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美国空军人员吸入喷气燃料暴露情况的特征分析

Characterization of inhalation exposure to jet fuel among U.S. Air Force personnel.

作者信息

Merchant-Borna Kian, Rodrigues Ema G, Smith Kristen W, Proctor Susan P, McClean Michael D

机构信息

Department of Environmental Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.

出版信息

Ann Occup Hyg. 2012 Jul;56(6):736-45. doi: 10.1093/annhyg/mes014. Epub 2012 Mar 20.


DOI:10.1093/annhyg/mes014
PMID:22433121
Abstract

BACKGROUND: Jet propulsion fuel-8 (JP-8) is the primary jet fuel used by the US military, collectively consuming ~2.5 billion gallons annually. Previous reports suggest that JP-8 is potentially toxic to the immune, respiratory, and nervous systems. The objectives of this study were to evaluate inhalation exposure to JP-8 constituents among active duty United States Air Force (USAF) personnel while performing job-related tasks, identify significant predictors of inhalation exposure to JP-8, and evaluate the extent to which surrogate exposure classifications were predictive of measured JP-8 exposures. METHODS: Seventy-three full-time USAF personnel from three different air force bases were monitored during four consecutive workdays where personal air samples were collected and analyzed for benzene, ethylbenzene, toluene, xylenes, total hydrocarbons (THC), and naphthalene. The participants were categorized a priori into high- and low-exposure groups, based on their exposure to JP-8 during their typical workday. Additional JP-8 exposure categories included job title groups and self-reported exposure to JP-8. Linear mixed-effects models were used to evaluate predictors of personal air concentrations. RESULTS: The concentrations of THC in air were significantly different between a priori exposure groups (2.6 mg m(-3) in high group versus 0.5 mg m(-3) in low, P < 0.0001), with similar differences observed for other analytes in air. Naphthalene was strongly correlated with THC (r = 0.82, P < 0.0001) and both were positively correlated with the relative humidity of the work environment. Exposures to THC and naphthalene varied significantly by job categories based on USAF specialty codes and were highest among personnel working in fuel distribution/maintenance, though self-reported exposure to JP-8 was an even stronger predictor of measured exposure in models that explained 72% (THC) and 67% (naphthalene) of between-worker variability. In fact, both self-report JP-8 exposure and a priori exposure groups explained more between-worker variability than job categories. CONCLUSIONS: Personal exposure to JP-8 varied by job and was positively associated with the relative humidity. However, self-reported exposure to JP-8 was an even stronger predictor of measured exposure than job title categories, suggesting that self-reported JP-8 exposure is a valid surrogate metric of exposure when personal air measurements are not available.

摘要

背景:喷气燃料8(JP - 8)是美国军方使用的主要喷气燃料,每年总消耗量约为25亿加仑。先前的报告表明,JP - 8可能对免疫、呼吸和神经系统有毒。本研究的目的是评估现役美国空军(USAF)人员在执行与工作相关任务时吸入JP - 8成分的情况,确定吸入JP - 8的显著预测因素,并评估替代暴露分类对测量的JP - 8暴露的预测程度。 方法:对来自三个不同空军基地的73名全职美国空军人员进行了连续四个工作日的监测,期间收集个人空气样本并分析其中的苯、乙苯、甲苯、二甲苯、总烃(THC)和萘。根据参与者在典型工作日接触JP - 8的情况,事先将他们分为高暴露组和低暴露组。其他JP - 8暴露类别包括职位组和自我报告的JP - 8暴露情况。使用线性混合效应模型评估个人空气浓度的预测因素。 结果:事先划分的暴露组之间空气中THC的浓度有显著差异(高暴露组为2.6 mg/m³,低暴露组为0.5 mg/m³,P < 0.0001),空气中其他分析物也观察到类似差异。萘与THC高度相关(r = 0.82,P < 0.0001),两者均与工作环境的相对湿度呈正相关。根据美国空军专业代码,THC和萘的暴露在不同工作类别中差异显著,在燃料分发/维护岗位工作的人员中暴露最高,不过在解释工人之间72%(THC)和67%(萘)变异性的模型中,自我报告的JP - 8暴露是测量暴露更强的预测因素。事实上,自我报告的JP - 8暴露和事先划分的暴露组比工作类别能解释更多的工人之间的变异性。 结论:个人对JP - 8的暴露因工作而异,且与相对湿度呈正相关。然而,自我报告的JP - 8暴露比职位类别是测量暴露更强的预测因素,这表明在无法进行个人空气测量时,自我报告的JP - 8暴露是暴露的有效替代指标。

相似文献

[1]
Characterization of inhalation exposure to jet fuel among U.S. Air Force personnel.

Ann Occup Hyg. 2012-7

[2]
Inhalation exposure to jet fuel (JP8) among U.S. Air Force personnel.

J Occup Environ Hyg. 2010-10

[3]
Urinary biomarkers of occupational jet fuel exposure among Air Force personnel.

J Expo Sci Environ Epidemiol. 2011-11-2

[4]
Personal exposure to JP-8 jet fuel vapors and exhaust at air force bases.

Environ Health Perspect. 2000-3

[5]
Benzene and naphthalene in air and breath as indicators of exposure to jet fuel.

Occup Environ Med. 2003-12

[6]
Dose-dependent production of urinary naphthols among workers exposed to jet fuel (JP-8).

Am J Ind Med. 2004-9

[7]
The Occupational JP8 Exposure Neuroepidemiology Study (OJENES): repeated workday exposure and central nervous system functioning among US Air Force personnel.

Neurotoxicology. 2011-7-28

[8]
Biological and health effects of exposure to kerosene-based jet fuels and performance additives.

J Toxicol Environ Health B Crit Rev. 2003

[9]
Dermal exposure to jet fuel (JP-8) in US Air Force personnel.

Ann Occup Hyg. 2005-10

[10]
Urinary polycyclic aromatic hydrocarbon (OH-PAH) metabolite concentrations and the effect of GST polymorphisms among US Air Force personnel exposed to jet fuel.

J Occup Environ Med. 2014-5

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[2]
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PLoS One. 2024

[3]
Potential Risks to Hearing Functions of Service Members From Exposure to Jet Fuels.

Am J Audiol. 2021-10-11

[4]
Occupational Exposures and Environmental Health Hazards of Military Personnel.

Int J Environ Res Public Health. 2021-5-18

[5]
Prevalence and trigger factors of functional gastrointestinal disorders among male civil pilots in China.

Sci Rep. 2021-1-21

[6]
Toxicokinetic Interaction between Hepatic Disposition and Pulmonary Bioactivation of Inhaled Naphthalene Studied Using -Null and CYP2A13/2F1-Humanized Mice with Deficient Hepatic Cytochrome P450 Activity.

Drug Metab Dispos. 2019-10-8

[7]
Bilateral Vestibular Dysfunction Associated With Chronic Exposure to Military Jet Propellant Type-Eight Jet Fuel.

Front Neurol. 2018-5-16

[8]
Volatile Organic Compounds in Blood as Biomarkers of Exposure to JP-8 Jet Fuel Among US Air Force Personnel.

J Occup Environ Med. 2016-1

[9]
Urinary polycyclic aromatic hydrocarbon (OH-PAH) metabolite concentrations and the effect of GST polymorphisms among US Air Force personnel exposed to jet fuel.

J Occup Environ Med. 2014-5

[10]
Jet fuel kerosene is not immunosuppressive in mice or rats following inhalation for 28 days.

J Toxicol Environ Health A. 2013

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