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  • Surface physics, nanoscale physics, low-dimensional systems  (4,242)
  • Physics  (2,680)
  • AERODYNAMICS
  • Adaptation
  • 2010-2014  (4,266)
  • 1980-1984  (4,774)
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  • 1
    Unknown
    Amsterdam ; New York : North-Holland Pub. Co
    Keywords: DDC 530.1 ; LC QC20 ; Mathematical physics ; Physics ; Quantum theory ; Relativity (Physics)
    ISBN: 9780444875853
    Language: English
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  • 2
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    Accademia di Scienze Fisiche e Matematiche di Napoli
    Publication Date: 2017-04-04
    Description: This paper aims to trace the documentary history of the Royal Collection of Physics Apparatus,currently housed in the Physics Museum at the Federico II University of Naples...
    Description: Published
    Description: 47 - 59
    Description: 3.10. Storia ed archeologia applicate alle Scienze della Terra
    Description: N/A or not JCR
    Description: reserved
    Keywords: History of Science ; Physics ; Scientific Collection ; Naples ; 05. General::05.03. Educational, History of Science, Public Issues::05.03.99. General or miscellaneous
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 3
    Publication Date: 2017-04-03
    Description: (extended abstract)
    Description: INGV, Regione Sicilia, Ministero Sviluppo Economico
    Description: Published
    Description: Ettore Majorana Foundation and Centre for Scientific Culture, Erice, Sicily
    Description: 5.9. Formazione e informazione
    Description: open
    Keywords: Inertia ; Physics ; Fluid Dynamics ; 05. General::05.03. Educational, History of Science, Public Issues::05.03.99. General or miscellaneous ; 05. General::05.05. Mathematical geophysics::05.05.99. General or miscellaneous ; 05. General::05.09. Miscellaneous::05.09.99. General or miscellaneous
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Extended abstract
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  • 4
    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2009. This is the author's version of the work. It is posted here by permission of Blackwell for personal use, not for redistribution. The definitive version was published in Ecology Letters 12 (2009): E15-E18, doi:10.1111/j.1461-0248.2009.01332.x.
    Description: Hartley et al. question whether reduction in Rmass, under experimental warming, arises because of the biomass method. We show the method they treat as independent yields the same result. We describe why the substrate-depletion hypothesis cannot alone explain observed responses, and urge caution in the interpretation of the seasonal data.
    Description: This research was supported by the Office of Science (BER), U.S. Department of Energy, the Andrew W. Mellon Foundation and U.S. National Science Foundation grants to the Coweeta LTER program.
    Keywords: Acclimation ; Adaptation ; Soil respiration ; Thermal biology ; Temperature ; Carbon cycling ; Climate change ; Climate warming ; Microbial community ; CO2
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 5
    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2012. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Journal of Ecology 100 (2012): 841-851, doi:10.1111/j.1365-2745.2012.01984.x.
    Description: Reciprocal transplant experiments designed to quantify genetic and environmental effects on phenotype are powerful tools for the study of local adaptation. For long-lived species, especially those in habitats with short growing seasons, however, the cumulative effects of many years in novel environments may be required for fitness differences and phenotypic changes to accrue. We returned to two separate reciprocal transplant experiments thirty years after their initial establishment in interior Alaska to ask whether patterns of differentiation observed in the years immediately following transplant have persisted. We also asked whether earlier hypotheses about the role of plasticity in buffering against the effects of selection on foreign genotypes were supported. We censused survival and flowering in three transplant gardens created along a snowbank gradient for a dwarf shrub (Dryas octopetala) and six gardens created along a latitudinal gradient for a tussock-forming sedge (Eriophorum vaginatum). For both species, we used an analysis of variance to detect fitness advantages for plants transplanted back into their home site relative to those transplanted into foreign sites. For D. octopetala, the original patterns of local adaptation observed in the decade following transplant appeared even stronger after three decades, with the complete elimination of foreign ecotypes in both fellfield and snowbed environments. For E. vaginatum, differential survival of populations was not evident 13 years after transplant, but was clearly evident 17 years later. There was no evidence that plasticity was associated with increased survival of foreign populations in novel sites for either D. octopetala or E. vaginatum. Synthesis. We conclude that local adaptation can be strong, but nevertheless remain undetected or underestimated in short-term experiments. Such genetically-based population differences limit the ability of plant populations to respond to a changing climate.
    Description: Funding for this research was provided by National Science Foundation grant ARC-0908936 with additional support from NSF-BSR-9024188.
    Keywords: Adaptation ; Dryas octopetala ; Ecological genetics and ecogenomics ; Eriophorum vaginatum ; Genetic differentiation ; Phenotypic plasticity ; Tussock tundra
    Repository Name: Woods Hole Open Access Server
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  • 6
    Publication Date: 2022-05-26
    Description: Author Posting. © The Author(s), 2009. This is the author's version of the work. It is posted here by permission of IOP Publishing for personal use, not for redistribution. The definitive version was published in Environmental Research Letters 4 (2009): 044008, doi:10.1088/1748-9326/4/4/044008.
    Description: Rising sea level threatens existing coastal wetlands. Overall ecosystems could often survive by migrating inland, if adjacent lands remained vacant. On the basis of 131 state and local land use plans, we estimate that almost 60% of the land below 1 m along the US Atlantic coast is expected to be developed and thus unavailable for the inland migration of wetlands. Less than 10% of the land below 1 m has been set aside for conservation. Environmental regulators routinely grant permits for shore protection structures (which block wetland migration) on the basis of a federal finding that these structures have no cumulative environmental impact. Our results suggest that shore protection does have a cumulative impact. If sea level rise is taken into account, wetland policies that previously seemed to comply with federal law probably violate the Clean Water Act.
    Keywords: Climate change ; Adaptation ; Land use planning ; Sea-level rise ; Wetland migration ; Shore protection
    Repository Name: Woods Hole Open Access Server
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  • 7
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    Calcified tissue international 36 (1984), S. S118 
    ISSN: 1432-0827
    Keywords: Bone ; Strain ; Remodeling ; Adaptation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary For bone to remodel adaptively, the cells responsible should follow some algorithm. Nine different loading situations and structures are discussed. It seems that either algorithm must be extremely complex, or cells in different structures must follow different algorithms.
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  • 8
    ISSN: 1432-1017
    Keywords: Receptor potential ; Intracellular and extracellular calcium concentration ; Intensity dependence ; Adaptation ; Sensitivity control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract The light-induced membrane voltage response (receptor potential, ReP) and the absorption change of the intracellularly injected calcium indicator arsenazo III (arsenazo response) were recorded simultaneously in Limulus ventral nerve photoreceptor cells. A double pulse technique was applied for stimulation. After pressure injection of the indicator into the cell absorption changes were measured at 646 nm to obtain a measure of the changes of the intracellular calcium ion concentration. 1. The size of the arsenazo response increases with increasing intensity of the light stimulus. The intensity dependence of the size of the arsenazo response δAmax shows almost no correlate with the peak amplitude of the ReP, but correlates rather well with the time integral of the ReP. 2. Decreasing light adaptation (caused by prolongation of the repetition time of the pulse pairs) leads to an increase in size of the arsenazo response. Also here δAmax correlates better with the time integral of the ReP than with its peak amplitude. 3. Lowering the calcium concentration in the superfusate (from 10 mmol/l to ca. 40 Μmol/l) causes after ca. 10 min a drastical diminution of the arsenazo response to values below the noise level, and a less marked reduction in size of the ReP. The falling phase of the ReP is slower. After return to normal calcium concentration the arsenazo response recovers partly in ca. 50 min, while the ReP recovers faster. The results show two opposite correlations between ReP and arsenazo response: Increase in size and duration of the ReP causes a greater transient increase of the intracellular calcium ion concentration. This in turn tends to reduce and shorten the ReP. Which effect dominates obviously depends on the conditions of the experiment: when the calcium concentration in the superfusate is reduced to ca. 40 Μmol/l a slow decrease of the ReP is accompanied by a small increase of the intracellular calcium ion concentration.
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  • 9
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    European biophysics journal 7 (1981), S. 205-208 
    ISSN: 1432-1017
    Keywords: Grasshopper ; Electroretinogram ; Adaptation ; Spectral sensitivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract The grasshopper ERG displays a rapid recovery of responsivity following the onset of a background light. Although observed earlier in skate and frog, this phenomenon has not previously been seen in an invertebrate. Furthermore, a period of hyperresponsivity exists in early dark adaptation and resembles that found in skate and frog. Thus, recovery in the light and hyperresponsivity in the dark seem to be corollaries of each other. Finally, spectral sensitivity of the ERG is determined and two peaks are found: one at 510 nm and the other at 360 nm. The former appears to be a rhodopsin-mediated sensitivity but the latter does not and they are not clearly separated by chromatic adaptation.
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  • 10
    ISSN: 1432-1017
    Keywords: Photoreceptor ; Visual pigment ; Adaptation ; Facilitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract A conditioning light can cause a decrease (adaptation) or an increase (facilitation) in the sensitivity of barnacle photoreceptors, as measured by the amplitude of the late receptor potential (LRP). We show that a net transfer of visual pigment from the rhodopsin (R) to the metarhodopsin (M) state induces a large facilitation whereas the reverse transfer results in a much smaller facilitation or even an adaptation. These effects were not due to the response to the conditioning light but to the pigment reactions. When the conditioning light did not alter the pigment population (i.e., M → M, R → R) it was followed by an intermediate degree of facilitation. These conclusions are correct for cells which have relatively low sensitivity. In sensitive cells, all pigment transitions produce adaptation. LRP facilitation and the prolonged depolarizing afterpotential (PDA) show several common characteristics with respect to pigment transitions: 1.Their magnitude increases with the amount of pigment transferred from R to M. 2. Both are depressed by the M → R transition. 3. Their production is impeded by the M → R transition. 4. The PDA itself is facilitated by the R → M transition and this facilitation decays with a time course comparable to that of LRP facilitation. These results suggest that there may be an underlying process common to LRP facilitation and PDA.
