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  • Physics  (7,053)
  • 42.55
  • Calcium
  • Volumetrie
  • Wiley-Blackwell  (7,054)
  • Springer  (348)
  • Essen : Verl. Glückauf
  • Krefeld : Geologischer Dienst Nordhein-Westfalen
  • 2015-2019
  • 2005-2009
  • 1980-1984  (2,877)
  • 1970-1974  (2,660)
  • 1965-1969  (1,865)
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  • 1
    Electronic Resource
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    Springer
    Applied physics 33 (1984), S. 115-131 
    ISSN: 1432-0649
    Keywords: 02.20 ; 42.55 ; 42.60D
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This study puts forward the concept of helical distributed feedback (DFB) lasers. The basic features of this new type of laser are derived by group theoretical considerations on cylindrical, circular linear periodic, and helical waveguide and laser structures. It is demonstrated that not only linear periodic structures but also helical structures show Bragg and DFB effects. Microwave and far-infrared experiments on passive helical metal waveguides reveal Bragg resonances in transmission. These results initiated the first experimental realization of a helical DFB gas laser, i.e. an optically pumped 496μm CH3F laser with a helical metal waveguide of a pitch close to 250μm. This helical DFB laser shows higher-mode selectivity than the corresponding linear DFB laser. Finally, we show that the concept of helical DFB also applies to dye lasers with internal DFB incorporated by a mixture of the dye with a cholesteric liquid crystal.
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  • 2
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    Applied physics 34 (1984), S. 17-21 
    ISSN: 1432-0649
    Keywords: 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Twenty-four new optically pumped submillimetre laser lines have been observed when CH3OH is excited using a13C18O2 pump laser. Four of these lines have been assigned to transitions involving the CO stretching band. In addition to these lines, a further six new lines have been observed when pumping with12C18O2 and13C16O2 lasers. One of these lines has been assigned to a transition involving the CO stretching band. The observation of infrared-infrared double resonance signals in CH3OH has allowed the prediction of a further six laser lines which should be excited using a13C18O2 pump laser.
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  • 3
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    Applied physics 34 (1984), S. 221-228 
    ISSN: 1432-0649
    Keywords: 42.55 ; 41
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The conditions under which a cooperative emission from different friges occurs in the scattering between a relativistic electron beam and two interfering laser beams are discussed. In particular, the conditions to have an electron grating are discussed.
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  • 4
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    Applied physics 35 (1984), S. 77-82 
    ISSN: 1432-0649
    Keywords: 42.55 ; 42.65
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The coexistence of bistability and repetitive passive Q-switching of a CO2 laser with a gaseous saturable absorber has been investigated experimentally. With CH3F as the saturable absorber bistability has been observed simultaneously with passive Q-switching, whereas with CH3OH either one of these phenomena can only exist, as demonstrated for the first time. The measured features of both systems can be explained qualitatively by rate-equation theory.
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  • 5
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    Applied physics 35 (1984), S. 127-129 
    ISSN: 1432-0649
    Keywords: 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Strong submillimetre laser action has been obtained on five lines of a new laser gas, formaldoxime. Several new emission lines have also been produced by isotopic CO2 laser pumping of14NH3 and15NH3. One of these lines at 102.9 μm is a rotation-inversion transition in the 2v 2 state, and is the first example of cw laser action in such a highly excited state.
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  • 6
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    Applied physics 33 (1984), S. 23-27 
    ISSN: 1432-0649
    Keywords: 42.55 ; 42.60
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract For the first time stable cw output of a FIR-CO2 hybrid laser has been achieved at wavelengths shorter than 300 μm. Due to the saturable absorber characteristic of the FIR laser gas, cw or pulsed emission is observed on both, the CO2 and the FIR laser output, depending on the operating conditions. Results are reported on different resonant lines in CH3OH and the 67 μm Raman line in NH3. The good efficiency of this laser is also demonstrated by the excitation of two new emission lines in CH3OH, namely 49 and 56 μm, pumped by 9R(22) and 9R(24), respectively.
