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Occupational Exposure to Carbon Nanotubes and Nanofibers

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composite materials with local exhaust ventilationturned off. Four potential exposure-modifying fac<strong>to</strong>rswere assessed: (1) by composite type, (2) drillingrpm (low <strong>and</strong> high), (3) thickness of the composite,<strong>and</strong> (4) dry versus wet drilling. Replicate testmeasurements (10–30 measurements) lasting < 5minutes were performed on each composite material.A combination of real-time <strong>and</strong> integratedsamples were collected at the source <strong>and</strong> PBZ usingan FMPS, aerodynamic particle sizer (APS), CPC,diffusion charger, <strong>and</strong> cascade impac<strong>to</strong>r <strong>to</strong> measureaerosol particle size, concentration, <strong>and</strong> chemicalidentification. An electrostatic precipita<strong>to</strong>r (ESP)<strong>and</strong> thermal precipita<strong>to</strong>r (TP) were used <strong>to</strong> collectparticles directly on TEM grids for electron microscopyanalysis. Aerosol concentrations duringhigh rpm drilling generally were higher than forlow rpm drilling for all composite materials withaerosol concentrations found <strong>to</strong> be higher fromalumina composites. Wet drilling was observed <strong>to</strong>suppress the release of particles > 10 nm in diameter.High aspect-ratio fiber concentrations weredetermined using the sizing <strong>and</strong> counting criteriain NIOSH Method 7400 (> 5 µm long, aspect ratio> 3). Airborne exposure <strong>to</strong> both alumina fiber <strong>and</strong>CNT structures were found ranging in concentrationfrom 1.0 fibers/cm 3 (alumina composite) <strong>to</strong>1.9 fibers/cm 3 (carbon <strong>and</strong> CNT composite) forPBZ samples; similar concentrations were observedin area samples. Because sampling volume <strong>and</strong> fibersurface density on the samples were below theoptimal specification range of Method 7400, fiberconcentration values were determined <strong>to</strong> be firs<strong>to</strong>rder approximations. The authors concluded thathigher input energies (e.g., higher drilling rpms,larger drill bits) <strong>and</strong> longer drill times associatedwith thicker composites generally produced higherexposures, <strong>and</strong> that the drilling of CNT-based compositesgenerated a higher frequency of nanofibersthan had been previously observed during the cuttingof CNT-based composites [Bello et al. 2009].Cena <strong>and</strong> Peters [2011] evaluated the airbornerelease of CNT during the weighing of bulk CNT<strong>and</strong> the s<strong>and</strong>ing of epoxy nanocomposite sticksmeasuring 12.5 × 1.3 × 0.5 cm. Epoxy reinforcedtest samples were produced using MWCNT (Baytubes®)with 10–50 nm outer diameters <strong>and</strong> 1–20µm lengths. The purpose of the study was <strong>to</strong> (1)characterize airborne particles during h<strong>and</strong>ling ofbulk CNT <strong>and</strong> the mechanical processing of CNTcomposites, <strong>and</strong> (2) evaluate the effectiveness oflocal exhaust ventilation (LEV) hoods <strong>to</strong> captureairborne particles generated by s<strong>and</strong>ing CNT composites.Airborne particle number <strong>and</strong> respirablemass concentrations were measured using a CPC(particle diameters 0.01 <strong>to</strong> 1 µm) <strong>and</strong> OPC (particlediameters 0.3 <strong>to</strong> 20 µm). Respirable mass concentrationswere estimated using the OPC data.Samples for TEM analysis were also collected forparticle <strong>and</strong> CNT characterization. PBZ <strong>and</strong> sourceairborne concentrations were determined duringtwo processes: weighing bulk CNT <strong>and</strong> s<strong>and</strong>ingepoxy nanocomposite test sticks. <strong>Exposure</strong> measurementswere taken under three LEV conditions(no LEV, a cus<strong>to</strong>m fume hood, <strong>and</strong> a biologicalsafety cabinet). CPC <strong>and</strong> OPC particle concentrationswere measured inside a glove box in whichbulk CNT (600 mg) was transferred between two50-ml beakers; background particle concentrationswere measured inside the glove box beforethe process began. To study the s<strong>and</strong>ing process, aworker manually s<strong>and</strong>ed test sticks that contained2% by weight CNT. Aerosol concentrations weremeasured for 15–20 min in the worker’s breathingzone <strong>and</strong> at a site adjacent <strong>to</strong> the s<strong>and</strong>ing process.The s<strong>and</strong>ing process with no LEV was conductedon a 1.2 m by 2.2 m worktable. The s<strong>and</strong>ing wasalso conducted inside a cus<strong>to</strong>m fume hood thatconsisted of a simple vented enclosure that allowedairflow along all sides of the back panel but had nofront sash or rear baffles. The average face velocityof the fume hood was 76 ft/min. <strong>Exposure</strong>s fromthe s<strong>and</strong>ing process were also assessed while usinga biological safety cabinet (class II type A2).Particle number concentrations determined duringthe weighing process contributed little <strong>to</strong> tha<strong>to</strong>bserved in background samples (process <strong>to</strong> backgroundratio [P/B] = 1.06), however it did influencethe mass concentration (P/B = 1.79). TheGM respirable mass concentration inside the glove8 NIOSH CIB 65 • <strong>Carbon</strong> <strong>Nanotubes</strong> <strong>and</strong> <strong>Nanofibers</strong>

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