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  • 11
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    European biophysics journal 8 (1982), S. 173-187 
    ISSN: 1432-1017
    Keywords: Leech photoreceptors ; Extracellular calcium ; Excitation ; Adaptation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract Extracellular recordings from the vacoule of photoreceptor cells of Hirudo medicinalis L. were performed using microelectrodes. The cells were adapted by white light flashes given at constant intervals (20 s). Response height versus relative intensity curves obtained from the same cell in physiological saline (PS) and in bathing solutions of either a) lowered calcium contents (2 ΜM/1 or less) or b) raised calcium contents (15 mM/1) were compared. The cells' adaptation state in PS was operationally defined by the ratio Q=h A /h S where h A is the response height evoked by the adapting flashes, and h S is the corresponding saturation response height. Sensitivity changes were measured by the half saturation intensity shift. Lowering extracellular calcium resulted in: 1. The response height increased and the shape of the response became more rounded and prolonged. 2. The total resistance between the vacuole and outside decreased from 8.2±1.4 MΩ (n=6) in PS to 4.6±0.4 MΩ (n=5). The resistance was independent of the cells' adaptation state. 3. A change of the cells' sensitivity occured either in direction to light adaptation or in direction to dark adaptation. It depended functionally on the ratio Q: a) if Q was less or equal to about 0.6 the cells' sensitivity increased. b) if Q was greater than 0.6 the cells' sensitivity diminished. Raising extracellular calcium decreased the sensitivity of all cells tested independent of their adaptation states in PS. The results can be interpreted under the assumptions that 1. the sensitivity of leech photoreceptor cells is inversely proportional to the intracellular free calcium concentration and Z. intracellular calcium can interact with extracellular calcium in relatively dark adapted cells whereas in relatively light adapted cells the raise of intracellular free calcium is mainly effected by a release from intracellular stores. It is assumed that a Q value of about 0.6 separates relatively light adapted cells from relatively dark adapted cells.
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  • 12
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    Archives of microbiology 129 (1981), S. 127-128 
    ISSN: 1432-072X
    Keywords: Continuous culture ; Adaptation ; Simulation of hot springs ; Boiling point ; Caldoactive bacteria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Bacillus caldolyticus, a caldoactive bacterium originating from a hot spring at Yellowstone Park, was grown in a defined medium, whose composition resembled that of the pool water. Using a chemostat culture, which simulated the natural conditions, the organism could be adapted to grow at 100°C at a reasonable rate. Under increased pressure growth occurred also at 105° C.
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  • 13
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    Archives of microbiology 130 (1981), S. 159-164 
    ISSN: 1432-072X
    Keywords: Adaptation ; Boiling point ; Caldoactive enzymes ; Stabilization ; Thermostability ; Thermal characteristics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In chemostat cultures of Bacillus caldolyticus, adaptation in a single step from 70–100°C was followed under aerobic and oxygen-limited conditions and was found to proceed more smoothly under the latter circumstances. Variations of the medium (e.g. yeast extract or silicate concentrations) showed that growth at 100°C is in all respects similar to that of cultures at moderate temperatures. Enzyme preparations derived from cultures at 5°C intervals between 70 and 100°C were used to determine the temperature range. For all nine enzymes tested, the optimum temperature was found to be 67°C; the latter was independent of the growth temperature. Differences were found, however, with respect to the maximum temperature of individual enzymes, and three groups, with maxima between 70 and 80°C, 80 and 90°C and 90 and 100°C can be distinguished. Again, there was no correlation with the growth temperature. Stability experiments also revealed that enzymes from the same organism can have different thermal properties: Some were found to be quite thermolabile (e.g. the pyruvate kinase), while others (e.g. hexokinase and glutamate-pyruvate transaminase) exhibited a high thermostability. These properties were not related to the growth temperature within the 70–100°C range, too. Six of the enzymes tested could be stabilized by their respective substrates, but the degree of protection varied for individual enzymes. Three enzymes (acetate kinase, glutamate dehydrogenase and myokinase) could not be stabilized by their substrates. Comparative experiments with the hexokinase suggested, that the thermal integrity of the enzymes is better protected within the cell as compared to the stability of the enzyme preparations.
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  • 14
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    Archives of microbiology 131 (1982), S. 184-190 
    ISSN: 1432-072X
    Keywords: Dunaliella primolecta ; Malotolerant ; Adaptation ; Plasma membrane ; ESR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Electron spin resonance spectroscopy was used to monitor the in vivo microviscosity of the plasma membrane and lipid extracts of the salt tolerant alga, Dunaliella primolecta. The fluidity of the plasma membrane decreased as the algae were adapted to and suspended in higher sodium chloride concentrations [2–24% (w/v)]. Both biochemical modification and a physical interaction between Na+ and lipids were implicated. When the microviscosity of the plasma membrane and that of lipid extracts were determined as a function of temperature, two or three lipid phase transformations were observed. There were always transformations at 9–14° C and 39–43° C. These were interpreted as the onset and completion of the lipid phase transition of at least a major lipid component of the membrane, possibly the entire membrane. These transformation temperatures were independent of the salt concentration to which the algae were adapted or suspended. This suggests that D. primolecta exists with some of its membrane in the solid-fluid mixed lipid state. With a NaCl concentration of 8% (w/v) or greater in the growth medium, a third transformation occurred around 20–22° C. It was the result of a lipid-lipid interaction and was not related to adaptation.
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  • 15
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    Archives of microbiology 134 (1983), S. 204-207 
    ISSN: 1432-072X
    Keywords: Photosensory ; Cations ; pH ; Flagellated ; Algae ; Adaptation ; Euglena gracilis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Euglena were cultured under 3 W m-2 constant white light. In culture medium, cells show immediate and long lasting step-down photophobic responses and photoaccumulation behavior to blue light if dim red light-adapted for 30 min. However, if cells are suspended in buffered, saltcontaining solutions (adaptation buffers), strong step-down photobehavior and photoaccumulation responses are not observed for several hours. These behaviors gradually increase in strength to reach a maximum after 6–12 h; after which a stable response is maintained. The relative rates of appearance and the relative strengths of the responses are influenced by the concentrations of Ca2+ and K+, but not H+ or Na+ ions, in the adaptation buffers. Expression of the stepdown photobehavior thus requires that the cells adapt to the chemical environment in which they are suspended.
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  • 16
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Synechocystis 6701 ; Phycobilisomes ; Ultra-violet ; Mutagenesis ; Assembly ; Chromatic ; Adaptation ; Rods ; Cores
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Mutations affecting pigmentation of the cyanobacterium Synechocystis sp. 6701 were induced with ultraviolet light. Two mutants with phycobilisome structural changes were selected for structural studies. One mutant, UV08, was defective in chromatic adaptation and incorporated phycoerythrin into phycobilisomes in white or red light at a level typical of growth in green light. The other mutant, UV16, was defective in phycobilisome assembly: little phycocyanin was made and none was attached to the phycobilisome cores. The cores were completely free of any rod substructures and contained the major core peptides plus the 27,000 Mr linker peptide that attaches rods to the core. Micrographs of the core particles established their structural details. Phycoerythrin in UV 16 was assembled into rod structures that were not associated with core material or phycocyanin. The 30,500 Mr and 31,500 Mr linker peptides were present in the phycoerythrin rods with the 30,500 Mr protein as the major component. Phycobilisome assembly in vivo is discussed in light of this unusual mutant.
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  • 17
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    Archives of microbiology 140 (1984), S. 96-100 
    ISSN: 1432-072X
    Keywords: Physiology ; Adaptation ; Growth ; Droop ; Monod
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In many experimental ecological studies on phytoplankton species the growth response of an organism to the prevailing environmental conditions have been studied. Curves relating specific growth rate (μ) to the external nutrient concentration (S) have been constructed to compare nutrient-limited growth of different species under steady state conditions. Microorganisms adapt their physiology to a certain limitation in order to optimize growth. Therefore the shape of the μ/S curve is closely related to the way a micoorganism adapts its physiology. To see how physiological adaptation and growth rate are interconnected to each other, both can be related to the internal concentration of the growth-limiting nutrient. How the growth rate is related to the internal nutrient concentration is presented in a mathematical equation. Many phytoplankton species during growth under different nutrient limitations show a linear relationship between μ and the reciprocal value of the internal nutrient content (= Yield). This was originally observed by Droop. The model presented here gives a theoretical explanation of this phenomenon.
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  • 18
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    Theoretical and applied genetics 64 (1983), S. 133-136 
    ISSN: 1432-2242
    Keywords: Stability ; Adaptation ; Fitness trait ; Bunch yield ; Oil palm ; Elaeis guineensis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary There were significant differences between hybrids for number of bunches (NB), mean bunch weight (MBW) and fresh fruit bunch yield (FFB). For the hybrid population as a whole, significant hybrid X year (environment) effects were also observed for the two yield components and for yield per se. The linear component of the hybrid X year effect was also significant. There were highly significant and positive correlations between FFB, NB and MBW hybrid means and the regression co-efficients of the hybrid means on the environmental index. There were no significant associations between these means and mean square deviations from regression (s2d) for these traits.
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  • 19
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    Theoretical and applied genetics 66 (1983), S. 93-99 
    ISSN: 1432-2242
    Keywords: Lactation ; Milk yield ; Herd production ; Adaptation ; Dairy cattle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Eighty thousand, one hundred and eleven records of the Israeli dairy herdbook for the period of 1973–1977 were studied and examined to determine the existence of Genotype x Environment Interaction (GxE) as affecting milk yield in kg per day between calvings. Various quantitative measures of environment were used while the genotypes were evaluated as the average performance of each sire's daughters in a whole range of environments. When the environment was evaluated as level of production, the relative importance of the interaction was found to be very low. Furthermore, the linear dependence on the interaction of the individual sires with the environments was found to be inconsistent with time, meaning that no justification was found for using specific adaptation patterns of genotypes to these environments. When lactation number and given time periods were used as environments, significant interactions were found between genotypes and environments. Results of the analyses of Genotype x Lactation interaction imply that the interaction values, to a certain degree, confused the differences between the sires when based on first lactation records. We therefore conclude that the need exists to expand the basis of sire evaluation, including the addition of data on successive lactation periods beyond the first one. We maintain that the genetic characteristic for this phenomenon is the “lactations development” of a sire, i.e., the performance of its daughters during the different lactations. The “maturing rhythm” of a sire may be regarded as a dynamic expression of the genetic makeup controlling lactation development. Furthermore, the prospect of selecting sires of bulls for early or late maturing could provide a new tool for the dairy cattle breeder.
