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Airplane dopes and doping

Description: Report details some examples of dopes and doping on airplanes and balloons and the various properties of different materials. Topics covered include cellulose nitrate dopes, cellulose acetate dopes, dope covers, application of dopes, and fireproof dopes
Date: 1919
Creator: Smith, W. H.
Partner: UNT Libraries Government Documents Department

In Vitro Determination of the Cellulose-Decomposing Rates of Twelve Denton County, Texas Soils

Description: In this study twelve types of top soil were collected under aseptic conditions. The cellulose-decomposing rates of these were compared in order to determine the relative rates in the cellulose-decomposing potential of the microorganisms involved. Furthermore, this investigation is designed to acquire pertinent information on the rate at which natural cellulose materials are returned to available plant food.
Date: 1950
Creator: Heather, Carl D.
Partner: UNT Libraries

Use of Sulphite Cellulose Extract as a Tanning Material

Description: Report issued by the Bureau of Standards over chemicals used for tanning leather hides. As stated in the introduction: "an investigation was conducted to determine the suitability of sulfite cellulose extracts, derived from the waste liquors discharged from paper pulp mills, for use in tanning hides for the manufacture of leather" (p. 309). This report includes tables, and photographs.
Date: November 1, 1926
Creator: Wallace, E. L. & Bowker, Roy Clement
Partner: UNT Libraries Government Documents Department

Feedstock and Web Analysis Using Mid-Infrared Diffuse Reflectance Spectroscopy and Imaging Spectroradiometry

Description: Potential applications of mid-infrared (MIR) spectroscopy in the forest products industry include on-line analysis of feedstock and web materials; these applications differ dramatically in purpose, speed, and overall chemical heterogeneity. Characterization of feedstock will enable sorting of the stock and/or wet chemistry adjustment prior to the web stage of paper production. Sorting will require imaging of the stock as well as classification of the wide variety of chemistry found in recycled stock. At the opposite end of the manufacturing process, on-line analysis of the web will enable adjustment of machine parameters to maximize product quality and minimize waste. Spectroscopic requirements for web analysis include high-speed capability and measurement precision. If successful, both applications could result in a reduction of resource waste, a reduction of plant pollution, and a reduction of energy use while simultaneously improving product quality. Here the progress towards feedstock and web analysis with MIR spectroscopy is presented. To date, work has progressed in three main areas: Diffuse Reflectance mid-Infrared Fourier Transform (DRIFT) spectroscopy of cellulose-based materials, chemometrics analysis, and research of MIR instrumentation for prototype development. The DRIFT spectroscopy data represents a database of the chemistries and spectroscopic signatures of interest to the applications discussed here. Over 50,000 spectra were obtained from cellulose-based materials infised with a wide variety of non-cellulose chemistry. Chemometrics analysis was performed on the DRIFT database to determine the quantitative and qualitative limits of the technique. Emphasis was placed on qualitative evaluation of spectroscopic signatures unique to the particular classes of cellulose-based material; thus, the degree to which classes could be sorted was determined. Finally, investigations of MIR instrumentation suitable for transfer of the technique from the lab-based instrument to a field ready prototype were made.
Date: September 15, 1997
Creator: Powell, G.L. & II, J.E. Parks
Partner: UNT Libraries Government Documents Department

The Dictyostelium discoideum cellulose synthase: Structure/function analysis and identification of interacting proteins

Description: OAK-B135 The major accomplishments of this project were: (1) the initial characterization of dcsA, the gene for the putative catalytic subunit of cellulose synthase in the cellular slime mold Dictyostelium discoideum; (2) the detection of a developmentally regulated event (unidentified, but perhaps a protein modification or association with a protein partner) that is required for cellulose synthase activity (i.e., the dcsA product is necessary, but not sufficient for cellulose synthesis); (3) the continued exploration of the developmental context of cellulose synthesis and DcsA; (4) the isolation of a GFP-DcsA-expressing strain (work in progress); and (5) the identification of Dictyostelium homologues for plant genes whose products play roles in cellulose biosynthesis. Although our progress was slow and many of our results negative, we did develop a number of promising avenues of investigation that can serve as the foundation for future projects.
Date: February 19, 2004
Creator: Blanton, Richard L.
Partner: UNT Libraries Government Documents Department