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  • 7
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    Applied physics 34 (1984), S. 83-86 
    ISSN: 1432-0649
    Keywords: 33.50 ; 34.50 ; 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract An XeF pumped vapor phase POPOP dye laser with a pulse duration of 300 ns was obtained when trans-stilbene was used as triplet quencher. An energy conversion efficiency of 7,5% with a peak power efficiency of 12% was measured.
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  • 8
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    Applied physics 34 (1984), S. 175-177 
    ISSN: 1432-0649
    Keywords: 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract 47 new cw far-infrared laser lines with wavelenths between 453 and 2356 μm have been obtained by optically pumping vinyl bromide (C2H3Br) by a CO2 laser. A significant portion of these lines has wavelengths longer than 750 μm.
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  • 9
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    Applied physics 35 (1984), S. 163-166 
    ISSN: 1432-0649
    Keywords: 42.50 ; 42.55 ; 42.60
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We present an analytical expression for the small-signal gain of a Free Electron Laser (FEL) in the presence of a Gaussian mode. To describe the electron beam evolution we use the one-dimensional (1-d) Vlasov equation. Our perturbation result, valid for small values of the parameterq (length of the undulatorL divided by the Rayleigh rangeZ R), can be extrapolated to values ofq≈4÷5.
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  • 10
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    Applied physics 33 (1984), S. 9-16 
    ISSN: 1432-0649
    Keywords: 42.60 ; 42.20 ; 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We derive the most general equations of motion for the electrons and the electromagnetic field in a free-electron laser including the effects of diffraction and pulse propagation. The field evolution is expressed in terms of the amplitudes and phases of a complete set of transverse modes. The analytic solution is given in the small-signal regime, where the theory is shown to be in excellent agreement with a recent experiment at Orsay.
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  • 11
    ISSN: 1432-0649
    Keywords: 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Experiments on pressure dependence of a CF4 laser have been carried out to elucidate dynamic characteristics of CF4 molecules pumped by CO2 lasers. The results are followed by a model calculation which characterizes collisional quenching of the energy levels related to the stimulated emission. The enhancement of the laser output induced by buffer-gas addition, which was found under specific conditions, is discussed in relation to the competition between laser and superfluorescent emissions.
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  • 12
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    Applied physics 33 (1984), S. 235-238 
    ISSN: 1432-0649
    Keywords: 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract An intensive generation of radiation from a discharge-pumped atomic-fluorine gas laser is reported. A peak power exceeding 330 kW and a total energy of more than 2 mJ is obtained for a number of lines in the red, using a NF3∶He (1∶100) gas mixture at total pressure of 500 Torr. The circuitry optimization is described and the conditions for effective operation of the atomic-fluorine laser are discussed. The temporal and the spectral characteristics of the laser emission are also presented.
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  • 13
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    Applied physics 35 (1984), S. 71-75 
    ISSN: 1432-0649
    Keywords: 42.60 ; 42.55 ; 42.72
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A simple model of the energy transfer between a booster dye and the active dye in a flashlamp pumped planar waveguide dye laser is described. Analytical results are compared with experiments for several dyes in the 600–650 nm region. A twofold increase of laser output was found at a wavelength (630 nm) which is of particular interest for several applications.
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  • 14
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    Applied physics 33 (1984), S. 187-193 
    ISSN: 1432-0649
    Keywords: 42.50 ; 42.55 ; 42.60
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract It is shown by numerical analysis based on Lamb's equations of motion, that standing-wave lasers with purely homogeneously broadened emission lines exhibit regular multimode oscillations. Specifically, modes lying far from the line centre are quenched due to mode competition, and the amplitudes of the oscillating modes approach steady-state values. The stabilization of the amplitudes is normally accompanied, or followed, by an evolution of the phases towards a phase-locked regime, where the relative phasesψ n = 2φ n −φ n + 1 −φ n − 1 [φ n phase in then th mode, defined by (6)] attain either the value 0 or ± π. The build-up times for the relative phases are found to vary over a wide range.
