Transitions from functionalization to fragmentation reactions of laboratory secondary organic aerosol (SOA) generated from the OH oxidation of alkane precursors

Functionalization (oxygen addition) and fragmentation (carbon loss) reactions governing secondary organic aerosol (SOA) formation from the OH oxidation of alkane precursors were studied in a flow reactor in the absence of NO(x). SOA precursors were n-decane (n-C10), n-pentadecane (n-C15), n-heptadecane (n-C17), tricyclo[5.2.1.0(2,6)]decane (JP-10), and vapors of diesel fuel and Southern Louisiana crude oil. Aerosol mass spectra were measured with a high-resolution time-of-flight aerosol mass spectrometer, from which normalized SOA yields, hydrogen-to-carbon (H/C) and oxygen-to-carbon (O/C) ratios, and C(x)H(y)+, C(x)H(y)O+, and C(x)H(y)O(2)+ ion abundances were extracted as a function of OH exposure. Normalized SOA yield curves exhibited an increase followed by a decrease as a function of OH exposure, with maximum yields at O/C ratios ranging from 0.29 to 0.74. The decrease in SOA yield correlates with an increase in oxygen content and decrease in carbon content, consistent with transitions from functionalization to fragmentation. For a subset of alkane precursors (n-C10, n-C15, and JP-10), maximum SOA yields were estimated to be 0.39, 0.69, and 1.1. In addition, maximum SOA yields correspond with a maximum in the C(x)H(y)O+ relative abundance. Measured correlations between OH exposure, O/C ratio, and H/C ratio may enable identification of alkane precursor contributions to ambient SOA.     

A Complete Detonator,Booster, and Main Charge Study of LX‐07/PBX 9502

A complete study of an exploding bridgewire detonator (EBW), an LX‐07 hemispherical booster and a PBX 9502 outer shell are described. Breakout times from all three are listed in terms of first impact on the booster, i.e., code times. Lucite windows are also used to obtain particle velocities at the edges of each explosive, and these are converted into explosive pressures. The key to modeling is the use of the profile of the aluminum detonator can as it impacts the booster, i.e., we need to know the curvature of the end of the booster can. Modeling even with coarse zoning shows that (i) using reactive flow in the booster is better than programmed burn, (ii) creating the flyer curvature helps, and (iii) creating the time differences of flyer impact helps even more.     

Infrared and Raman spectroscopy study of alkyl hydroxamic acid and alkyl hydroxamate isomers

The isomeric structures of alkyl hydroxamic acid, as well as its potassium salt, sodium salt, and an alcohol complex, have been characterized in the solid, liquid, and gaseous states by Fourier transform infrared (FT-IR) and FT-Raman spectroscopy. Raman spectroscopy provides insight into the long-standing debate over the isomeric composition of hydroxamates in the solid state and in an aqueous basic solution. IR and Raman results are not consistent with the enol isomer existing in the solid or liquid states of octyl or decyl hydroxamic acid, potassium hydroxamate, and sodium hydroxamate. The infrared and Raman spectra of these compounds provide clear and convincing evidence regarding their chemical structure, mainly from amide-type carbonyl, NH bending, and OH/NH stretching bands. Vibrational spectroscopy is sensitive to polar (FT-IR) and non-polar (FT-Raman) vibrations and the influence of ionic and hydrogen bonding on these vibrations, and these abilities are particularly useful for characterizing keto versus enol and trans versus cis conformations in alkyl hydroxamic acid and its salts. Evolved gas analysis (EGA) in a nitrogen gas environment of alkyl hydroxamic acid and its salts is also discussed. EGA data reveal that water is not incorporated into the solid-state crystal structure of alkyl hydroxamic acid or the potassium salt; however, the sodium salt form is found to have a stable hydrate conformer that is shown to affect the Z isomer (NH trans to carbonyl, OH cis to carbonyl) IR absorbance bands. EGA data also indicates results that could be of interest to bio-pharmaceutical applications involving nitric oxide donation.     

The Marginal Impact of a Publication on Citations,and Its Effect on Academic Pay

Scientometrics - There are good reasons for why academicians should care about citations to scholarly articles. An important one is that members of the academy operate essentially as independent...     

Regulation and Reconstruction of Cell Phenotype Gradients Along the Tendon-Bone Interface

Tendon–bone interface is prevalent in the human body. It is divided into four zones: tendon (soft tissue), unmineralized fibrocartilage, mineralized fibrocartilage, and bone (hard tissue). Tendon–bone interface is characterized by a cell phenotype gradient that appears in the different zones. The cell phenotype gradients at the tendon–bone interface are orchestrated by specific intracellular molecular mechanisms, extracellular factors, immune signals, and neurovascular factors. These features have inspired scientists to design systems that mimic natural cell phenotype gradients. These biomimetic systems include the construction of cell sheets, regulation of cellular microenvironments, and the design of gradient functional scaffolds. Exploration of methods to mimic cell phenotype gradients is instructional for future clinical applications in reconstituting the tendon–bone interface. The present review elucidates the gradient composition of the tendon–bone interface. The associated regulatory mechanisms and applications are discussed, with the anticipation of creating a mise en scène for future research in interface tissue engineering.     

Variable chemical process and radiative nonlinear impact on magnetohydrodynamics Cross nanofluid: An approach toward controlling global warming

Solar energy is the basic source of renewable energy, and it is being used for controlling global pollution/warming. As the Cross nanofluid is very useful for cooling solar devices, in this paper analysis of the global warming effect is investigated by incorporating the nonlinear thermal radiation over the exponentially extendable surface because it plays a major role related to solar energy absorption of nanofluid. Furthermore, the mathematical modeling of Cross nanofluid involving magnetic effect and diffusion is discussed by using the fact of chemical reaction. Chemical reaction finds astonishing applications in pollution studies, chemical processing equipment, and polymer production. As a result of this study, it is noticed that more magnetized conducting fluid controls the motion of fluids for both cases of shear thinning and shear thickening. Brownian motion parameter Nb affects the rate of the random motion of nanoparticles. Increased Nb temperature also increases due to these random movements of nanoparticles. That is the reason why pollutant nanoparticles spread in air as a result of global warming increase.