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  • 20
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    Theoretical and applied genetics 60 (1981), S. 145-149 
    ISSN: 1432-2242
    Keywords: Triticale ; Rye ; Hexaploids ; Adaptation ; Chromosomal substitutions ; Modified chromosomes ; Telomeric heterochromatin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Investigations were made on the rye chromosome constitution and on the presence of telomeric heterochromatin in rye chromosomes of the 26 most widely and 24 most narrowly adapted triticale strains. Among widely adapted lines, 22 (85%) had a complete rye genome and four triticales only had chromosomal R-D genome substitutions. Twenty-three (96%) of the 24 most narrowly adapted triticales had substitutions between the chromosomes of the R and D genomes. The most widely adapted triticales accumulated fewer modified rye chromosomes in comparison to narrowly adapted lines. They had from one to three rye chromosomes with heterochromatic deletions: 46% of widely adapted lines had two modified rye chromosomes; 34% had three modified rye chromosomes, and 19% had a single modified rye chromosome. In widely adapted strains, the 1R, 4R, 5R and 6R modified chromosomes were observed; they were present in 80%, 73%, 50% and 11% of the cases, respectively. The most narrowly adapted triticales had from two to four modified rye chromosomes: 58% of the strains had three modified rye chromosomes; 29% had four modified rye chromosomes and 12% had two modified rye chromosomes. The modified 4R and 5R chromosomes were present in all of these lines. The 1R (modified), 6R (modified) and 7R (modified) were found in 83%, 25% and 16%, respectively, of the narrowly adapted strains. Results support the previous observations (Pilch 1980b) that a wide adaptation of hexaploid triticales is associated with the presence of the full potential of rye genome, and that it is independent of the amount of telomeric heterochromatin possessed by rye chromosomes.
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  • 21
    ISSN: 1615-6102
    Keywords: Nickel ; Endocytosis ; Motility ; Proliferation ; Cellular nickel content ; Adaptation ; Tetrahymena pyriformis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary At concentrations above 1 mM, nickel has a dose-dependent effect on the rate of food vacuole formation in cells in the growth medium, proteose peptone (PP); total inhibition of endocytosis occurs within 10 minutes in 6mM nickel. However, only a 10 times lower concentration of nickel is tolerated by starved cells in an inorganic salt medium, a difference which may be ascribed to the high binding property of nickel to organic material. In the PP medium, nickel affects cell motility by increasing the rate of movement at a concentration of 1 mM, and by causing immobilization after 30 minutes in 6mM nickel; a spontaneous, partial recovery of cell motility is seen after 3 hours in 6 mM nickel. The effects of nickel on endocytosis and cell motility are reversible after removal of nickel. Cell proliferation continues at a reduced rate in 1 mM nickel, while only 1 1/2 cell doublings are achieved in 3 mM nickel during a 72-hour exposure, and no proliferation occurs in 6mM nickel, where an increasing cell mortality is observed after 12 hours. The cell content of nickel relates initially to the external concentration of the metal; however, cells in 1 mM nickel are capable of maintaining a constant content of the metal, whereas in 3 mM, the rate of accumulation is reduced after 3 hours, and cells in 6mM nickel accumulate the metal at a constant rate. All nickel-treated cells contain small refractive granules, previously proposed as representing an ion-regulating system, and the apparent adaption ofTetrahymena to the effects of nickel may be ascribed to such a regulation of the intracellular concentration of the metal.
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  • 22
    ISSN: 1615-6102
    Keywords: Adaptation ; Light intensity ; Ligustrum ; Plastids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The capacity of adaptation and the range of adjustment to different light conditions in fully expanded mutant leaves were studied on an aurea variety of privet (Ligustrum ovalifolium Hassk. var.aureum). Whenever the light conditions are altered leaves respond immediately. Although adaptational changes in leaf thickness are not possible, the change in colour, as well as changes in pigment concentrations take place within several days. With increasing light intensity there is a marked decline in chlorophyll concentration and the carotenoid yield becomes much higher. Under low light conditions the chlorophyll content is high, while the carotenoid concentration drops significantly. The mutant chloroplasts from green leaves always have a well developed thylakoid system. The only difference between young green leaves (DG1) and older regreened ones (DG2) is in the number of thylakoids per granum (grana in older leaves consist of more thylakoids), while the stacking degree of thylakoids remains about the same (74 and 77% respectively). Depending on the previous light conditions fine structure of plastids in yellow leaves differs considerably. Young yellow leaves (Y0) contain plastids with longitudinal arrays of dilated thylakoids and prothylakoid bodies occasionally. Plastids from primarily green leaves which turned yellow afterwards in strong sunlight (Y1) are characterized by thylakoids densely packed into cup-shaped stacks, or large vesicles originating from dilated thylakoids. The stacking degree of thylakoids in sun exposed yellow leaves (determined only in Y0 leaves) is extremely low and reaches only 29%.
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  • 23
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    Plant ecology 43 (1980), S. 83-86 
    ISSN: 1573-5052
    Keywords: Adaptation ; Colonization ; Environmental stochasticity ; Phenology ; Weather variation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Plant species co-inhabiting a given geographical region often have distinetly different times of flowering. It is shown that such phenological spread, duc to short-term stochastic variation in weather variables, relaxes competition for empty sites to be colonized by diaspores. For sufficiently large spreads stable coexistence becomes possible. The applicability of the proposed hypothesis to the observed instances of phenological spread is discussed and shown to extend beyond that of other current theories.
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  • 24
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    Plant systematics and evolution 143 (1983), S. 257-275 
    ISSN: 1615-6110
    Keywords: Angiosperms ; Poaceae ; Aegilops ; Triticum ; T. diccocoides ; wheat ; Adaptation ; trait variation ; factor analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Eighteen earliness and morphological traits were examined in from 2 to 14 lines each of 10 diploid members of the wheat complex,Triticum-Aegilops, and 15 lines of the tetraploid speciesTriticum diccocoides. In general, earliness traits have the greatest relative between line vs. within line variation of all the traits examined. Within species, earliness traits are the principle set of characters around which evolve between line trait differences, one of the most important oich is leaf dimensions. At the genus level, earliness traits are independent of leaf dimensions and plant height characters. Thus, the pattern of evolution at the genus level is different from that exhibited in each of the species. Biological and evolutionary implications of these findings are discussed.
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    Plant and soil 61 (1981), S. 43-52 
    ISSN: 1573-5036
    Keywords: Adaptation ; Allelopathy ; Ecophysiology ; Grassland ; Plantago ; Nitrate production ; Nitrate reductase ; Nitrate uptake ; Nitrification ; Nitrifying bacteria ; Rhizosphere ; Root environment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The production of nitrate in an old established dune grassland soil and its uptake by plants was studied by comparing amounts of mineral nitrogen and numbers of nitrifying bacteria in the rhizosphere on the one hand, and on the other accumulated nitrate and levels of nitrate reductase (NaR) of individual plants of three Plantago species,i. e., P. major, P. lanceolata andP. coronopus. For these three Plantago species andP. media basal levels of NaR in the absence of nitrate were determined in plants grown in culture solutions. The basal NaR levels ofP. major andP. media (species occurring on nutrient-rich soils) were significantly higher than those ofP. lanceolata andP. coronopus (species found on nutrient-poor soils). NaR activity increased in the presence of nitrate and was suppressed by ammonium. From the numbers of nitrifying bacteria in the rhizosphere and NaR activity in the leaves it was concluded that nitrate was produced in the root environments of the three Plantago species and that the compound was taken up by the plants. NaR activities and numbers of nitrifying bacteria were higher for individuals ofP. major than for those ofP. lanceolata andP. coronopus. No correlation was found between the ammonium levels and the numbers of nitrifying bacteria in the soil, and no indications of inhibition of nitrifying bacteria in the rhizosphere were obtained. For individuals ofP. lanceolata a correlation was found between the numbers of nitrifying bacteria in the soil and NaR activity in the leaves. The results are discussed in relation to the ecological habitats of the three species.
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    ISSN: 1573-5036
    Keywords: Adaptation ; Luzerne ; Mutant ; Rhizobium meliloti ; Terres acides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Resume Un mutant acido-tolérant deR. meliloti a été isolé. Le caractère de résistance en milieu acide n'a pas été obtenu par adaptation sur des milieux de plus en plus acides mais par mutagenèses successives provoquées par la N-méthyl-N'nitroso-N-nitrosoguanidine (NTG) et sélection sur milieu acide de façon à rendre stable le caractère acido-tolérant. Ce mutant acide présente la propriété de se développer plus lentement que la souche sauvage sur milieu pauvre. Ceci ne l'empêche pas de présenter sensiblement la même efficience que cette dernière à pH voisin de la neutralité en milieu synthétique. L'étude comparative de l'efficience de la souche parentale et de la souche mutée sur la luzerne cultivée en terre acide est rendue difficile du fait de la présence de nitrates qui réduit la nodulation et inhibe l'action de la nitrogénase: par épuisement, en effectuant une culture dense de luzerne sur cette terre, il est possible de mettre en évidence ensuite l'activité symbiotique importante à pH 5,9 du mutant par rapport à la souche sauvage.
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  • 27
    ISSN: 1573-5036
    Keywords: Adaptation ; Adventitious roots ; Ethylene ; Flooding ; Fraxinus pennsylvanica ; Lenticels ; Turgidity ; Water potential ; Water relations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Fraxinus pennsylvanica Marsh. seedlings that were 150 days old adapted well to flooding of soil with stagnant water for 28 days. Early stomatal closure, followed by reopening as well as hypertrophy of lenticels and formation of adventitious roots on submerged portions of stems appeared to be important adaptations for flood tolerance. Leaf water potential (ψ1) was consistently higher in flooded than in unflooded seedlings, indicating higher leaf turgidity in the former. This was the result of (1) early reduction in transpiration associated with stomatal closure, and (2) subsequently increased absorption of water by the newly-formed adventitious roots as stomata reopened and transpiration increased. Waterlogging of soil was followed by large increases in ethylene content of stems, both below and above the level of submersion. Formation of hypertrophied lenticels and adventitious roots on flooded plants was correlated with increased ethylene production. However, the involvement of various compounds other than ethylene in inducing morphological changes in flooded plants is also emphasized.
