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Evaluation of Pump Pulsation in Respirable Size-Selective Sampling: Part III. Investigation of European Standard Methods

机译:可呼吸尺寸选择采样中泵脉动的评估:第三部分。欧洲标准方法调查

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摘要

Lee et al. (Evaluation of pump pulsation in respirable size-selective sampling: part I. Pulsation measurements. Ann Occup Hyg 2014a;58:60–73) introduced an approach to measure pump pulsation (PP) using a real-world sampling train, while the European Standards (EN) (EN 1232-1997 and EN 12919-1999) suggest measuring PP using a resistor in place of the sampler. The goal of this study is to characterize PP according to both EN methods and to determine the relationship of PP between the published method () and the EN methods. Additional test parameters were investigated to determine whether the test conditions suggested by the EN methods were appropriate for measuring pulsations. Experiments were conducted using a factorial combination of personal sampling pumps (six medium- and two high-volumetric flow rate pumps), back pressures (six medium- and seven high-flow rate pumps), resistors (two types), tubing lengths between a pump and resistor (60 and 90 cm), and different flow rates (2 and 2.5 l min−1 for the medium- and 4.4, 10, and 11.2 l min−1 for the high-flow rate pumps). The selection of sampling pumps and the ranges of back pressure were based on measurements obtained in the previous study (). Among six medium-flow rate pumps, only the Gilian5000 and the Apex IS conformed to the 10% criterion specified in EN 1232-1997. Although the AirChek XR5000 exceeded the 10% limit, the average PP (10.9%) was close to the criterion. One high-flow rate pump, the Legacy (PP = 8.1%), conformed to the 10% criterion in EN 12919-1999, while the Elite12 did not (PP = 18.3%). Conducting supplemental tests with additional test parameters beyond those used in the two subject EN standards did not strengthen the characterization of PPs. For the selected test conditions, a linear regression model [PPEN = 0.014 + 0.375 × PPNIOSH (adjusted R2 = 0.871)] was developed to determine the PP relationship between the published method () and the EN methods. The 25% PP criterion recommended by , average value derived from repetitive measurements, corresponds to 11% PPEN. The 10% pass/fail criterion in the EN Standards is not based on extensive laboratory evaluation and would unreasonably exclude at least one pump (i.e. AirChek XR5000 in this study) and, therefore, the more accurate criterion of average 11% from repetitive measurements should be substituted. This study suggests that users can measure PP using either a real-world sampling train or a resistor setup and obtain equivalent findings by applying the model herein derived. The findings of this study will be delivered to the consensus committees to be considered when those standards, including the EN 1232-1997, EN 12919-1999, and ISO 13137-2013, are revised.
机译:Lee等。 (可呼吸尺寸选择采样中泵浦脉动的评估:第一部分。脉动测量。AnnOccup Hyg 2014a; 58:60–73)介绍了一种使用真实采样火车测量泵浦脉动(PP)的方法,而欧洲人标准(EN)(EN 1232-1997和EN 12919-1999)建议使用电阻器代替采样器来测量PP。这项研究的目的是根据两种EN方法表征PP,并确定已发表的方法()和EN方法之间的PP关系。研究了其他测试参数,以确定EN方法建议的测试条件是否适合测量脉动。使用个人采样泵(六个中流量和两个高流量泵),背压(六个中流量和七个高流量泵),电阻器(两种类型),一个泵和电阻(60和90 cm),以及不同的流速(中等和4.4、10和11.2 l min -1 -1 >用于大流量泵)。采样泵的选择和背压的范围是基于先前研究()中获得的测量结果。在六个中流量泵中,只有Gilian5000和Apex IS符合EN 1232-1997中规定的10%标准。尽管AirChek XR5000超出了10%的限制,但平均PP(10.9%)仍接近标准。一款传统的高流量泵Legacy(PP = 8.1%)符合EN 12919-1999中10%的标准,而Elite12则不符合(PP = 18.3%)。使用超出两个EN标准的测试参数之外的其他测试参数进行补充测试不会增强PP的特性。对于选定的测试条件,开发了线性回归模型[PPEN = 0.014 + 0.375×PPNIOSH(调整后的R 2 = 0.871)],以确定已发布方法()和EN方法之间的PP关系。 。由重复测量得出的平均值所推荐的25%PP标准相当于11%PPEN。 EN标准中的10%通过/失败标准不是基于广泛的实验室评估,并且会不合理地排除至少一个泵(即本研究中的AirChek XR5000),因此,重复测量中更准确的平均11%标准应被取代。这项研究表明,用户可以使用实际采样序列或电阻器设置来测量PP,并通过应用本文推导的模型获得等效的发现。修订包括EN 1232-1997,EN 12919-1999和ISO 13137-2013在内的那些标准时,将把研究的结果提供给共识委员会。

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