The Science of Adhesive Bonding and its Transfer to Technology

Author's Note

This article is based, in part, on a lecture given by the author on the occasion of his receipt of The Adhesion Society Award for Excellence in Adhesion Science, Sponsored by 3M at the Society's 14th Annual Meeting in Clearwater, Florida, U.S.A., February 1991. The author takes this opportunity to thank the Adhesion Society for the award and the 3M Corporation for its sponsorship. It is an honor to receive such a tribute from a society and a corporation that have done so much to advance the science and technology of adhesive bonding.     

Probability distributions of gas hydrate formation

Induction time distributions for gas hydrate formation were measured for gas mixtures of methane + propane at pressures up to 11.3 MPa using a high‐pressure automated lag time apparatus (HP‐ALTA). Measurements were made at subcooling temperatures between 4.3 and 13.5 K and, while isothermal induction times between 0 and 15,000 s were observed, the median isothermal induction times for the distributions ranged from 100 to 4000 s. A hyperbolic relationship between median induction time and subcooling was used to correlate the data. A graphical interpretation is presented that relates the two types of data that can be acquired by using the HP‐ALTA in one of two modes to study hydrate formation: induction time distributions at constant subcooling and formation temperature distributions observed during linear cooling ramps. The equivalence of these two modes provides a robust method for studying the variation of formation phenomena in different hydrate systems. © 2013 American Institute of Chemical Engineers AIChE J, 59: 2640–2646, 2013     

Challenges in nucleic acid‐lipid films for transfection

The use of surface‐based methods for the delivery of therapeutics has recently generated increasing interest. These platforms have tremendous potential to minimize detrimental side effects associated with systemic delivery by localizing the therapeutic vehicle, and thus provide higher local doses for improved efficacy. Cationic lipids are one of the most commonly used synthetic carriers for the delivery of genetic cargo, such as DNA and RNA. However, reports on the use of lipid‐based films for gene delivery are scarce. Here we investigate the use of a lipid‐based film for the in vitro delivery of plasmid DNA. Solid DNA‐lipid films show very low levels of transfection, while identical complexes prepared for bolus delivery provide high levels of transfection when used directly. We investigate the mechanism, whereby the activity of these solid‐state films is lost and suggest methods for circumventing these challenges and restoring the efficacy of these films as gene delivery platforms. © 2013 American Institute of Chemical Engineers AIChE J, 59: 3203–3213, 2013     

Fundamental thermo‐mechanical property modeling of triglyceride‐based thermosetting resins

The glass transition temperature (T_g) of acrylated triglycerides was clearly a function of the level of acrylation of triglyceride‐based polymers and was modeled using simple empirical relationships. We began by calculating the distribution of unsaturation sites in plant oils. We assumed a binomial distribution of chemical functionality that was added to these unsaturation sites to calculate the distribution of epoxides, acrylates, and reacted acrylates to predict the crosslink density, thermal softening, and dynamic mechanical behavior. The glass transition temperatures of n‐acrylated triglycerides were used as the relaxation temperatures of acrylated oils with a broad distribution of functionality for prediction of the modulus as a function of temperature. Essentially, the percent drop in the elastic modulus is equal to the percentage of n‐acrylated triglycerides in the acrylated oil with T_g less than that of the ambient temperature. The tan (δ) was also accurately predicted based on the percentage change of n‐functional triglycerides as the temperature changes from one relaxation temperature to the next. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Morphological and Elemental Classification of Freshly Emitted Soot Particles and Atmospheric Ultrafine Particles using the TEM/EDS

The Transmission Electron Microscopy (TEM) and Energy Dispersive Spectroscopy (EDS) were used to determine morphology and elemental composition of a variety of freshly emitted soot particles (acetylene flame, candle flame, kerosene flame, diesel exhaust, electric arc, plastic burning, styrofoam burning, wood burning [white oak and pine bark], and rice straw burning), which can be possible candidate soot in the ambient atmosphere, and ultrafine particles sampled in urban, industrial, and coastal sites during ultrafine particle formation events (combustion and photochemical events). By using mobility-classified non-refractory ((NH ₄ ) ₂ SO ₄ ) and refractory (Polystyrene latex (PSL) and salt (NaCl)) particles, limitation of the TEM was tested. Data showed that the TEM method can be used to examine shapes of both volatile particles such as (NH ₄ ) ₂ SO ₄ (100 nm) at low, but not high magnification (refer to low and high beam intensity, respectively), and non-volatile particles like NaCl (100 nm) and PSL (84 nm) at either low or high magnification. Distinct differences in morphological properties such as primary particle diameter, fractal dimension, and microstructure were observed among the different types of fresh soot particles. The atmospheric ultrafine particles were classified as agglomerates, sulfate mixtures (spherical), metallic oxides (spherical and polygonal), C-rich refractory (not agglomerated), C-rich non-refractory (not agglomerated), Si-rich (spherical), Na-rich (porous), or P-containing (non-spherical) particles. At the urban Gwangju site, a higher fraction of fresh and aged agglomerates was observed than at other sites. The C-rich non-refractory and sulfate mixtures were often observed in the photochemical event. The C-rich refractory particles were abundant at the Gwangju and Yeosu sites. The coastal Taean site had few agglomerates due to limited anthropogenic combustion source.     

