5 research outputs found
A full-scale tidal blade fatigue test using the FastBlade facility
Fatigue testing of tidal turbine blades requires the application of cyclic loads without the ability to match the natural frequency of the blade due to their high stiffness and the associated thermal issues of testing composite materials at those frequencies (i.e., 18–20 Hz). To solve this, loading the blades with an auxiliary system is necessary; in most cases, a conventional hydraulic system tends to be highly energy-demanding and inefficient. A regenerative digital displacement hydraulic pump system was employed in the FastBlade fatigue testing facility, which saved up to 75 % compared to a standard hydraulic system. A series of equivalent target loads were defined using Reynolds-Averaged Navier Stokes (RANS) simulations (based on on-site collected water velocity data) and utilised in FastBlade to demonstrate an efficient way to perform fatigue testing. During the test, a series of measurements were performed on the blade response and the Fastblade test structure itself, providing novel insights into the mechanical behaviour of a blade, and enabling improved testing practice for FastBlade. Without catastrophic failure, the blade withstood the principal tidal loading for 20 years (equivalent). This test data will enable FastBlade to identify improvements to the testing procedures, i.e., control strategies, load introduction, instrumentation layout, instrument calibration, and test design
A full-scale composite tidal blade fatigue test using single and multiple actuators
In order to perform fatigue testing on tidal turbine blades, it is necessary to apply cyclic loads that do not match the blade’s natural frequency. This is due to the high stiffness of the blades and the thermal challenges associated with testing composite materials at frequencies typically around 18–20 Hz. To overcome this challenge, auxiliary systems are used to load the blades. However, conventional hydraulic systems commonly used for this purpose are known to be energy-intensive and inefficient. In this work, we present results obtained at the FastBlade fatigue testing facility, which utilises a regenerative digital displacement hydraulic pump system to address these issues. This innovative system has proven to be highly efficient, resulting in up to 75% energy savings compared to standard hydraulic systems. To perform these tests, we first performed a series of Reynolds-Averaged Navier–Stokes (RANS) simulations using on-site water velocity data to determine equivalent target hydrodynamic loads. These target loads are applied to the blades using initially a single contact point and, later, three load contact points. The FastBlade facility showcases an effective approach to fatigue testing during these tests. Throughout the testing process, comprehensive measurements are taken to evaluate the response of the blades and the FastBlade test structure itself. These measurements provide valuable insights into the mechanical behaviour of the blades when a single or multi-actuator setup is used to match the root bending moment and contribute to the refinement of testing practices. Notably, the blades successfully endured the equivalent of 20 years of tides in an accelerated fatigue loading test without experiencing catastrophic failure. The data obtained from these tests will enable the identification of improvements in testing procedures, including control strategies, load introduction methods, instrumentation layout, instrument calibration, and test design. This knowledge will lead to enhanced performance and reliability of the FastBlade facility, further advancing the field of tidal turbine blade testing
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Estimated Effectiveness of JYNNEOS Vaccine in Preventing Mpox: A Multijurisdictional Case-Control Study — United States, August 19, 2022–March 31, 2023
As of March 31, 2023, more than 30,000 monkeypox (mpox) cases had been reported in the United States in an outbreak that has disproportionately affected gay, bisexual, and other men who have sex with men (MSM) and transgender persons (1). JYNNEOS vaccine (Modified Vaccinia Ankara vaccine, Bavarian Nordic) was approved by the Food and Drug Administration (FDA) in 2019 for the prevention of smallpox and mpox via subcutaneous injection as a 2-dose series (0.5 mL per dose, administered 4 weeks apart) (2). To expand vaccine access, an Emergency Use Authorization was issued by FDA on August 9, 2022, for dose-sparing intradermal injection of JYNNEOS as a 2-dose series (0.1 mL per dose, administered 4 weeks apart) (3). Vaccination was available to persons with known or presumed exposure to a person with mpox (postexposure prophylaxis [PEP]), as well as persons at increased risk for mpox or who might benefit from vaccination (preexposure mpox prophylaxis [PrEP]) (4). Because information on JYNNEOS vaccine effectiveness (VE) is limited, a matched case-control study was conducted in 12 U.S. jurisdictions,†including nine Emerging Infections Program sites and three Epidemiology and Laboratory Capacity sites,§ to evaluate VE against mpox among MSM and transgender adults aged 18-49 years. During August 19, 2022-March 31, 2023, a total of 309 case-patients were matched to 608 control patients. Adjusted VE was 75.2% (95% CI = 61.2% to 84.2%) for partial vaccination (1 dose) and 85.9% (95% CI = 73.8% to 92.4%) for full vaccination (2 doses). Adjusted VE for full vaccination by subcutaneous, intradermal, and heterologous routes of administration was 88.9% (95% CI = 56.0% to 97.2%), 80.3% (95% CI = 22.9% to 95.0%), and 86.9% (95% CI = 69.1% to 94.5%), respectively. Adjusted VE for full vaccination among immunocompromised participants was 70.2% (95% CI = -37.9% to 93.6%) and among immunocompetent participants was 87.8% (95% CI = 57.5% to 96.5%). JYNNEOS is effective at reducing the risk for mpox. Because duration of protection of 1 versus 2 doses remains unknown, persons at increased risk for mpox exposure should receive the 2-dose series as recommended by the Advisory Committee on Immunization Practices (ACIP),¶ regardless of administration route or immunocompromise status