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Photosynthetic suspension cultures of higher plants offer an alternative approach to biomass production, potentially yielding
cellulosic material and protein on a continuous year-round basis. A bench-top hybrid photobioreactor was developed to study
photomixotrophic and photoautotrophic growth of Glycine max as a model system. Maximum biomass doubling times for photomixotrophic
and photoautotrophic growth were 1.87 and 3.92 d, respectively. The presence of exogenous sugars resulted in photomixotrophic
growth, reduced chlorophyll levels, and a reduction in photosynthetically-evolved oxygen. Depletion of carbohydrates from
the medium coincided with the beginning of stationary phase and an increase in oxygen evolution by the cells. A second growth
phase, prolonging cell viability, could be initiated by increasing the carbon dioxide from 2 to 5%, just before the onset
of stationary phase. Biomass from bioreactor cultured cells proved resistant to enzymatic attack without pretreatment. Composition
of the biomass was 7.8% lignin, 20.7% α-cellulose, 23% hemicellulose, 5.5% starch, 14.5% protein and 6.5% nucleic acids. 相似文献
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Edward T. Kopesky Stephen G. Boyes Neil Treat Robert E. Cohen Gareth H. McKinley 《Rheologica Acta》2006,45(6):971-981
Two distinct oligomeric species of similar mass and chemical functionality (M
w≈2,000 g/mol), one a linear methyl methacrylate oligomer (radius of gyration R
g≈1.1 nm) and the other a hybrid organic–inorganic polyhedral silsesquioxane nanocage (methacryl-POSS, r≈1.0 nm), were subjected to thermal and rheological tests to compare the behaviors of these geometrically dissimilar molecules over the entire composition range. The glass transition temperatures of the blends varied monotonically between the glass transition temperatures of the pure oligomer (T
g=−47.3°C) and the pure POSS (T
g=−61.0°C). Blends containing high POSS contents (with volume fraction φ
POSS≥0.90) exhibited enhanced enthalpy relaxation in differential scanning calorimetry (DSC) measurements, and the degree of enthalpy relaxation was used to calculate the kinetic fragility indices m of the oligomeric MMA (m=59) and the POSS (m=74). The temperature dependences of the viscosities were fitted by the free-volume based Williams–Landel–Ferry (WLF) and Vogel–Fulcher–Tammann (VFT) framework and a dynamic scaling relation. The calculated values of the fragility from the WLF–VFT fits were similar for the POSS (m=82) and for the oligomer (m=76), and the dynamic scaling exponent was similar for the oligomeric MMA and the POSS. Within the range of known fragilities for glass-forming liquids, the temperature dependence of the viscosity was found to be similarly fragile for the two species. The difference in shape of the nanocages and oligomer chains is unimportant in controlling the glass-forming properties of the blends at low volume fractions (φ
POSS<0.20). However, at higher volume fractions, adjacent POSS cages begin to crowd each other, leading to an increase in the fractional free volume at the glass transition temperature and the observed enhanced enthalpy relaxation in DSC. 相似文献
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David J. Lunn Sungbaek Seo Sang‐Ho Lee Raghida Bou Zerdan Kaila M. Mattson Nicolas J. Treat Alaina J. McGrath Will R. Gutekunst Jimmy Lawrence Allison Abdilla Athina Anastasaki Abigail S. Knight Bernhard V. K. J. Schmidt Morgan W. Bates Paul G. Clark Jonathan P. DeRocher Antony K. Van Dyk Craig J. Hawker 《Journal of polymer science. Part A, Polymer chemistry》2019,57(6):716-725
The synthesis and systematic comparison of a comprehensive library of well‐defined polymer architectures based on poly(acrylic acid) is reported. Through the development of new synthetic methodologies, linear, single branched, precision‐branched comb, and star polymers were prepared and their performance as dispersants was evaluated. The ability to accurately control chain lengths and branch points allows the subtle interplay between structure and dispersant performance to be defined and affords critical insights into the design of improved polymeric additives for coating formulations. The general industrial relevance of ionic polymers and branched macromolecular architectures supports these design rules for a wide range of other applications and materials, including as additives for personal care products and in water treatment. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 716–725 相似文献
