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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 112 (1990), S. 4-7 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 42 (1994), S. 1402-1406 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Advanced materials research Vol. 29-30 (Nov. 2007), p. 287-290 
    ISSN: 1662-8985
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Confocal microscopy and water diffusivity measurements were used to characterise thedevelopment of defects in biofibre-reinforced composite materials. Biofibres swelled more than thematrix when the specimen was immersed in water, but the associated distortion of the matrix rarelycaused defects. The biofibres shrank faster than the matrix when the specimen was dried in air,causing debonding at the fibre-matrix interfaces and microcracks within the fibres. We started withcoarse technical fibres from the leaves of harakeke (Phormium tenax), treated a portion with 1%NaOH, and pulped a portion at 170 °C. Water diffusivities for the corresponding compositesincreased over the first 3 wet-dry cycles, particularly for the composite made with untreated fibre,but were too small to be of concern for the composite made from pulped fibre
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 34 (1995), S. 1196-1202 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The molecular mobility of the non-cellulosic polysaccharides in hydrated primary cell walls of three monocotyledons (Italian ryegrass, pineapple and onion) and one dicotyledon (cabbage) was studied using solid-state 13C NMR spectroscopy. These cell walls were chosen as they have different non-cellulosic polysaccharide compositions. By exploiting proton rotating-frame and spin-spin relaxation time constants three different cell wall domains which responded to cross-polarization experiments were identified. Most of the non-cellulosic polysaccharides occupied a mobile domain (C), but some occupied a partly rigid domain (B). Crystalline cellulose occupied a highly rigid domain (A). In the cell walls of Italian ryegrass and pineapple, domain C contained mainly glucuronoarabinoxylans and small amounts of rhamnogalacturonans; domain B contained small amounts of xyloglucans and galacturonans. However, in the cell walls of onion and cabbage, domain C contained mainly rhamnogalacturonans with galactans (in onion) or arabinans (in cabbage) as side chains; domain B contained galacturonans and xyloglucans. Single-pulse excitation was used on Italian ryegrass and cabbage cell walls to reveal signals from a highly mobile fourth domain (D). In Italian ryegrass cell walls domain D contained glucuronoarabinoxylans and small amounts of rhamnogalacturonan, whereas in cabbage cell walls it contained arabinan side chains of rhamnogalacturonans. A novel feature of the research was the use of solid-state 13C NMR spectroscopy to examine the molecular mobilities of the polysaccharides in monocotyledon cell walls that contain glucuronoarabinoxylans.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Munksgaard International Publishers
    Physiologia plantarum 116 (2002), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The primary walls of celery (Apium graveolens L.) parenchyma cells were isolated and their polysaccharide components characterized by glycosyl linkage analysis, cross-polarization magic-angle spinning solid-state 13C nuclear magnetic resonance (CP/MAS 13C NMR) and X-ray diffraction. Glycosyl linkage analysis showed that the cell walls consisted of mainly cellulose (43 mol%) and pectic polysaccharides (51 mol%), comprising rhamnogalacturonan (28 mol%), arabinan (12 mol%) and galactan (11 mol%). The amounts of xyloglucan (2 mol%) and xylan (2 mol%) detected in the cell walls were strikingly low. The small amount of xyloglucan present means that it cannot coat the cellulose microfibrils. Solid-state 13C NMR signals were consistent with the constituents identified by glycosyl linkage analysis and allowed the walls to be divided into three domains, based on the rigidity of the polymers. Cellulose (rigid) and rhamnogalacturonan (semi-mobile) polymers responded to the CP/MAS 13C NMR pulse sequence and were distinguished by differences in proton spin relaxation time constants. The arabinans, the most mobile polymers, responded to single-pulse excitation (SPE), but not CP/MAS 13C NMR. From solid-state 13C NMR of the cell walls the diameter of the crystalline cellulose microfibrils was determined to be approximately 3 nm while X-ray diffraction of the cell walls gave a value for the diameter of approximately 2 nm.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-882X
    Keywords: NMR spectroscopy ; alkali treatment ; dried/never-dried
