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中和粒子对用于估算胸外沉积分数的聚氨酯泡沫采样效率的影响。

The effects of neutralized particles on the sampling efficiency of polyurethane foam used to estimate the extrathoracic deposition fraction.

作者信息

Tomyn Ronald L, Sleeth Darrah K, Thiese Matthew S, Larson Rodney R

机构信息

a Rocky Mountain Center for Occupational & Environmental Health , Department of Family & Preventive Medicine, University of Utah , Salt Lake City , Utah.

出版信息

J Occup Environ Hyg. 2016;13(2):133-40. doi: 10.1080/15459624.2015.1091958.

Abstract

In addition to chemical composition, the site of deposition of inhaled particles is important for determining the potential health effects from an exposure. As a result, the International Organization for Standardization adopted a particle deposition sampling convention. This includes extrathoracic particle deposition sampling conventions for the anterior nasal passages (ET1) and the posterior nasal and oral passages (ET2). This study assessed how well a polyurethane foam insert placed in an Institute of Occupational Medicine (IOM) sampler can match an extrathoracic deposition sampling convention, while accounting for possible static buildup in the test particles. In this way, the study aimed to assess whether neutralized particles affected the performance of this sampler for estimating extrathoracic particle deposition. A total of three different particle sizes (4.9, 9.5, and 12.8 µm) were used. For each trial, one particle size was introduced into a low-speed wind tunnel with a wind speed set a 0.2 m/s (∼40 ft/min). This wind speed was chosen to closely match the conditions of most indoor working environments. Each particle size was tested twice either neutralized, using a high voltage neutralizer, or left in its normal (non neutralized) state as standard particles. IOM samplers were fitted with a polyurethane foam insert and placed on a rotating mannequin inside the wind tunnel. Foam sampling efficiencies were calculated for all trials to compare against the normalized ET1 sampling deposition convention. The foam sampling efficiencies matched well to the ET1 deposition convention for the larger particle sizes, but had a general trend of underestimating for all three particle sizes. The results of a Wilcoxon Rank Sum Test also showed that only at 4.9 µm was there a statistically significant difference (p-value = 0.03) between the foam sampling efficiency using the standard particles and the neutralized particles. This is interpreted to mean that static buildup may be occurring and neutralizing the particles that are 4.9 µm diameter in size did affect the performance of the foam sampler when estimating extrathoracic particle deposition.

摘要

除化学成分外,吸入颗粒物的沉积部位对于确定暴露可能产生的健康影响也很重要。因此,国际标准化组织采用了一种颗粒物沉积采样规范。这包括前鼻孔(ET1)和后鼻及口腔通道(ET2)的胸外颗粒物沉积采样规范。本研究评估了放置在职业医学研究所(IOM)采样器中的聚氨酯泡沫插入物与胸外沉积采样规范的匹配程度,同时考虑了测试颗粒中可能出现的静电积聚。通过这种方式,该研究旨在评估中和后的颗粒是否会影响该采样器估算胸外颗粒物沉积的性能。总共使用了三种不同粒径(4.9、9.5和12.8 µm)的颗粒。对于每次试验,将一种粒径的颗粒引入风速设定为0.2 m/s(约40 ft/min)的低速风洞中。选择该风速是为了与大多数室内工作环境的条件紧密匹配。每种粒径的颗粒均进行两次测试,一次使用高压中和器将其中和,另一次作为标准颗粒保持其正常(未中和)状态。IOM采样器安装有聚氨酯泡沫插入物,并放置在风洞内的旋转人体模型上。计算所有试验的泡沫采样效率,以与标准化的ET1采样沉积规范进行比较。对于较大粒径的颗粒,泡沫采样效率与ET1沉积规范匹配良好,但对于所有三种粒径的颗粒,总体趋势是低估。威尔科克森秩和检验的结果还表明,仅在粒径为4.9 µm时,使用标准颗粒和中和颗粒的泡沫采样效率之间存在统计学上的显著差异(p值 = 0.03)。这被解释为意味着可能正在发生静电积聚,并且中和直径为4.9 µm的颗粒确实会影响泡沫采样器在估算胸外颗粒物沉积时的性能。

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