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Solution processing of polymer semiconductor: Insulator blends—Tailored optical properties through liquid–liquid phase separation control 下载免费PDF全文
Christoph Hellmann Neil D. Treat Alberto D. Scaccabarozzi Joseph Razzell Hollis Franziska D. Fleischli James H. Bannock John de Mello Jasper J. Michels Ji‐Seon Kim Natalie Stingelin 《Journal of Polymer Science.Polymer Physics》2015,53(4):304-310
It has been demonstrated that the 0‐0 absorption transition of poly(3‐hexylthiophene) (P3HT) in blends with poly(ethylene oxide) (PEO) could be rationally tuned through the control of the liquid–liquid phase separation process during solution deposition. Pronounced J‐like aggregation behavior, characteristic for systems of a low exciton band width, was found for blends where the most pronounced liquid–liquid phase separation occurred in solution, leading to domains of P3HT and PEO of high phase purity. Since liquid–liquid phase separation could be readily manipulated either by the solution temperature, solute concentration, or deposition temperature, to name a few parameters, our findings promise the design from the out‐set of semiconductor:insulator architectures of pre‐defined properties by manipulation of the interaction parameter between the solutes as well as the respective solute:solvent system using classical polymer science principles. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 304–310 相似文献
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Christopher G. Shuttle Neil D. Treat Jian Fan Alessandro Varotto Craig J. Hawker Fred Wudl Michael L. Chabinyc 《Journal of Polymer Science.Polymer Physics》2012,50(3):174-179
The evaluation of the power conversion efficiency (PCE) of new materials for organic bulk heterojunction (BHJ) photovoltaics is difficult due to the large number of processing parameters possible. An efficient procedure to determine the optimum conditions for thermal treatment of polymer‐based bulk heterojunction photovoltaic devices using in situ current‐voltage measurements is presented. The performance of a new fullerene derivative, 1,9‐dihydro‐64,65‐dihexyloxy‐1,9‐(methano[1,2] benzomethano)fullerene[60], in BHJ photovolatics with poly(3‐hexylthiophene) (P3HT) was evaluated using this methodology. The device characteristics of BHJs obtained from the in situ method were found to be in good agreement with those from BHJs annealed using a conventional process. This fullerene has similar performance to 1‐(3‐methoxycarbonyl)propyl‐1‐phenyl‐[6,6]‐methano fullerene in BHJs with P3HT after thermal annealing. For devices with thickness of 70 nm, the short circuit current was 6.24 mA/cm2 with a fill factor of 0.53 and open circuit voltage of 0.65 V. The changes in the current‐voltage measurements during thermal annealing suggest that the ordering process in P3HT dominates the improvement in power conversion efficiency. © 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012 相似文献
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Simultaneous Preparation of Multiple Polymer Brushes under Ambient Conditions using Microliter Volumes 下载免费PDF全文
Benjaporn Narupai Dr. Zachariah A. Page Dr. Nicolas J. Treat Alaina J. McGrath Dr. Christian W. Pester Emre H. Discekici Neil D. Dolinski Dr. Gregory F. Meyers Prof. Javier Read de Alaniz Prof. Craig J. Hawker 《Angewandte Chemie (International ed. in English)》2018,57(41):13433-13438
The fabrication of well‐defined, multifunctional polymer brushes under ambient conditions is described. This facile method uses light‐mediated, metal‐free atom‐transfer radical polymerization (ATRP) to grow polymer brushes with only microliter volumes required. Key to the success of this strategy is the dual action of N‐phenylphenothiazine (PTH) as both an oxygen scavenger and polymerization catalyst. Use of simple glass cover slips results in a high degree of spatial and temporal control and allows for multiple polymer brushes to be grown simultaneously. The preparation of arbitrary 3D patterns and functional/emissive polymer brushes demonstrates the practicality and versatility of this novel strategy. 相似文献
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Ryan G. Ezell Irene Gorman Brad Lokitz Neil Treat Shawn D. Mcconaughy Charles L. Mccormick 《Journal of polymer science. Part A, Polymer chemistry》2006,44(15):4479-4493
