Graphene sheets were produced through chemical exfoliation of natural graphite flake and hydrazine conversion. Subsequently, graphene sheets were assembled into a thin film, and microscale liquid droplets were placed onto the film surface for measurement of wettability and contact angle. It is found that a graphene oxide sheet is hydrophilic and a graphene sheet is hydrophobic. Isolated graphene layers seem more difficult to wet in comparison to graphite, and low adhesion work was found in the graphene-liquid interface. Approximation of solid-liquid interfacial energy with the equation of state theory was applied to determine the graphene surface energy. The results indicate that surface energy of graphene and graphene oxide is 46.7 and 62.1 mJ/m2, respectively, while natural graphite flake shows a surface free energy of 54.8 mJ/m2 at room temperature. These results will provide valuable guidance for the design and manufacturing of graphene-based biomaterials, medical instruments, structural composites, electronics, and renewable energy devices.

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It was the goal of the authors to create a set of reference cottons for maturity measurements. To achieve this they selected 104 cotton bales representing the two principal cultivated species. The vast majority of the bales originated in the USA, but some foreign-grown cotton bales were also selected (Egypt, Uzbekistan, Pakistan, Cameroon, Syria, Benin, and Australia). A representative sample of approximately 30 kg (70 pounds) was taken from each bale. Each sample was homogenized according to the protocol used by the International Cotton Calibration Standard Committee (ICCSC) to produce reference cottons. Eight sub-samples per bale were taken and a minimum of 500 cross-sections per sub-sample were analyzed. A broad range of average values of fiber perimeter and fiber maturity for the 104 bales were obtained. Evaluation of the mathematical and statistical relationships pertinent to maturity and fineness revealed that four critical criteria for adequate calibration standards were met. Therefore, this population of bales constitutes a good base for the calibration of the indirect measurement instruments for maturity and fineness.

Universal attenuated total reflectance Fourier transform infrared (UATR‐FTIR) spectroscopy and thermogravimetric analysis (TGA) were used to investigate the structural changes of cotton (Gossypium hirsutum L.) fibers as a function of developmental programming. The presence of noncellulosic compounds (wax, protein, hemicelluloses, pectic substances, amino acids, etc.) was evident from FTIR spectra of fibers at 10, 14, 17, and 20 dpa (day postanthesis). The vibration corresponding to the noncellulosic compounds disappeared at 36 dpa. Furthermore, independent TGA analysis supported the results obtained with FTIR, showing that the transition from primary cell wall synthesis to secondary cell wall synthesis occurs at or around 20 dpa. This study is the first to report on the use of the UATR‐FTIR and TGA to elucidate structural changes during cotton fiber development. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008

Cotton fiber maturity is a major yield component and an important fiber quality trait that is directly linked to the quantity of cellulose deposited during the secondary cell wall (SCW) biogenesis. Cotton fiber development consists of five major overlapping stages: differentiation, initiation, polar elongation, secondary cell wall development, and maturation. The transition period between 16 and 21 dpa (days post anthesis) is regarded to represent a major developmental stage between the primary cell wall and the SCW. Fourier Transform Infrared spectroscopy was used to investigate the structural changes that occur during the different developmental stages. The IR spectra of fibers harvested at different stages of development (10, 14, 17, 18, 19, 20, 21, 24, 27, 30, 36, 46, and 56 dpa) show the presence of vibrations located at 1,733 cm -1 (C=O stretching originating from esters or amides) and 1,534 cm -1 (NH 2 deformation corresponding to proteins or amino acids). The results converge towards the conclusion that the transition phase between the primary cell wall and the secondary cell wall occurs between 17 and 18 dpa in fibers from TX19 cultivar, while this transition occurs between 21 and 24 dpa in fibers from TX55 cultivar.

In this study, cotton fabric was successfully modified by titania nanosols prepared by means of the sol-gel process with tetrabutyl orthotitanate [Ti(OC(4)H(9))(4)] as the active ingredient. The cotton fabric was padded with the nanosol solution, dried at 60 degrees C, and cured at 150 degrees C. Scanning electron microscopy showed the presence of a titania film on the fiber surface. The photocatalytic properties of titania-nanosol-treated cotton fabric were investigated. The results showed that stains of coffee and red wine were successfully decomposed by exposure of the stained fabric to UV radiation. Furthermore, titania-nanosol treatment imparted to the cotton fabric a very good protection against UV radiation. The durability of the treatment was investigated by performing repeated home laundering, and the results showed no effect of laundering on the UV-protection efficiency.

Pollen grains and plant spores have emerged as a novel biomaterial for a broad range of applications including oral drug and vaccine delivery, catalyst support, and removal of heavy metals. However, before pollens can be used, their intrinsic biomolecules, which occupy a large part of the pollen inner cavity must be removed not only to create empty space but because they have potential to cause allergies when used in vivo. These intrinsic materials in the pollen core can be extracted through a chemical treatment to generate clean pollen shells. The commonly used method involves a series of sequential treatments with organic solvents, alkalis, and acids to remove the native pollen biomolecules. This method, though successful for treating lycopodium (Lycopodium clavatum) spores, fails for other species of pollens such as common ragweed (Ambrosia elatior) and thus prevents widespread investigation of different pollens. Herein, we report a new chemical treatment for obtaining clean pollen shells from multiple plant species. This new method involves sequential treatment with acetone, phosphoric acid, and potassium hydroxide. Scanning electron micrographs and protein quantification have shown that the new method can successfully produce clean, intact, and hollow shells from many pollen species including ragweed, sunflower, black alder, and lamb’s quarters. These results demonstrate the broad applicability of this method to clean pollens of different species, and paves the way to start investigating them for various applications.

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