GBq Radiochemical purity > 99 % Residual DMAE in product < 5 ppm Ethanol < 1000 mg/L pH 4.5–8.5 TABLE 1. Reaction parameters and result of production of [11C]choline syntheses Conclusion We have applied a simple synthesis method for [11C]choline preparation using automated commercial equipments with one column used both for reaction and separation purpose. The main advantage of using one column is lower contamination of the product [11C]choline with DMAE. When for synthesis of [11C]choline two columns C18 for synthesis and CM for separation is used, higher contamination of DMAE can be found in the product due to a release of DMAE from C18 column

Report of the Topical Group on Higgs Physics for Snowmass 2021: The Case for Precision Higgs Physics

A future Higgs Factory will provide improved precision on measurements of Higgs couplings beyond those obtained by the LHC, and will enable a broad range of investigations across the fields of fundamental physics, including the mechanism of electroweak symmetry breaking, the origin of the masses and mixing of fundamental particles, the predominance of matter over antimatter, and the nature of dark matter. Future colliders will measure Higgs couplings to a few per cent, giving a window to beyond the Standard Model (BSM) physics in the 1-10 TeV range. In addition, they will make precise measurements of the Higgs width, and characterize the Higgs self-coupling. This report details the work of the EF01 and EF02 working groups for the Snowmass 2021 study.Comment: 44 pages, 40 figures, Report of the Topical Group on Higgs Physics for Snowmass 2021. The first four authors are the Conveners, with Contributions from the other author

Separation techniques for quantification of radionuclides in environmental samples

The reliable and quantitative measurement of radionuclides is important in order to determine environmental quality and radiation safety, and to monitor regulatory compliance. We examined soil samples from Podunajske Biskupice, near the city of Pu, 241 Am) radionuclides. The area is adjacent to a refinery and hazardous waste processing center, as well as the municipal incinerator plant, and so might possess an unusually high level of ecotoxic metals. We found that the levels of both naturally occurring and anthropogenic radionuclides fell within the expected ranges, indicating that these facilities pose no radiological threat to the local environment. During the course of our analysis, we modified existing techniques in order to allow us to handle the unusually large and complex samples that were needed to determine the levels of Sr, which was less than we had expected. We also considered speed of separation and additional steps needed to prepare the sample for separation

Preparation of routine automated synthesis of [11C]choline

Introduction [11C]choline is a very effective PET radiopharma-ceutical for the study of prostate cancer. To support the increasing demand for [11C]choline, several different synthetic approaches have been described in the literature, including different automated production methods using remote-controlled synthesis modules [1–4]. The most popular method uses a C18 Sep-Pak as solid support for methylation and, subsequently, a CM Sep-Pak for purification [2]. We report an optimized method for producing [11C]choline using only one CM Sep-Pak for both reaction and purification as was shown in the literature [4]. For synthesis of [11C]choline we used two modules Tracerlab FXC for preparation of methylation reagent [11C]CH3I and GPF-101 for [11C]choline synthesis. Material and Methods TracerlabFXC GE, GPF-101 Veenstra Instrument, 2-(dimethylamino)-ethanol (DMAE) ABX, Sep-Pak Light Accell Plus CM cation-exchange cartridges Waters used without conditioning, precursor 50 µL of DMAE dissolved in 25 µL of ethanol and loaded on a CM Sep-Pak. Schematic diagram of the automated system for the production of [11C]choline is given below. [11C]CH4 was produced in two standard Nitra target IBA irradiation of mixture 90 % N2/10 % H2 with 15 MeV protons using dual beam. Results and Conclusion [11C]CH4 was prepared in the targets and connected with Tracerlab FXC. [11C]CH3I was pre-pared in a loop in which allowed to react of elemental iodine at a temperature 720 oC. Con-version to [11C]CH3I usually is around 50% uncorrected activity. Activity is within the range 15–18 GBq of [11C]CH3I and time of production 10 min. Synthesis of [11C]choline is based on the reaction DMAE with [11C]CH3I on a Accell Plus CM cation-exchange column which serves both as a support for reaction and for separation of choline from DMAE by ethanol washing. The basic parameters are shown in TABLE 1. Beam current 2X 20 µA Irradiation time 30 min DMAE 50 µl Synthesis time from EOB 25 min Absolute yield without correction 6.6 GBq Radiochemical purity > 99 % Residual DMAE in product < 5 ppm Ethanol < 1000 mg/L pH 4.5–8.5 TABLE 1. Reaction parameters and result of production of [11C]choline syntheses Conclusion We have applied a simple synthesis method for [11C]choline preparation using automated commercial equipments with one column used both for reaction and separation purpose. The main advantage of using one column is lower contamination of the product [11C]choline with DMAE. When for synthesis of [11C]choline two columns C18 for synthesis and CM for separation is used, higher contamination of DMAE can be found in the product due to a release of DMAE from C18 column

Problems in using high strength steels for welded structures

19.00; Translated from Czech (Zvaranie 1987 v. 36(7) p. 198-203)SIGLEAvailable from British Library Document Supply Centre- DSC:9023.19(VR--3375)T / BLDSC - British Library Document Supply CentreGBUnited Kingdo