Spatial Measurements of Ultrafine Particles Using an Engine Exhaust Particle SizerTM within a Local Community Downwind of a Major International Trade Bridge in Buffalo,New York

Ultrafine particles (UFP) can be defined as having at least one dimension that is less than 100 nanometers. Because of their dimensions, they exhibit unique properties that affect atmospheric transport, exposures, and possibly health endpoints. Freshly generated Diesel particulate matter (DPM) is predominantly in the ultrafine particle size range size range, which in practice is defined by the detection characteristics of the sampling instrument. During two seasons, an Engine Exhaust Particle Sizer^TM (TSI, St. Paul, MN) detects particles over a range of 5.6–560 nm was used to continuously measure real-time particle size distributions along several streets that extend from the Peace Bridge (PB), a major international trade bridge, into a the nearby adjacent neighborhood that has reported a high prevalence rate of asthma (Lwebuga-Mukasa 2000). The Peace Bridge connects Buffalo, NY, USA to Fort Erie, ON, Canada. During summer 2004, one minute average particle number concentrations were continuously monitored along neighborhood streets near the Peace Bridge Complex (PBC) plaza out to about 2 km. Ultrafine particle counts as a function of bridge traffic showed downwind UFP levels at 300 m ranging from 60,000–70,000 p/cm³. Upwind background UFP levels at the shore line of Lake Erie were typically 8,000–10,000 p/cm³ under similar traffic and meteorological conditions. During winter 2006, additional measurements were conducted in front of several homes that were part of a separate indoor-outdoor exposure study (McAuley et al. 2010 McAuley, T. R., Fisher, R., Zhou, X., Jaques, P. A. and Ferro, A. R. 2010. Relationships of Outdoor and Indoor Ultrafine Particles at Residences Downwind of a Major International Border Crossing in Buffalo, NY.. Indoor Air, 20: 298–308. [Crossref] , [Google Scholar]). Sampling at the homes was done during the weekdays when heavy diesel truck traffic was highest. Results showed that most of the UFP number concentrations fell between 10–20 nm in front of homes with UFP levels ranging from 59,000 p/cm³ at couple hundred m downwind to 81,000 p/cm³ several hundred m directly downwind of the Peace Bridge under similar diesel trucks traffic and meteorological conditions.     

Diffusion-Limited Versus Quasi-Equilibrium Aerosol Growth

Condensation of gas-phase material onto particulate matter is the predominant route by which atmospheric aerosols evolve. The traditional approach to representing formation of secondary organic aerosols (SOAs) is to assume instantaneous partitioning equilibrium of semivolatile organic compounds between gas and particle phases. Growth occurs as the vapor concentration of the species increases owing to gas-phase chemistry. The fundamental mathematical basis of such a condensation growth mechanism (quasi-equilibrium growth) has been lacking. Analytical solutions for the evolution of an organic aerosol size distribution undergoing quasi-equilibrium growth and irreversible diffusion-limited growth are obtained for open and closed systems. The quasi-equilibrium growth emerges as a limiting case for semivolatile species condensation when the rate of change of the ambient vapor concentration is slow compared with the rate of establishment of local gas-aerosol equilibrium. The results suggest that the growth mechanism in a particular situation might be inferred from the characteristics of the evolving size distribution. In certain conditions, a bimodal size distribution can occur during the condensation of a single species on an initially unimodal distribution.

Copyright 2012 American Association for Aerosol Research     

Enhancement of Surfactants in Nanoparticles Produced by an Electrospray Aerosol Generator

Electrospray aerosol generators (EAGs) disperse conducting solutions into air, promptly neutralize the particles to remove the excess charge, and evaporate the residual solvent with a dry air flow. For solutions containing multiple solutes, the particles may become enhanced in the more surface-active solutes. The extent of the enhancement was estimated for nanoparticles electrosprayed from a solution containing NaCl and surfactant sodium dodecyl sulfate (SDS) mixed in a 9:1 weight ratio. A tandem particle mobility analyzer was used to quantify the hygroscopic growth factor (GF). The relative fractions of NaCl and SDS in the particles were estimated from the measured GFs assuming that NaCl and SDS take up water independently of each other. The nanoparticles were considerably enhanced in SDS relative to the starting solution, with the NaCl:SDS weight ratio increasing with the distance from the EAG electrified capillary tip to the neutralizer, and reaching ～1:1 at the longest distances probed. The enhancement in SDS likely occurred during particle fission events as particles traveled from the capillary to the neutralizer. This study has practical ramifications for aerosol nanotechnology and aerosol-assisted drug delivery, which rely on EAG as an instrument of choice for nanoparticle generation.

Copyright 2012 American Association for Aerosol Research     

Effect of Dipping Temperature and Dipping Time on Drying Rate and Color Change of Grapes

Thompson seedless grapes (Vitis vinifera) were pretreated in potassium carbonate and ethyl oleate solutions for 1, 2, and 3 min at 30, 40, 50, and 60°C and dried in a convective air dryer at 60°C. The effect of dipping time and solution temperature on drying rate and color kinetics were investigated. Grapes dipped into the solution at 60°C for 2 and 3 min had the fastest drying rate. Among the seven semi theoretical models compared, the Midilli equation best described the drying curves of grapes for all dipping pretreatments. Color data were obtained using a machine vision system in CIE L*a*b* color space. Regardless of the dipping time and temperature applied, all raisins had varying degrees of brown coloring. At all dipping times and temperatures the highest R ² value was obtained for a* values, which followed zero-order reaction kinetics during drying.