Cellulose and the Control of Growth Anisotropy

Description: The authors research aims to understand morphogenesis, focusing on growth anisotropy, a process that is crucial to make organs with specific and heritable shapes. For the award, the specific aims were to test hypotheses concerning how growth anisotropy is controlled by cell wall structure, particularly by the synthesis and alignment of cellulose microfibrils, the predominant mechanical element in the cell wall. This research has involved characterizing the basic physiology of anisotropic expansion, including measuring it at high resolution; and second, characterizing the relationship between growth anisotropy, and cellulose microfibrils. Important in this relationship and also to the control of anisotropic expansion are structures just inside the plasma membrane called cortical microtubules, and the research has also investigated their contribution to controlling anisotropy and microfibril alignment. In addition to primary experimental papers, I have also developed improved methods relating to these objectives as well as written relevant reviews. Major accomplishments in each area will now be described.
Date: April 1, 2004
Creator: Baskin, Tobias I.
Partner: UNT Libraries Government Documents Department

Production of bacterial cellulose from alternate feedstocks

Description: Production of bacterial cellulose by Acetobacter xylinum ATCC 10821 and 23770 in static cultures was tested from unamended food process effluents. Effluents included low- and high-solids potato effluents (LS and HS), cheese whey permeate (CW), and sugar beet raffinate (CSB). Strain 23770 produced 10% less cellulose from glucose than did 10821, and diverted more glucose to gluconate. Unamended HS, CW, and CSB were unsuitable for cellulose production by either strain, while LS was unsuitable for production by 10821. However, 23770 produced 17% more cellulose from LS than from glucose, indicating unamended LS could serve as a feedstock for bacterial cellulose.
Date: May 7, 2000
Creator: Thompson, D. N. & Hamilton, M. A.
Partner: UNT Libraries Government Documents Department

Temperature dependent rheology of surfactant-hydroxypropyl cellulose solutions.

Description: The rheology of 1-8% hydroxypropyl cellulose (HPC) solutions has been studied in the temperature range of 20-45 degrees Celsius. The results showed that the relative viscosity at each HPC concentration decreases with increasing temperature. The relative viscosity decreases drastically at about 43 degrees Celsius due to a phase transition. The influence of anionic surfactant, sodium dodecylsulfate (SDS), induced gelation of a 2% HPC solution. The HPC solutions gelled at surfactant SDS concentrations ranging from 0.4 to 1.0 critical micelle concentration (CMC). The gelation of the HPC/SDS hydrogel is explained in the surfactant SDD - bridged HPC linear polymer chains. The complex viscosity - concentration profile was determined below the CMC of the SDS - water pair. The peak itself was a function of frequency indicating the presence of two relaxation times within the gelled network.
Date: December 2002
Creator: Snively, C. Todd
Partner: UNT Libraries

The Effects of the Soil Conditioner, Superbio, Upon the Cellulose Decomposing Bacteria and the Crop Yield of a Soil

Description: The purpose of this investigation was to determine if a commercial soil conditioner, Superbio, can improve crop yield, and if the "advertised" soil improvement might be due to an increase in the activity and numbers of aerobic cellulose decomposing bacteria following treatment.
Date: August 1968
Creator: Gunn, Bruce Alan
Partner: UNT Libraries


Description: No Description Available.
Access: This item is restricted to UNT Community Members. Login required if off-campus.
Date: 1961
Creator: Hamilton, Richard
Partner: UNT College of Visual Arts + Design


Description: Micro-array experiments identified a number of Thermobifida fusca genes which were upregulated by growth on cellulose or plant biomass. Five of these genes were cloned, overexpressed in E. coli and the expressed proteins were purified and characterized. These were a xyloglucanase,a 1-3,beta glucanase, a family 18 hydrolase and twocellulose binding proteins that contained no catalytic domains. The catalyic domain of the family 74 endoxyloglucanase with a C-terminal, cellulose binding module was crystalized and its 3-dimensional structure was determined by X-ray crystallography.
Date: January 23, 2006
Creator: Wilson, David B.
Partner: UNT Libraries Government Documents Department