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    Plant and soil 66 (1982), S. 243-255 
    ISSN: 1573-5036
    Keywords: Adaptation ; Adventitious roots ; Ethylene ; Flooding ; Growth of seedlings ; Lenticels ; Platanus occidentalis ; Stomatal aperture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Flooding ofPlatanus occidentalis L. seedlings for up to 40 days induced several changes including early stomatal closure, greatly accelerated ethylene production by stems, formation of hypertrophied lenticels and adventitious roots on submerged portions of stems, and marked growth inhibition. Poor adaptation ofPlatanus occidentalis seedlings to soil inundation was shown in stomatal closure during the entire flooding period, inhibition of root elongation and branching, and death of roots. Some adaptation to flooding was indicated by (1) production of hypertrophied lenticels which may assist in exchange of dissolved gases in flood water and in release of toxic compounds, and (2) production of adventitious roots on stems which may increase absorption of water. These adaptations appeared to be associated with greatly stimulated ethylene production in stems of flooded plants. The greater reduction of root growth over shoot growth in flooded seedlings will result in decreased drought tolerance after the flood waters recede. The generally low tolerance to flooding of seedlings of species that are widely rated as highly flood tolerant is emphasized.
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    Environmental biology of fishes 5 (1980), S. 191-224 
    ISSN: 1573-5133
    Keywords: Adaptation ; Benzidine stain ; Catostomid ; Discontinuity theory ; Ecomorphology ; Embryology ; Fish ; Haemoglobin stain ; Hatching ; Peroxidase ; Thresholds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Synopsis Frequent and detailed observations of arbitrary stages revealed a saltatory pattern of development in the early ontogeny of fluvial spawning white sucker. Considered as adaptations for respiration were: i) expansion of the surface area of the yolk through a change in yolk shape, ii) the presence of carotenoid pigment in the yolk, iii) a large caudal vein sinus, iv) coverage of the yolk surface with capillaries of bilaterally paired vitelline plexi, and v) a large pair of vitelline veins. The ability to swim developed slowly and well after hatching. Young suckers would therefore spend most of the eleutheroembryonic phase in the interstices of the rock substrate of the spawning ground. The change from a benthic to pelagic mode of existence occurred with swimbladder inflation and before the start of exogenous feeding.
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    Cell & tissue research 221 (1981), S. 209-220 
    ISSN: 1432-0878
    Keywords: Liver (Rat) ; Organelle topography ; Adaptation ; Fructose ; Quantitation ; Histochemistry ; Morphometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary After seven days of feeding fructose the liver of Wistar rats showed enormous accumulations of glycogen, which completely altered the original pattern of distribution of organelles. A quantitative morphological method was used to analyze these changes. The cytoplasm was mapped into arbitrary “distance classes” corresponding to concentric rings beginning at the outer nuclear membrane. This allowed the density of organelles in a given zone to be estimated. In cells filled with glycogen as a result of the fructose feeding, the following rearrangements were found: in the intermediate zone of both cellular poles (i.e., bile canalicular pole and sinusoidal pole) the mitochondria disappeared, being replaced by glycogen. The endoplasmic reticulum was accumulated in the perinuclear zone of both cellular poles, as in control animals, but was reduced throughout the rest of cytoplasm. It showed a peripheral density maximum at the biliary canalicular pole, in contrast to the cells of control animals. These changes in the distribution of the organelles and cellular “compartments” correspond to histochemical findings and demonstrate an adaptive reaction in the liver parenchyma to fructose ingestion, the organelles arranging themselves in cytoplasmic regions which still show a metabolic activity.
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    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1125-1136 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric relaxation of polyacrylonitrile (PAN) samples, in which the presence of an amorphous phase is evidenced by x-ray diffraction, has been studied over the temperature range 30-150°C and frequency range 102-105 Hz. These data as well as those reported by other authors, reveal several points useful to the understanding of the dielectric relaxations of PAN in relation to its structure. A glass transition in PAN is evidenced by at least two of the four data sets investigated; the third shows combined effect of two relaxations, whereas the fourth clearly shows a relaxation process different from the glass transition. The glass-transition behavior of the dielectric relaxation data is confirmed by Williams-Landel-Ferry theory and a recent theory of Phillips, both of which lead to consistent conclusions.
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    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1175-1186 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The flexibility of some polyimide chains has been studied theoretically as a function of the chemical structure of the repeat unit. It has been shown that the thermodynamic flexibility can be varied over a wide range by the choice of the unit structure. For three polyimides, as an example, the flexibility of cyclochain structures approximates that for free rotation.
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    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1237-1242 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron microscopy reveals a high-temperature morphological transition in a styrene-butadiene-styrene block copolymer of 7000 polystyrene block molecular weight and 43,000 polybutadiene block molecular weight (7S-43B-7S). Samples quenched in liquid nitrogen from temperatures above 150°C show no structure, whereas those quenched from temperatures below 140°C clearly show a multiphase structure. We previously reported that the 7S-43B-7S polymer exhibits a relatively sharp melt rheological transition in the temperature region between 140 and 150°C from highly viscoelastic and nonlinear viscous behavior to linear viscous behavior with insignificant elasticity. The dynamic viscoelastic properties are measured at different strain amplitudes in this study, and the results show that the melt rheological transition behavior is not influenced by the strain amplitude. This study clearly shows that the melt rheological transition in the 7S-43B-7S results from a morphological transition from a multiphase structure below about 140°C to a single-phase structure above about 150°C.
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    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1103-1124 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model of simple molecule sorption in polymers is proposed which embraces both the glassy and rubbery regions, and incorporates the successful dual-mode model below the glass-transition temperature. Hole filling is shown to be an important sorption mechanism both above and below Tg, although saturation effects do not occur in the rubbery polymer. The model interprets the “dual-mode” Langmuir and Henry's law parameters at the molecular level, and a simple statistical mechanical analysis allows estimation of the parameter values, as well as specifying certain interrelationships between the parameters. Applications of the model to gas solubility data in five polymers are considered [polyethylene (PE), poly(ethylene terephthalate) (PET), polystyrene (PS), polymethacrylate (PMA), poly(vinyl acetate) (PVAc)] and semiquantitative agreement is obtained for PE, PET, and to a lesser extent, PS. For PMA and PVAc, the agreement is qualitative only.
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    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-angle x-ray relaxation studies were performed on films of low- and high-density polyethylene (PE). The samples were rapidly stretched by a pneumatic stretcher and held at a fixed length. The rate of crystal reorientation was monitored by measuring diffracted intensity changes using a count-rate meter with output displayed on a storage oscilloscope as well as a digital counter-timer. Experiments were completed at several temperatures and activation energies comparable to those reported for the α1 relaxation in PE were obtained.
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    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Homogeneous catalytic systems based on optically active low-molecular-weight and macromolecular titanium alcoholates and tri-isobutyl aluminum were used in the isomerization and hydrogenation of chiral and prochiral olefins. The reactions performed in a nitrogen and hydrogen atmosphere show a different behavior in regard to reaction rate, composition of reaction mixture, and stereochemical control. The catalyst based on macromolecular titanium alcoholate displays lower activity and a varying influence on the stereochemical pathway with respect to the catalysts based on low- molecular-weight alcoholates. The data obtained in both cases strongly support the absence of a stereocontrol by the growing chain in the stereoelective polymerization of racemic α-olefins by Ziegler-Natta catalysts based on optically active precursors. Finally evidence is provided in favor of the intermediate step responsible for asymmetric isomerization which does not occur via η-allyl complex.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2461-2470 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general detailed model of polymer oxidative degradation in the presence of a stabilizer-oxygen acceptor was considered. The motion of the degradation zone boundary and the sample lifetime were obtained for various conditions of the process. In particular, it is shown that within the given concentration immobile oxygen acceptor has the best stabilizing properties. The theoretical results are compared with the experimental data obtained by using two independent methods: polymer sample cracking and a change in the ESR signal. Good agreement between theory and experiment was obtained.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2197-2207 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical polymerization and copolymerization of some o-alkylphenyl methacrylates were carried out and the effect of the ortho-substituents on the ability to homopolymerize, on the monomer reactivities, and on the ceiling temperatures of the monomers was studied. The effect of the substituent on tacticities and thermal stabilities of the polymers formed was also discussed. The ability to honiopolymerize and the monomer reactivity were considerably decreased by the introduction of the o-substituent. 2,6-Di-tert-butylphenyl methacrylate formed no methanol-insoluble polymer at 60°C. On the basis of the tacticity determined it was noted that the o-substituted phenyl methacrylates preferred syndiotactic addition in the propagation reaction less than did phenyl methacrylate or methyl methacrylate. The polymers formed from the o-substituted monomers were thermally less stable than poly(phenyl methacrylate), and, consistent with this finding, ceiling temperatures of the o-substituted phenyl methacrylates seemed to be lower than that of phenyl methacrylate. The effects observed were characteristic of the o-substituents conformationally close to the carbon-carbon double bond of the monomer or the carbon carrying the unpaired electron of the polymer radical.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2239-2246 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolymerization of acrylonitrile (r1) and p-acetoxystyrene (r2) in bulk yields reactivity ratios r1 = 0.08 and r2 = 0.42. Crosslinked resins are readily obtained by a new type of precipitation copolymerization of acrylonitrile, p-acetoxystyrene, and divinylbenzene. After deacetylation, the phenolic groups afford useful attachment sites for protected amino acids as a first stage in solid-phase peptide synthesis. Reactivity of typical 10% functionalized polyacrylonitrile-based resins is comparable to that of the more usual polystyrene-based equivalents, although swelling characteristics of the two types of resin are very different.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2281-2291 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Macosko-Miller approach is used to obtain an expression for the polydispersity index for AA, BB, CC linear step polymerization system in which B and C are the same type of functional group. The dependence of the polydispersity index, as a function of the extent of reaction, on the monomer masses and on the relative reactivities of B and C groups toward A, is examined in detail.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2307-2322 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The various kinds of molecular defect that are related to the thermal property of polyacrylonitrile (PAN) are studied in detail in relation to the polymerization mechanism in an aqueous medium. The existence of two different kinds of polymer radical is pointed out and the significance of polarity of radical species is emphasized. It is shown that the structural irregularity along the main chain is surely present but has little effect on the thermal property of PAN. It is estimated that one of the most significant defects relating to the thermal property is the main-chian type of branching the occurs predominantly in hydrogen on a polymer backbone. The relationship between activator (i.e., NaHSO3) incorporation and branch inhibition mechanisms is discussed. The optimum polymerization condition, under which the highest thermal quality of molecules is obtained, is found empirically within a limited experimental range, for an aqueous heterogeneous system.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2333-2346 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of chloromethylated polystyrene with methyl(2- hydroxyethyl)amine and butyle (2-hydroxyethyl)amine was studied kinetically. The reaction of benzyl chloride with these amines was also investigated for comparison. N,N-dimethylformamide and dioxane were used as solvents. The reactions of benzyl chloride with the two amines in these solvents took place according to normal kinetics of the second order. Reaction kinetics depend on the nature of the amine and solvent in Chloromethylated polystyrene reactions. In dioxane the self-accelerating effect of the reaction for β ≃ 0.5 is apparent. Steric hindrance of the reaction, beginning with a conversion degree of about 75%, wss observed for butyl(2-hydroxyethyl)amine in N,N-dimethylformamide. This self-accelerating effect is observed in dioxane at the same reaction degree. The activation energies and frequency factors were calculated for the amination of benzyl chloride and chloromethylated polystyrene with the two amines in N,N-dimethylformamide and dioxane.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2391-2410 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Methyl-5-vinylpyridine-N-oxide, 4-vinylquinoline-N-oxide. 9-vinylacridine-N-oxide, p-N,N-dimethylaminostyrene-N-oxide units were introduced in polymeric chains as homopolymers or/and as styrene copolymers to study their photocrosslinking. The method used for characterization of photocrosslinked films was a “photoresist test” described in Part I of this series. The photosensitivity of the different chromophores bound to the different polymer has also been studied by UV, IR, and fluorescence spectrophotometries. The use of aromatic amine N-oxide groups in polymers seems to be a general means to produce their photocrosslinking by radical reactions. Among the different polymeric materials prepared, 4-vinylpyridine-N-oxide and 4-vinylquinoline-N-oxide are the most photosensitive.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2437-2449 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymorphic behavior and γ-ray-initiated postpolymerization of the even-numbered long-chain Methacrylates (C18-C12) have been investigated. Phase transition behaviors of octadecyl, hexadecyl, tetradecyl, and dodecyl methacrylates are respectively, which become simpler with shortening of the chain length. The methacrylate monomers with sufficiently long hydrocarbon chains, such as octadecyl and hexadecyl, can be polymerized rapidly in the α-form crystal (hexagonal packing) by a fully two-dimensional mechanism, whereas in the β-form crystal (triclinic packing), polymerization can hardly occur. In the case of dodecyl methacrylate, however, an accelerated polymerization in the β form occurs after an induction period of several hours and the resultant polymer is gel-like. This can be interpreted by the propagation reaction across the polymer chain already formed. It has been found that the solid-state post-polymerization of n-alkyl methacrylates is affected by the chain length through the packing mode of the monomer molecules and also by the aggregation state of side chains in the resultant comblike polymer.