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Carbon-13 NMR methods were used to monitor changes in the proportions of crystalline and non-crystalline cellulose, and the exposure of chains on crystallite surfaces, in samples of alkali-treated kraft pulp and regenerated cellulose. A large increase in the amount of disorderd cellulose, as a result of conversion to cellulose II, is the major effect of alkali treatment with kraft pulp. Removal of small crystallites is the major effect with regenerated cellulose. Samples were examined never-dried, or were vacuum-dried prior to remoistening for characterization. Changes in molecular ordering consistent with pore collapse and coalescence of crystallite surfaces accompanied the removal of water.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cellulose 4 (1997), S. 269-279 
    ISSN: 1572-882X
    Keywords: nuclear magnetic resonance ; cellulose Ialpha ; cellulose Ibeta ; fern
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Solid-state 13C NMR spectroscopy was used to characterize fibrous material cut from the midrib of a fern frond. Signals associated with cellulose crystallites were separated from those associated with the lignin--hemicellulosic matrix by exploiting differences in proton rotating-frame relaxation time constants. Heights of signals at 90.2 and 88.5 ppm, assigned to C-4 in cellulose Iα and Iβ, indicated similar proportions of the two crystalline forms. This observation conflicts with a suggestion that plant celluloses can be grouped into the two categories of Iα-rich and Iβ-rich.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1572-882X
    Keywords: nuclear magnetic resonance ; molecular disorder ; crystal surfaces
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Differences between values of proton rotating-frame spin relaxation time constants can be exploited to separate a solid-state13C NMR spectrum of cellulose into subspectra of crystalline and noncrystalline regions. Variations in chemical shifts and13C spin-lattice relaxation time constants can then be used to study variations in molecular order and disorder within each of the two broader categories. Mechanical damage during Wiley milling increases the content of noncrystalline cellulose and changes the nature of molecular disorder within that category. Resolution enhancement of the subspectrum assigned to crystalline cellulose reveals pairs of signals at 83.9 and 84.9 ppm (cellulose I) or 86.8 and 88.3 ppm (cellulose II) assigned to C-4 on well-ordered crystal surfaces. A broader peak in the subspectrum of crystalline cellulose I is assigned to poorly-ordered surfaces. Relative proportions in Avicel microcrystalline cellulose were estimated as: 54% in crystal interiors, 22% on well-ordered surfaces, 8% on poorly-ordered surfaces, 16% in domains of disorder extending more than a few nanometres.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-515X
    Keywords: carbon decomposition ; forest harvesting ; forest soil ; NMR spectroscopy ; phosphorus cycling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Phosphorus mineralization is chemically coupled with organic matter (OM) decomposition in surface horizons of a mixed-conifer forest soil from the Sierra Nevada, California, and is also affected by the disturbance caused by forest harvesting. Solution13C nuclear magnetic resonance (NMR) spectroscopy of NaOH extracts revealed a decrease of O-alkyl and alkyl-C fractions with increasing degree of decomposition and depth in the soil profile, while carbonyl and aromatic C increased. Solid-state13C-NMR analysis of whole soil samples showed similar trends, except that alkyl C increased with depth. Solution31P-NMR indicated that inorganic P (P1) increased with increasing depth, while organic-P (Po) fractions decreased. Close relationships between P mineralization and litter decomposition were suggested by correlations between P1 and C fractions (r = 0.82, 0.81, −0.87, and −0.76 for carbonyl, aromatic, alkyl and O-alkyl fractions, respectively). Correlations for diester-P and pyrophosphate with O-alkyl (r = 0.63 and 0.84) and inverse correlations with aromatics (r = −0.74 and −0.72) suggest that mineralization of these P fractions coincides with availability of C substrate. A correlation between monoester P and alkyl C (r = 0.63) suggests mineralization is linked to breakdown of structural components of the plant litter. NMR analyses, combined with Hedley-P fractionation, suggest that post-harvest buildup of labile P in decomposed litter increases the potential for leaching of P during the first post-harvest season, but also indicates reduced biological activity that transports P from litter to the mineral soil. Thus, P is temporarily stored in decomposed litter, preventing its fixation by mineral oxides. In the mineral horizons,31P-NMR provides evidence of decline in biologically-available P during the first post-harvest season.
    Type of Medium: Electronic Resource
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