Supercomputer Provides Molecular Insight into Cellulose (Fact Sheet)

Description: Groundbreaking research at the National Renewable Energy Laboratory (NREL) has used supercomputing simulations to calculate the work that enzymes must do to deconstruct cellulose, which is a fundamental step in biomass conversion technologies for biofuels production. NREL used the new high-performance supercomputer Red Mesa to conduct several million central processing unit (CPU) hours of simulation.
Date: February 1, 2011
Partner: UNT Libraries Government Documents Department

Cellulose synthesizing Complexes in Vascular Plants andProcaryotes

Description: Continuing the work initiated under DE-FG03-94ER20145, the following major accomplishments were achieved under DE-FG02-03ER15396 from 2003-2007: (a) we purified the acsD gene product of the Acetobacter cellulose synthase operon as well as transferred the CesA cellulose gene from Gossypium into E. coli in an attempt to crystallize this protein for x-ray diffraction structural analysis; however, crystallization attempts proved unsuccessful; (b) the Acetobacter cellulose synthase operon was successfully incorporated into Synechococcus, a cyanobacterium2; (c) this operon in Synechococcus was functionally expressed; (d) we successfully immunolabeled Vigna cellulose and callose synthase components and mapped their distribution before and after wounding; (e) we developed a novel method to produce replicas of cellulose synthases in tobacco BY-2 cells, and we demonstrated the cytoplasmic domain of the rosette TC; (f) from the moss Physcomitrella, we isolated two full-length cDNA sequences of cellulose synthase (PpCesA1 and PpCesA2) and attempted to obtain full genomic DNA sequences; (g) we examined the detailed molecular structure of a new form of non-crystalline cellulose known as nematic ordered cellulose (=NOC)3.
Date: July 7, 2009
Creator: Brown, Richard M, Jr & Saxena, Inder Mohan
Partner: UNT Libraries Government Documents Department

Production of Bacterial Cellulose from Alternate Feedstocks

Description: Production of bacterial cellulose by Acetobacter xylinum ATCC 10821 and 23770 in static cultures was tested from unamended food process effluents. Effluents included low- and high-solids potato effluents (LS & HS), cheese whey permeate (CW), and sugar beet raffinate (CSB). Strain 23770 produced 10% less cellulose from glucose than did 10821, and diverted more glucose to gluconate. Unamended HS, CW, and CSB were unsuitable for cellulose production by either strain, while LS was unsuitable for production by 10821. However, 23770 produced 17% more cellulose from LS than from glucose, indicating unamended LS could serve as a feedstock for bacterial cellulose.
Date: May 1, 2000
Creator: Thompson, David Neil & Hamilton, Melinda Ann
Partner: UNT Libraries Government Documents Department

Extracellular oxidative metabolism of wood decay fungi

Description: Substantial progress has been made toward understanding the fundamental physiology and genetics of wood decay fungi, microbes that are capable of degrading all major components of plant cell walls. Efficient utilization of lignocellulosic biomass has been hampered in part by limitations in our understanding of enzymatic mechanisms of plant cell wall degradation. This is particularly true of woody substrates where accessibility and high lignin content substantially complicate enzymatic 'deconstruction'. The interdisciplinary research has illuminated enzymatic mechanisms essential for the conversion of lignocellulosics to simple carbohydrates and other small molecular weight products. Progress was in large part dependent on substantial collaborations with the Department of Energy's Joint Genome Institute (JGI) in Walnut Creek and Los Alamos, as well as the Catholic University, Santiago, Chile, the Royal Institute of Technology, Stockholm, the University of Minnesota, St. Paul, and colleagues at the University of Wisconsin and the Forest Products Laboratory. Early accomplishments focused on the development of experimental tools (2, 7, 22, 24-26, 32) and characterization of individual genes and enzymes (1, 3-5, 8, 9, 11, 14, 15, 17, 18, 23, 27, 33). In 2004, the genome of the most intensively studied lignin-degrading fungus, Phanerochaete chrysosporium, was published (21). This milestone lead to additional progress on this important model system (6, 10, 12, 13, 16, 28-31) and was further complemented by genome analysis of other important cellulose-degrading fungi (19, 20). These accomplishments have been highly cited and have paved the way for whole new research areas.
Date: April 21, 2010
Creator: Cullen, Daniel
Partner: UNT Libraries Government Documents Department