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  • 45
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: The effect of epoxy groups at the surface layer of ethyl acrylate-glycidyl methacrylate copolymer (1) emulsion particles on its crosslinking reactivity has been investigated. For this purpose two series of I emulsions were prepared. In the Y series, of which emulsion particles have epoxy groups at the surface layer, the epoxy content in the polymerization recipe was varied. For preparing the X series, of which emulsion particles have few epoxy groups at the surface layer, the high epoxy content of a given emulsion was reduced by various degrees of cleavage reaction with HCl-CaCl2. In emulsion blend films with amine-group-containing copolymer (II) emulsion, where the crosslinking reaction was expected to proceed only at the interfacial layer of I and II emulsion particles, the Y series, compared to the X series at the equal overall epoxy content in particles, showed less swelling and higher gel fraction in dioxane, less swelling in water, and higher tensile strength and modulus. On the other hand, this difference was not observed in the next two crosslinked films in which crosslinking was expected to be homogeneous. First, blends of I and II, which were isolated from the corresponding emulsions discussed above, were cast from dioxane solutions. Second, I emulsions were cast with BF3 ether complex which was expected to penetrate into the particles. It is concluded that the response of I emulsion cleaving the epoxy groups at the surface layer of particles to subsequent interfacial crosslinking is obviously reduced. However, even such an emulsion can be crosslinked to an extent similar to that of an uncleaved emulsion with similar overall epoxy content, if the crosslinking reaction is conducted so as to give an homogeneous effect.
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Ammonia used as both reactant and solvent has been shown to dehydrochlorinate 1,1,1-tri-chloro-2,2-bis(4-hydroxyphenyl)ethane smoothly to 1,1-dichloro-2,2-bis(4-hydroxyphenyl)ethylene. The reaction is complete in 1 hr at 100°C, and after two crystallizations from methanol/water affords polymerizable quality monomer for the synthesis of highly flame-resistant polycarbonates. The use of organic solvents in combination with ammonia does not offer any rate advantages over pure ammonia. Primary and secondary amines also can be used to effect the dehydrochlorination but, except for the methylamine, are significantly less reactive and lead to less pure product than amonia.
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  • 47
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2513-2521 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of p-benzoquinone with tin tetrachloride in the absence of solvents was investigated by isolation and identification of the reaction products. This reaction leads to the formation of polymeric quinone-tin derivatives free from combined chlorine, chlorinated quinones, quinhydrone, and minute amounts of CI2 and HCI gases. The tin content varies accroding to the molar ratios of the reactants and reaches its maximum (72%) at the smallest SnCI4 ratio. The existence of the Sn-Sn bond in the polymeric derivatives was confirmed chemically and spectroscopically. A mechanism based on the formation of radical intermediates which can account for the reaction products was developed. In view of their quinonoid nature, high thermal stability, and the presence of Sn-Sn bonds, the polytin derivatives are to be investigated as radical traps in the stabilization of polymeric arcticles against radical degradation process.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2523-2533 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymeric p-benzoquinone-tin derivatives obtained from the reaction of p-benzoquinone with tin tetrachloride in the absence of solvent have been investigated as thermal stabilizers for rigid PVC at 200°C by measuring the rate of dehydrochlorination. The results reveal the greater stabilizing efficiency of the investigated products in relation to dibutyltin maleate and the basic lead stabilizers commonly used in industry. Evidence has been accumulated that the quinone and metallic elements (Sn—Sn bonds) of the stabilizer participate in the stabilization process by trapping the radical intermediates of degradation and blocking the odd electron sites formed on the polymer chains. Although stabilizers with high quinone content provide greater stabilization in the early stages of degradation, their efficiency sharply decreases in subsequent stages. On the other hand, stabilizers of high tin content effectively prohibit the dehydrochlorination reaction at all stages of degradation. On an equivalent basis of metal content, the results clearly demonstrate the greater stabilizing efficiency of tin atoms when found in direct contact in the stabilizer molecule. The mechanism of stabilization suggested to account for the results obtained may be considered as additional evidence in support of the radical nature of the dehydrochlorination reaction.
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  • 49
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2577-2583 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Availabilities of O(3)H relative to O(2)H (that is, [O(3)H]a/[O(2)H]a) on accessible surfaces of microstructural units of cotton fibers were measured by chemical microstructural analysis (CMA). CMA involves a mild chemical reaction with N,N-diethylaziridinium chloride, determination of substituent distribution for this product and a corresponding product from decrystallized cellulose, and simple computations. Measurements for fibers in commercial cotton fabric, for field-dried fibers, and for never-dried fibers are reported. The [O(3)H]a/[O(2)H]a, an inverse measure of intact O(3)H ·· O(5′) bonds, decreased in the stated order; thus, intact O(3)H ·· O(5′) hydrogen bonding increased in this same order. Results indicate a high degree of order in intramolecular bonding in the never-dried fiber and an increasing disruption of this bonding as the never-dried fiber is dried and processed.
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  • 50
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2597-2608 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mixtures in various proportions of natural rubber (NR) and each of two tackifier resins, a poly-β-pinene and a modified pentaerythritol rosin ester, were used as the adhesive layer in joining a flexible polyester strip to a plane glass substrate. Measurements of the force required to peel the strip from the glass at a 90° angle were made over a range of pulling rates at several temperatures. Application of time-temperature superposition enabled a master curve of (reduced) peel force versus (log) pulling rate at a standard temperature (296 K) to be obtained for each adhesive composition. The master curves showed, in increasing order of pulling rate, some or all of four different modes of peeling: (i) peeling with viscous adhesive response, (ii) peeling with rubbery response, (iii) oscillatory or slip-stick peeling, and (iv) peeling with glassy adhesive response. In general, transitions between the different peeling modes were quite abrupt. Increase in concentration of tackifier resin caused displacement of the master curve toward lower pulling rates [an effect interpreted in terms of an increasing adhesive glass temperature (Tg)], and a superimposed displacement of the transition between peeling modes (i) and (ii) toward higher pulling rates-an effect attributed to reduction in adhesive average molecular weight. The influence of the tackifier resin in modifying the viscoelastic characteristics of the adhesive was further demonstrated in a comparison of the peel force master curves with corresponding master curves of dynamic storage modulus.
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  • 51
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2641-2648 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phase diagrams for monomer (methyl acrylate containing microemulsions) are shown and described. Polymerizations of a series of microemulsified monomer reveals the expected linear dependence of 1/DS vs. [S]/[M] for pentanol acting as a chain transfer agent and giving a value of 5.1 × 10-4 for Cs. No break in molecular weight behavior was shown as a result of micellization at higher water contents. A comparison of molecular weights obtained by various classical methods (solution, emulsion, bulk) are also given.
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  • 52
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2663-2676 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Soluble tricarbonylchromium complexes were made by reacting Cr(CO)6 with a ladder polyphenylsilsesquioxane and a linear polydiphenylsiloxane. These new polymer Cr(CO)3 complexes were characterized by elemental Cr, infrared (IR), gel permeation chromatography (GPC), viscosity, and thermal analyses and were evaluated as stereoselective hydrogenation catalysts. Thermogravimetry studies demonstrated that the new complexes were more stable at 180-200°C in N2 than the corresponding complex from crosslinked polystyrene. These silicone polymer complexes catalyzed stereoselective hydrogenation of methyl sorbate to cis-3-hexenoate in cyclohexane and tetrahydrofuran (THF) and could be recovered from THF for recycling by precipitation-fiItration. Catalytic activity and recyclability, however, were highly influenced by the solvent. Loss of catalytic activity associated with loss of Cr(CO)3 was observed on recycling. These results support a mechanisim that involves dissociation of Cr(CO)3, a significant portion of which cannot become reassociated with the polymer phenyl groups.