Low‐charge‐density amphoteric copolymers and terpolymers composed of acrylamide, (3‐acrylamidopropyl)trimethyl ammonium chloride, and the amino acid derived monomers (e.g., N‐acryloyl valine, N‐acryloyl alanine, and N‐acryloyl aspartate) were prepared via free‐radical polymerization in aqueous media to yield terpolymers with random charge distributions and homogeneous compositions. Sodium formate (NaOOCH) was employed as a chain transfer agent during the polymerization to suppress gel effects and broadening of the molecular weight distribution. Terpolymer compositions were determined by 13C and 1H NMR spectroscopy. Terpolymer molecular weights and polydispersity indices were obtained via size exclusion chromatography/multi‐angle laser light scattering, and hydrodynamic diameter values were obtained via dynamic light scattering. The solution properties of low‐charge‐density amphoteric copolymers and terpolymers have been studied as a function of solution pH, ionic strength, and polymer concentration. The low‐charge‐density terpolymers display excellent solubility in deionized (DI) water with no phase separation. The charge‐balanced terpolymers exhibit antipolyelectrolyte behavior at pH values ≥(6.5 ± 0.2). As solution pH is decreased, these charge‐balanced terpolymers become increasingly cationic because of the protonation of the anionic repeat units. Charge‐imbalanced terpolymers generally demonstrate polyelectrolyte behavior, although the effects of intramolecular electrostatic interactions (e.g., polyampholyte effects) on the hydrodynamic volume are evident at certain values of solution pH and salt concentration. The aqueous solution behavior (i.e., globule‐to‐coil transition at the isoelectric point in the presence of salt and globule elongation with increasing charge asymmetry) of the terpolymers in the dilute regime correlates well with that predicted by the polyampholyte solution theories of Dobrynin and Rubinstein as well as Kantor and Kardar. Examination of comonomer charge density, hydrogen‐bonding ability, and spacer group (e.g., the moiety separating the ionic group from the polymer chain) indicates that conformational restrictions of the amino acid comonomers result in increased chain stiffness and higher solution viscosities in DI water and brine solutions. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4479–4493, 2006 相似文献
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Benjamin F. Hartmeier Michael A. Brady Neil D. Treat Maxwell J. Robb Thomas E. Mates Alexander Hexemer Cheng Wang Craig J. Hawker Edward J. Kramer Michael L. Chabinyc 《Journal of polymer science. Part A, Polymer chemistry》2016,54(2):237-246
Ternary organic blends have potential in realizing efficient bulk heterojunction (BHJ) organic solar cells by harvesting a larger portion of the solar spectrum than binary blends. Several challenging requirements, based on the electronic structure of the components of the ternary blend and their nanoscale morphology, need to be met in order to achieve high power conversion efficiency in ternary BHJs. The properties of a model ternary system comprising two donor polymers, poly(3-hexylthiophene) (P3HT) and a furan-containing, diketopyrrolopyrrole-thiophene low-bandgap polymer (PDPP2FT), with a fullerene acceptor, PC61BM, were examined. The relative miscibility of PC61BM with P3HT and PDPP2FT was examined using diffusion with dynamic secondary ion mass spectrometry (dynamic SIMS) measurements. Grazing incidence small and wide angle X-ray scattering analysis (GISAXS and GIWAXS) were used to study the morphology of the ternary blends. These measurements, along with optoelectronic characterization of ternary blend solar cells, indicate that the miscibility of the fullerene acceptor and donor polymers is a critical factor in the performance in a ternary cell. A guideline that the miscibility of the fullerene in the two polymers should be matched is proposed and further substantiated by examination of known well-performing ternary blends. The ternary blending of semiconducting components can improve the power conversion efficiency of bulk heterojunction organic photovoltaics. The blending of P3HT and PDPP2FT with PC61BM leads to good absorptive coverage of the incident solar spectrum and cascading transport energy levels. The performance of this ternary blend reveals the impact of the miscibility of PC61BM in each polymer as a function of composition, highlighting an important factor for optimization of ternary BHJs. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 237–246 相似文献
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