Cellulose Synthesis in Agrobacterium tumefaciens

Description: We have cloned the celC gene and its homologue from E. coli, yhjM, in an expression vector and expressed the both genes in E. coli; we have determined that the YhjM protein is able to complement in vitro cellulose synthesis by extracts of A. tumefaciens celC mutants, we have purified the YhjM protein product and are currently examining its enzymatic activity; we have examined whole cell extracts of CelC and various other cellulose mutants and wild type bacteria for the presence of cellulose oligomers and cellulose; we have examined the ability of extracts of wild type and cellulose mutants including CelC to incorporate UDP-14C-glucose into cellulose and into water-soluble, ethanol-insoluble oligosaccharides; we have made mutants which synthesize greater amounts of cellulose than the wild type; and we have examined the role of cellulose in the formation of biofilms by A. tumefaciens. In addition we have examined the ability of a putative cellulose synthase gene from the tunicate Ciona savignyi to complement an A. tumefaciens celA mutant. The greatest difference between our knowledge of bacterial cellulose synthesis when we started this project and current knowledge is that in 1999 when we wrote the original grant very few bacteria were known to synthesize cellulose and genes involved in this synthesis were sequenced only from Acetobacter species, A. tumefaciens and Rhizobium leguminosarum. Currently many bacteria are known to synthesize cellulose and genes that may be involved have been sequenced from more than 10 species of bacteria. This additional information has raised the possibility of attempting to use genes from one bacterium to complement mutants in another bacterium. This will enable us to examine the question of which genes are responsible for the three dimensional structure of cellulose (since this differs among bacterial species) and also to examine the interactions between the various proteins ...
Date: July 31, 2004
Creator: White, Alan R. & Matthysse, Ann G.
Partner: UNT Libraries Government Documents Department

Phase II Nuclide Partition Laboratory Study Influence of Cellulose Degradation Products on the Transport of Nuclides from SRS Shallow Land Burial Facilities

Description: Degradation products of cellulosic materials (e.g., paper and wood products) can significantly influence the subsurface transport of metals and radionuclides. Codisposal of radionuclides with cellulosic materials in the E-Area slit trenches at the Savannah River Site (SRS) is, therefore, expected to influence nuclide fate and transport in the subsurface. Due to the complexities of these systems and the scarcity of site-specific data, the effects of cellulose waste loading and its subsequent influence on nuclide transport are not well established.
Date: October 4, 1999
Creator: Serkiz, S.M.
Partner: UNT Libraries Government Documents Department

A pilot plant scale reactor/separator for ethanol from cellulosics. ERIP/DOE quarterly report no. 3 and 4

Description: The objective of this project is to develop and demonstrate a continuous, low energy process for the conversion of cellulosics to ethanol. This process involves a pretreatment step followed by enzymatic release of sugars and the consecutive simultaneous saccharification/fermentation (SSF) of cellulose (glucans) followed by hemi-cellulose (pentosans) in a multi-stage continuous stirred reactor separator (CSRS). During quarters 3 and 4, we have completed a literature survey on cellulase production, activated one strain of Trichoderma reesei. We continued developing our proprietary Steep Delignification (SD) process for biomass pretreatment. Some problems with fermentations were traces to bad cellulase enzyme. Using commercial cellulase enzymes from Solvay & Genecor, SSF experiments with wheat straw showed 41 g/L ethanol and free xylose of 20 g/L after completion of the fermentation. From corn stover, we noted 36 g/L ethanol production from the cellulose fraction of the biomass, and 4 g/L free xylose at the completion of the SSF. We also began some work with paper mill sludge as a cellulose source, and in some preliminary experiments obtained 23 g/L ethanol during SSF of the sludge. During year 2, a 130 L process scale unit will be operated to demonstrate the process using straw or cornstalks. Co-sponsors of this project include the Indiana Biomass Grants Program, Bio-Process Innovation.
Date: December 1, 1998
Creator: Dale, M.C.; Moelhman, M. & Butters, R.
Partner: UNT Libraries Government Documents Department