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  • 53
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2723-2729 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mild, efficient method of nitrating olefins was described recently by Corey and Estreicher. Application of their procedure to diene polymers failed because of the insolubility of the hydrophobic polymer in the aqueous nitromercuration regent. Use of water-immiscible organic cosolvents gave slow nitromercuration with substantial formation of nitrite esters. To overcome these problems a nonaqueous phase transfer-assisted method of rapid selective nitromercuration of diene polymers was developed.
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  • 54
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2737-2746 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Blends of polystyrene and poly(2,6-dimethyl-1,4-phenylene oxide) that cover the entire compositional range have been subjected to the action of singlet oxygen from microwave discharge, dye-sensitized reaction, and photochemical oxidation. With the applied analytical technique, which consisted of infrared (IR) analysis, including ATR technique and a spectroscopic method combined with chemical analysis for hydroperoxide groups, it was not possible to detect any effect of the singlet oxygen treatment. For that reason singlet oxygen does not appear to be important to the initiation of the photooxidation of these blends. In connection with photochemical oxidation the interaction observed between the two components probably involves energy transfer from PS to PPO. This interaction results in the enhancement of reactions in PPO that lead to greater carbonyl group formation and crosslinking. Simultaneously, the probability of chain scission in the PS is lowered with increased PPO content, found by determining the changes in the molecular weights.
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  • 55
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2773-2784 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced cationic polymerization of ethyl and isopropyl vinyl ethers was studied in a variety of solvents. The propagation rate constants were estimated and found to vary widely with the nature of the solvent. In particular, a good linear relationship existed between the logarithms of the rate constants and the reciprocal of the dielectric constants. The lowest rates were those of the highest dielectric constant solvents. These results have been interpreted in terms of the Laidler and Eyring theory of ion-molecule reactions. Isopropyl vinyl ether polymerizes much faster than ethyl vinvl ether, although the rates approach the same value at infinite dielectric constant. In contrast, “free” carbenium ion polymerizations initiated by stable carbenium ion salts in methylene chloride solution had similar values for both monomers. A comparison is made between the rate constants obtained with both methods of initiation.
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  • 56
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2793-2802 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Lipoic acid was immobilized on crosslinked polystyrene beads to generate a polymeric reagent. The acyl transfer reaction of the p-nitrobenzoyl group from the polymer-bound lipoic acid to cyclohexylamine was investigated spectrophotometrically and was compared with a monomeric model compound. The acceleration effect of silver ion on the acyl transfer reaction also was studied.
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  • 57
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2811-2821 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of soapless emulsion polymerization is studied experimentally and theoretically. The soapless emulsion polymerization of methyl methacrylate (MMA) in water is carried out with potassium persulfate as initiator. It is shown that the soapless emulsion polymerization of MMA gives different time-conversion and time-average molecular weight curves from those of bulk and emulsion polymerizations. Comparing the experimental results with those of the other types of polymerization, features of the rate of soapless emulsion polymerization are discussed and a kinetic model is proposed to apply the soapless emulsion polymerization of MMA in water. The experimental results can be well expressed by this model.
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  • 58
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2857-2866 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermally activated ethylene polymerization catalysts which contain chromium and titanium on silica differ from those catalysts which contain only chromium on silica. The characteristics of chromium-titanium catalysts vary with the method of incorporating the titanium and the thermal activation procedure. Titanated catalysts of the kind examined in this article have faster initiation and a higher polymerization rate per unit catalyst weight than corresponding catalysts without titanium. High-density polyethylene produced by this type of titanium-chromium catalyst tends to have a higher melt index and a broader molecular weight distribution than polyethylene made with chromium on silica catalysts. Iodometric titration showed that reduction from the initial hexavalent chromium to trivalent occurs when the dry, catalyst starting material is treated with titanium tetraisopropoxide. A study of the reaction between chromium trioxide and titanium tetraisopropoxide in carbon tetrachloride revealed that (1) it is not necessary to have a reaction between surface silanols and titanium tetraisopropoxide for the reduction to occur, and (2) the reaction product has an absorption near 660 nm in the visible range. Comparison of spectra showed that chromium trioxide on silica reduced by isopropyl alcohol has a shifted absorption, i.e., 600 nm. These findings are interpreted to mean that titanium atoms come sufficiently close to chromium atoms to change their electron density in the starting material and remain close neighbors in the activated catalysts. The interpretation is further supported by ESCA data and leads to the proposal that in this case the activated catalysts contain titanium chromate structures.
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  • 59
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3059-3067 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formation of two kinds of solvation complex of poly(ethylene oxide), polydimethoxyethylene, and polydioxene with some alkali derivatives of fluorene in dioxane was found, differing in the ionic species of the fluorenyl metal in the complex. Additional evidence was found for the existence of peripherally solvated ion pairs of fluorenyllithium, -sodium, and -potassium. It was shown that polydimethoxyethylene and polydioxane interact with different cations in a different manner. The complexing ability of poly(ethylene oxide) and polydioxane with respect to fluorenyllithium, -sodium, and -potassium, and of polydimethoxyethylene for fluorenyllithium, was proved to be stronger than that of their monomer analogs - dimethoxyethane and dioxane. This was explained by the effect of the polymer chain.
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  • 60
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3089-3099 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Configuration rules were established for the polymerization of cyclic monomers with chiral initiators. The latter recognize in the monomer an asymmetric carbon of homochiral configuration. The chirality of the initiator is defined by the “local” asymmetry of the ligand and by the overall asymmetry of the particular arrangement of catalytic aggregates. Two types of process called “homosteric” and “antisteric,” which apply to the polymerization of resolvable monomers and achiral monomers of meso structure, are defined. These configurational rules have a general character and are verified in many examples of differently substituted three- or four-membered cyclic monomers (oxiranes, thiiranes, β-lactones). Stereoelective polymerization appears to be an original method for the determination of the absolute configuration of some monomers of unknown chirality.
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  • 61
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 9-25 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: PVC has been cyclopentadienylated by two conventional basic, LiCp and NaCp, and a new acidic, Me2CpAl, cyclopentadienylating agent. PVCs treated with basic cyclopentadienylating agents undergo severe random dehydrochlorination and exhibit a significant decrease in thermal and thermooxidative stability. In contrast, according to ozonization and degradation experiments, Me2CpAl does not cause dehydrochlorination during cyclopentadienylation. The thermal stability of PVC treated with relatively high concentrations of Me2CpAl and Me3Al at 25°C markedly increases due to substitution of labile chlorines in PVC with methyl groups. Initial thermal dehydrochlorination behavior of virgin PVC and samples treated with Me2CpAl at -30°C are similar. In contrast, thermooxidative stability decreases on Me2CpAl treatment at -30°C; this is attributed to ease of oxidation of pendant cyclopentadienyl groups; that is, the formation of peroxy radicals that may initiate dehydrochlorination by attacking unchanged repeat units in PVC. Acceleration of thermal dehydrochlorination disappears and the length of polyene sequences is reduced on Me2CpAl and Me3Al treatment. These observations are attributed to differences in rates of protonation-deprotonation; that is, rates of reinitation of zipping of treated and untreated PVCs during thermal degration. The effect of traces of aluminum residues on degradation of modified PVCs, however, cannot be neglected.
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  • 62
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 65-72 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Chloro- and lithio-terminated diorganosilylene oligomers were coupled to form block copolymers that were soluble in common solvents and deposited coherent films from solution. Copolymer UV (ultraviolet) spectra showed a red shift in absorption maxima attributed to increased silicon chain length and phenyl-silicon spine interactions.
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  • 63
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 89-101 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Poly(p-phenylene) was alkylated with n-propyl bromide, n-propyl chloride, and isopropyl bromide in the presence of aluminum chloride. Apparently, the reactions involve dialkylation with n-propyl halides and alternating mono- and dialkylation with isopropyl bromide. Alkylation with ethyl or n-butyl bromide was unsuccessful. The dialkylated polymer was sufficiently soluble to allow molecular weight determination. Mechanistic aspects of alkylation and propagation are treated.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 115-126 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of poly(vinyl alcohol) (PVA), a steric stabilizer, and sodium dodecyl sulfate (SDS), an electrostatic stabilizer, on the stability of styrene dispersion polymerized systems was studied. It was shown that in stabilization by PVA there was pronounced bridging of the submicron emulsion particles to 10-μ dispersion particles and that the emulsion particles could not be washed off. In SDS stabilization, on the other hand, the emulsion formed was easily washed off because bridging with SDS does not occur. The surface tension of the aqueous phase measured during polymerization showed different characteristics for stable and unstable systems.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 213-215 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3307-3310 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3289-3296 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heterogeneous or homogeneous polyelectrolyte influences on the solvolyses of t-butyl chloride and α-phenethyl chloride were studied. Anionic polymers enhanced the reaction rate by stabilizing the intermediate point dipole (ionic strength effect); cationic polymers with chloride ions as gegenions retarded the reaction by the mass action law (common ion salt effect), thus supporting the theory of Ingold et al. On the other hand, neutral polymer resins retarded the reaction probably because of the binding of the substrate on the resin surface. By the addition of a neutral polymer resin. Amberlite XAD-4 the net steric course of the solvolysis of α-phenethyl chloride was slightly changed from inversion to racernization, whereas anionic resins (Amberlite IR-124) showed no effect. The heterogeneous polymer resin effect on the dearnination of α-phenethyl amine was also studied. An anionic resin (IR-124) retarded the reaction slightly and a neutrai resin (XAD-4) retarded it to a great extent. A cationic resin (Dowex 1 × 8) accelerated the reaction, although slightly. The net steric course of the deamination was changed from inversion to racemization in the order XAD-4 〉 Dowex 1 × 8 〉 IR 124. The heterogeneous polymer effect of the stereochemistry depended mainly on the hydrophobicity: i.e., the ability to bind the substrate on the surface of resin.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3297-3305 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bulk polymerization of chloroprene was studied at 25°C in a wide does rate range. Variations of the rate of polymerization (Rp) and molecular weight as a function of does rate were essentially the same as those in several monomers that are capab;e of radical and cationic polymerizations. The polymerization proceeds with radical mechanism at low dose rate ans with radical and cationic mechanism concurrently at high dose rate. The number-average molecular weight of the high-dose-rate was ca. 2400. Microstructure of the polymers was mainly of trans-1,4 unit with small fraction of cis-1,4 and 3,4-vinyl unit. Fractions of the vinyl unit and the inverted unit in trans-1,4 sequence which increased at high does rate inflected the change of dominant mechanism of polymerization.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3315-3317 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Topics: Chemistry and Pharmacology
    Notes: The synthesis and metal ion binding properties of a new class of functional oligomers are described. Oligo[1-(N-phenylthiocarbamoyl)aziridine] (DP ca. 8) and its analogs are prepared by ring-opening oligomerization of the corresponding aziridine monomers in good yields. These oligomers contain sulfur groups capable of binding “soft” metal ions, and the selective binding properties of the novel oligomer for Cu(II) and Hg(II) ions are investigated by liquid-solid adsorption and liquid-liquid extraction experiments.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3381-3391 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radiation-induced polymerization of isoprene in bulk state was studied at 25°C in a wide dose rate range. Variations of the rate of polymerization and molecular weight of the products were essentially the same as those observed in the monomers which were capable of both radical and cationic polymerizations. At low dose rate, 7.0-230 rad/sec, radical polymerization took place. At high dose rate, 8.8 × 103-2.2 × 105 rad/sec, radical and cationic polymerizations took place concurrently. The average molecular weight of the high-dose-rate product was about 850, independent of dose rate. The microstructure of the products at high dose rate consisted mainly of trans- 1,4 units with only about 7% of cis- 1,4 and 10% of 3,4-vinyl units. The residual unsaturation in the high-dose-rate products was 90%. Decreases in cis units and residual unsaturation at high dose rate were accounted for by the change in predominant mechanism of polymerization with dose rate.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3427-3439 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolymerization of butadiene with sodium styrene sulfonate was studied and the copolymer products characterized. In general these copolymers contain 0.5-4 mole% of sulfonated monomer. The effects of the following reaction variables are described: emulsifier type and concentration, monomers feed ratio, chain transfer agent concentration, and reaction conversion. The products were heterogeneous with regard to composition, molecular weight, and solubility behavior. Copolymers prepared under certain conditions exhibited strong intermolecular interactions derived from associations of the ionic species as observed in other ionomers.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3447-3454 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants and free energies of activation of Zn2+ -accelerated and Cr3+ -retarded condensations of resorcinolic A rings of polyflavonoid wattle tannins, as well as of the model compounds resorcinol and catechol with formaldehyde, were determined. A quantitative indication of the effect of strong metallic ion catalysts on phenol/aldehyde reactions was obtained. Second-order kinetics have been found to fit these metallic ion-catalyzed reactions. The dependence of the tannin/formaldehyde reaction on the concentration of Zn2+ and Cr3+ under acid and alkaline reaction conditions has been investigated and the respective catalytic coefficients determined. In the presence of the metallic ions used the reaction proved to be considerably less sensitive to variations of OH-concentration, hence of pH.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3483-3498 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Naphthalene-terminated polyvinyl aromatics and polyisoprene were obtained successfully. These functional polymers were metalated by potassium in THF at 25°C. The formation of a stable dinegative ion is observed unless the naphthalene is directly attached to the end of the polyvinyl aromatics, in which case a few isoprene units can be advantageously inserted between the naphthalene end group and the polyvinyl aromatics. The polymeric and stable dinegative ion polymerizes oxirane by both anionic sites and forms three-branched starshaped block copolymers.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1-8 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formation mechanism of an “asymmetric” porous structure for the film cast from ethyl acrylate-methyl methacrylate copolymer emulsion prepared by emulsifire-free emulsion polymerization was investigated. The formation of this structure was affected by the emulsion stability which was varied by the postaddition of sodium sulfate or sodium dodecyl benzene sulfonate. It is concluded that it is derived from the production of porous skin film at the emulsion-air interface and the precipitation of flocculated particles at the bottom of emulsion during drying process.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 51-55 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ultraviolet (UV) spectrophotometry was used to study the kinetics of basic hydrolysis of side groups in polyphenylmethacrylate in DMSO/H2O at various temperatures. Keller's mathematical analysis was applied to the description of the kinetics. Three rate constants which describe the reaction of ester groups with 0, 1, and 2 reacted neighboring groups, respectively, were determined. Activation energies for the hydrolysis reaction of the respective triads were calculated. The data confirmed the applicability of Keller's model to the computation of rate constants for the reaction of the respective triads in the polymer chain.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 27-34 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Block copolymers of styrene and 2-vinylpyridine of different molecular weights were synthesized and chemically modified to poly(vinyl pyridine)/poly(styrene sulfonate) or polystyrene/poly(2-vinyl pyridinium) salts. Adsorption on “Spherosil” silica with a high specific surface area was performed from aqueous solutions of polyelectrolyte copolymers or from noncharged copolymer in an organic medium and subsequent sulfonation or quaternization in the adsorbed state. The adsorption mechanism was studied under various solvent conditions to give silica maximal ion-exchange properties. Modification of silica resulted in a highly stable coated material which combines the mechanical properties of the porous beads and the ion-exchange properties of the “supported” and “pellicular” ion-exchangers and should have potential use in chromatography.
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  • 78
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 139-150 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polyurethane based on diphenyl methane diisocyanate (MDI) and propoxylated trimethylol propane was thermally degraded by using the techniques of pyrolysis and thermogravimetric analysis (TGA) in an inert atmosphere. Identification of pyrolysis gaseous products at 600°C showed that the first degradation step consists of a reversal of the polycondensation process, i.e., dissociation into starting polyol and diisocyanate, followed by the polyol degradation and a probable diisocyanate polymerization. Kinetic parameters were determined using dynamic and isothermal TGA curves. It is shown that the degradation can be closely compared with a random chain scission process.
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  • 79
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 165-174 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unit cell and probable space group of Nylon 5,7 has been determined. The unit cell is monoclinic with the dimensions a = 0.483 nm, b = 0.935 nm, c = 1.662 nm, and γ = 58.9°. The space group is probably Pb which is noncentrosymmetric. Rolled, annealed samples show three-dimensional orientation. The melting point peak of a rapidly cooled sample is about 213°C when it is heated at 20°C/min. Slow cooling, ≤°1°C/min generates a higher melting species, Tm = 228°C. Crystallinities are in the normal nylon range, up to 50% for a slow cooled sample.
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  • 80
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 151-164 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fully aromatic polyamide containing pyridine moieties (PPy) were successfully synthesized either by interfacial or solution polycondensation to prepare polyamide with inherent viscosity as high as 4. Solution properties of PPy in sulfuric acid were investigated in terms of solution viscosity and lyotropic behavior. The polyamide had a better solubility in sulfuric acid than in poly(p-phenylene terephthalamide) (PT) and the PPy solution in sulfuric acid exhibited an optically anisotropic property in a wider range of concentrations at relatively low temperatures in comparison with the PT solution. Viscosities of the PPy solution and the film cast from the PPy solution indicated a phenomenon characteristic of a highly oriented rigid polymer molecule caused by a lyotropic behavior.
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  • 81
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Gel formation usually occurs in crosslinking systems during polymerization. The critical conversion in this process is dependent on the reactivity ratios of the different kinds of double bond in the system and on the tendency to cyclization. In this article a procedure for estimating the gel point for small amounts of a symmetric divinyl compound is shown in measurements of the degree of polymerization at different conversions. A method is also given to relate the reactivity ratio of the pendent double bonds to the amount of cyclization and to the degree of multiple crosslinking. In m-divinylbenzene/styrene the results indicate that about 10% of the pendent double bonds is consumed by cyclization due to backbiting of the primary chain, whereas an initial effective crosslink results in about seven multiple crosslink bonds.
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  • 82
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 257-270 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of two-dimensional polymerization of octadecyl acrylate in lamellar crystal was investigated in two-step postpolymerizations by temperature increase and stepwiseγ-ray irradiation in lieu of the usual one-step reaction. Two-step postpolymerizations by these procedures are interpreted satisfactorily by the cone model, which assumes that the polymerization probability of the monomer molecules in a single layer is distributed conically around the initiation point. It was found that the propagating radicals were living, even in the saturated stage, and the effect of the polymer chains already formed on the propagating and terminating reactions was evident. Furthermore, molecular weight distributions of the resultant poly(octadecyl acrylate) measured by gel permeation chromatography (GPC) were broad. The values of Mw/Mn for the two-step post polymerizations were 4.71-7.03, whereas those for one-step reactions were 3.26-5.54.
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  • 83
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 295-304 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chlorination of poly(vinyl chloride) (PVC) was investigated by using deuterated polymeric models of PVC, viz., α-deuterated PVC (α-d-PVC) and β,β-dideuterated PVC (β,β-d2-PVC). The chlorinated samples of PVC, α-d-PVC, and β,β-d2-PVC were examined by combining infrared (IR), 1H-NMR, 13C-NMR, and mass spectroscopy. The results obtained were used in a study of the reaction mechanism of PVC chlorination. The selectivity of chlorination and the extent of the substitution and elimination-addition mechanism of chlorination are discussed with respect to the degree of chlorination and chlorination conditions.
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  • 84
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 371-380 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relative reactivity of acrylic acid is known to be influenced by the polymerization medium. Nonetheless, the more commonly used reactivity ratios do not show this dependence because they were calculated from low-conversion polymerizations. We have studied the copolymerization of acrylic acid and methyl methacrylate in a number of non-hydrogen-bonding and hydrogen-bonding solvents. We found that the acrylic acid fraction in the copolymer was larger when copolymerized in a non-hydrogen-bonding medium and that the methyl methacrylate fraction was larger when copolymerized in a hydrogen-bonding medium. The precise reactivity ratios were reported when toluene, benzene, isopentyl, acetate, ethyl acetate, methyl formate, and tert-butyl alcohol were used as the polymerization medium. The values were obtained by chromatographic analysis of residual monomer, followed by computation based on the nonlinear, least-squares technique of Tidwell and Mortimer.
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  • 85
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 397-402 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Red onion skin is highly effective for binding heavy metal ions from aqueous solutions. Color leaching can be prevented and the physical characteristics of the substrate can be improved by treatment with formaldehyde in an acidic medium. Batch and column experiments have been conducted with Cu2+, Cd2+, Zn2+, Ni2+, Hg2+, and Pb2+. Almost quantitative removal of the metal ions from solution can be achieved by using columns of the treated onion skin. Competition of the various metal ions for the substrate has been investigated. The capacity of the substrate in the majority of the metal ions studied is well above 1 meq/g. The use of polymerized onion skin to remove heavy metal ions from domestic and industrial wastewater to safe levels has been recommended as a cheap and effective alternative for commercial ion-exchange resins.
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  • 86
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 443-449 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The in-source polymerization of octadecyl acrylate in the lamellar crystal (hexagonal packing) by γ-ray irradiation has been investigated, as compared with the two-step and one-step postpolymerizations. The viscosity-average molecular weight is very high even in the initial stage and is practically saturated after 3-5 hr, although the conversion increases successively with time. The molecular weight distribution of poly(octadecyl acrylate) obtained by in-source polymerization is very wide (Mw/Mn = 13.1, at 20°C). The results of in-source polymerization of the long-chain vinyl compounds can be interpreted using the cone model for polymerization probability, similar to those of one-step and two-step postpolymerizations.
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  • 87
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 487-493 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aqueous polymerization of acrylonitrile initiated by the bromate - ferrous redox system in aqueous sulfuric acid was studied under nitrogen atmosphere. The rate of polymerization increased with increasing concentration of ferrous in the range of 0.25-1 × 10-2M. The percentage of conversion increased with increasing concentration of the catalyst, but beyond 2.5 × 10-3M there was a decreasing trend in the rate of polymerization. The rate varied linearly with [monomer]. The initial rate of polymerization as well as the maximum conversion increased within the range of 1-2.5 × 10-3M KBrO3, but beyond 2.5 × 10-3M the rate of polymerization decreased. The initial rate and limiting conversion increased with increasing polymerization temperature in the range 30-40°C; beyond 40°C they decreased. The effect of certain neutral salts, water-miscible solvents, complexing agents, and copper sulfate concentration on the rate of polymerization was investigated.
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  • 88
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 571-582 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of 1,3-cycloheptadiene (1,3-CHpD) with acrylonitrile (AN) in the presence of ZnCl2 leads spontaneously to the simultaneous formation of an alternating copolymer and a small amount of cycloadduct. The copolymer has a predominantly cis-1,4-structure. The formation of the charge - transfer complex between 1,3-CHpD and (AN)c (AN coordinated to ZnCl2) in AN was detected by ultraviolet (UV) spectroscopy. The activation energies for the cycloaddition and for the copolymerization under the conditions used were determined to be 17.6 (in the presence of 1,1-diphenyl-2-picrylhydrazyl) and 16.3 kcal/mole, respectively. The rate of copolymerization in AN was found to depend on the 1.5th power of the concentrations of (AN)c and of 1,3-CHpD. Oxygen and UV irradiation causes an acceleration of the copolymerization only. On the basis of these results the mechanism of the spontaneous copolymerization is discussed and its relation to the cycloaddition in systems of 1,3-cyclodienes and AN in the presence of ZnCl2 is mentioned.
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  • 89
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Polymerization of acrylonitrile and methyl methacrylate by the redox systems propanedinitrile-Mn(III) in aqueous sulfuric acid and propanedinitrile-Mn(OAc)3 in DMF and glacial acetic acid was investigated in the temperature range 20-40°C. The kinetics are consistent with the formation of an intermediate complex whose irreversible decomposition yields the initiating radical. With both monomers mutual termination predominates. The main difference between aqueous H2SO4 and acetic acid compared with DMF lies in the ease of oxidation of the primary radicals by the oxidant. Rate and equilibrium parameters were estimated and their significance discussed.
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  • 90
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Graft polymerization of acrylamide and sulfuric salt of 2-methyl-5 vinylpyridine onto cellulose using CO(III) salts was studied. It was shown that graft polymerisation of water-soluble polymers can be described by general relationships of radical reaction. The relation between elementary reaction constants of the formation and termination of active centers in cellulose, as well as relation between constants of the propagation, transfer and termination of chains were determined for different cellulose materials and monomers. The translational diffusion, sedimentation, viscosity, and flow birefringence of copolymers have been investigated in different solvents. Experimental data showed that the copolymers obtained are graft copolymers with two to five grafted chains onto macromolecules. The minimum distance between the branch points is 100 ± 20 glucoside units. The peculiarity of these copolymers is relatively low polydispersity. The conformation of macromolecules of such copolymers in solution depends on the compatibility of the copolymer components and the thermodynamic properties of the solvent.
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  • 91
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3403-3411 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several γ-alkoxy-β-hydroxypropyl acrylates were synthesized and polymerized. Both poly(MHPA) (IVd) and poly(MHPMA) (IVa) hydrogels possess high values of equilibrium water content, about seven and three times, respectively, that of the poly(β-hydroxyethyl methacrylate) hydrogel. These rather high values are attributed tentatively to the presence of a hydrophilic γ-methoxy-β-hydroxypropyl side group on the acrylic backbone.
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  • 92
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3413-3425 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Homopolymers of methyl α-fluoroacrylate (MFA), trifluoroethyl methacrylate (TFEM), and hexafluoroisopropyl methacrylate (HFIM) were prepared, as were their methyl methacrylate (MMA) copolymers. Copolymers of vinylidene fluoride (VDF) and chlorotrifluoroethylene (CTFE) with MMA were also prepared. The radiation susceptibilities of these polymers were measured by the 60Co γ-irradiation method, in which molecular weights were measured by membrane osmometry and gel permeation chromatography (GPC). All the copolymers degraded by predominant chain scission except poly(methyl α-fluoroacrylate), (PMFA), which crosslinks even at low doses (ca. 1 Mrad). The Gs - Gx and Gs values of the chain scissioning polymers and copolymers are higher than those of poly(methyl methacrylate) PMMA reference. The high susceptibility of PMFA homopolymer to crosslinking is in contrast to that of poly(methyl α-chloroacrylate), as we reported earlier. This effect is interpreted as resulting from extensive hydrogen fluoride and polyenlyl radical formation, which leads to facile crosslinking. However, incorporation of the MFA monomer unit causes the (22/78) MFA/MMA copolymer to degrade with a larger value of Gs that PMMA. Apparently a second-order process leads to crosslinking in PMFA and this is retarded in the copolymer. In the hehomopolymers of HFIM and TFEM and in the HFIM-MMA and TFEM-MMA copolymers the HFIM and TFEM components facilitate degradation with negligible crosslinking. The increased degradation susceptibility of VDF and CTFE copolymers with MMA over that of PMMA is attributed to processes at the VDF or CTFE components present in smaller concentrations (3-5 mole %) than the threshold levels (25-50% necessary for significant crosslinking).
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  • 93
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 327-333 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the γ-ray-initiated polymerization of acrylonitrile in bulk are reexamined in broad ranges of temperatures and radiation dose rates. The discussion of the results coupled with an analysis of earlier data indicate that the polymerization of acrylonitrile proceeds by different mechanisms depending on the reaction temperature. Above 60°C the precipitated growing chains recombine readily; therefore, the autoaccelerated conversion curves cannot be accounted for by an “occlusion effect.” It is suggested that autoacceleration is caused by a fast propagation taking place in oriented monomer aggregates which result from dipole-dipole association of the monomer with the polymer chains formed in the early stages of the reaction (“matrix effect”). Below 10°C the precipitated growing chains are buried in the dead polymer and monomer diffusion toward the occluded chain ends is very limited (“occlusion effect”). Between 10 and 60°C the system gradually changes from one dominated by “occlusion” to one where the “matrix effect” determines the kinetic behavior. The conclusion based on kinetic data is in agreement with results obtained from studies of the postpolymerization in these various systems.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 355-357 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 95
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 349-353 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 96
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1721-1732 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This investigation deals with the nature and relative abundance of stable radicals formed by gamma-irradiation of wheat starch at room temperature. Additions of equal weights of water, methanol, and ethanol were equally effective in reducing the content of stable radicals in starch which contained about 12% water before the additions. When, however, the starting material was dried starch with 2.9% initial water content additional water and methanol were better radical scavengers than ethanol. This difference is attributed to the superior ability of water and methanol to permeate the starch structure. Superficially different ESR spectra were obtained in products made by irradiating starch and starch that contained added water or methanol. Computer simulation of these spectra showed that they could be matched by superposition of the spectra of the same four component radicals, with some adjustments of relative intensities and peak widths. The structures of these radicals have been dedueed from the spectral assignments and relative effects of the three solvents used on the intensities of the respective ESR spectra.
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  • 97
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1037-1046 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New phenoxaphosphine-containing polyamide-imides were prepared by cyclodehydration of the polyamide-amic acids obtained from 8-chloroformyl-10-phenylphenoxaphosphine-2,3-dicarboxylic anhydride 10-oxide and diamines by a low-temperature solution polycondensation. Polymers with reduced viscosities of 0.10-0.59 dl/g in DMA or concentrated H2SO4 at 30°C were obtained in 64-97% yields. All the polyamide-imides were soluble in m-cresol, concentrated H2SO4, and dichloroacetic acid and some of them were soluble in DMF, DMA, and DMSO; the polyamide-imides had better solubility in organic solvents than phenoxaphosphine-containing polyimides. The phenoxaphosphine-containing polyamide-imides derived from aromatic diamines exhibited excellent thermal properties and little degradation below about 400°C, whereas the polymers from aliphatic diamines began to lose weight at about 250°C. They appeared to have thermal stability between phenoxaphosphine-containing polyimides and polyamides. These polyamide-imides exhibited self-extinguishing behavior.
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    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1085-1090 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The behavior of viologen polymer (P-V2+) as an electron transfer catalyst in the reaction of hydrogen generation was studied. In the photoirradiation system, which contains triethanolamine (TEA), Ru(bpy)3+3, and P-V2+, the amount of hydrogen evolution was less than methyl viologen (MV2+); P-V2+, however, was more effective in sodium dithionite as the electron donor and showed higher initial rates than MV2+.
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    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 380-380 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 100
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The plasma polymers prepared from perfluorocyclohexa-1,3-diene, perfluorocyclohexa-1,4-diene, and perfluorocyclohexene have been investigated by ESCA. The carbon-to-fluorine stoichiometries of the diene-derived polymers are similar and close to that of the starting material. The polymer prepared from perfluorocyclohexene is depleted in fluorine compared to the fluorine content of the “monomer.” The polymers prepared in nonglow regions are also studied and shown to be high in CF2 derived species. The results are compared with those for perfluorobenzene and perfluorocyclohexane, and the polymerization rates are in the order C6F6 〉 C6F8 1,3 ∼ 1,4 〉 C6F10 ∼ C6F12. The variations in composition of the plasma polymer as revealed by ESCA as a function of the polymerization conditions are discussed.
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