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  • 15
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    Applied physics 35 (1984), S. 11-15 
    ISSN: 1432-0649
    Keywords: 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The temporal development of the small-signal gain on the Cl2(D′−A′) transition at 258 nm has been investigated by means of an amplified spontaneous emission (ASE) technique. For electron beam pumped He/Cl2 mixtures, the gain appears only at the end of the pumping pulse, whereas for He/Cl2/CCl4 mixtures the temporal gain profile coincides with the fluorescence pulse, and the maximum gain coefficient increases by about a factor of two. The observed effects are due to the mixing of both halogen donors and can be explained by considering the quenching of theD′-state by electrons.
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  • 16
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    Applied physics 34 (1984), S. 191-192 
    ISSN: 1432-0649
    Keywords: 42.55 ; 42.60
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A pulsed xenon ion laser has been used to pump a rhodamine 6G dye laser utilizing a ring resonator. The dye laser has been passively mode-locked; a pulsewidth of 0.5 ps and a 50 kW peak power have been obtained.
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  • 17
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    Applied physics 35 (1984), S. 227-231 
    ISSN: 1432-0649
    Keywords: 42.55 ; 42.60
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The feasibility of using the electrically excited XeF(C»A) excimer medium as an efficient wideband amplifier in the blue-green region of the spectrum has been investigated. Calculations show that for an intense blue-green optical flux input the amplification characteristics of XeF(C»A) improve, as a result of both bleaching of the pump induced absorbers and by additional production of XeF(C) level population. The removal of one of the major absorbing species, Xe** in the XeF (C»A) laser mixture by means of a pulsed ruby laser probe beam has been demonstrated.
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  • 18
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    Calcified tissue international 36 (1984), S. 139-144 
    ISSN: 1432-0827
    Keywords: 1,25(OH)2-vitamin D ; Weight loss ; Phosphate ; Calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary During a review of 42 metabolic studies in healthy women and men we observed that serum 1,25-(OH)2-D concentrations were directly correlated to the observed daily changes in body weight (r=0.68;P〈0.001) and to caloric intake/kg/day (r=0.39;P=0.01). These relationships could not be accounted for by related and physiologically expected changes in serum Ca or iPTH concentrations. However, serum 1,25-(OH)2-D concentrations were observed to be inversely correlated to serum PO4 levels (r=−0.44;P=0.004). In addition, serum PO4 levels were inversely correlated to the daily changes in body weight (r=−0.40;P=0.009). Since dietary sodium intake averaged 142 mmol/day, it is unlikely that the observed changes in weight were the result of changes in salt and water balance. Thus it seems reasonable to speculate that serum 1,25-(OH)2-D concentrations may vary directly with energy balance, as reflected by changes in body weight. This effect may be mediated by alterations in PO4 metabolism. The accurate assessment of serum 1,25-(OH)2-D levels thus appears to require several measurements over time periods during which body weight is stable.
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  • 19
    ISSN: 1432-0827
    Keywords: Electromagnetic field ; Bicarbonate ; Phosphate ; Calcium ; Fluoride ; Osteogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The present studies are aimed at establishing molecular correlations in the interaction of very low frequency electromagnetic fields with biological systems. Ca-uptake by chick embryo tibia rudiment in short-term culture was a useful model. Tibiae of 8- to 10-day-old chick embryos were incubated 60 min in simplified culture media in the presence of45Ca at 37.5±0.5°C either inside or outside pulsating electromagnetic fields. Radioactivity count in the medium was the most accurate method for determining Ca-uptake by the rudiment. The effect of the fields on the Ca-uptake depended markedly on the chemical composition of the culture medium: bicarbonate was indispensable; glucose or sucrose was important; phosphate was potentiating; ethanol, Mg2+, and NaF were stimulating. The field had no effect in (a) blank medium without tibia, (b) tibiae that had been altered by fixation with aqueous glutaraldehyde, (c) nonliving artificial systems endowed with great or small ion sorption capacity. The unique bicarbonate effect with living systems and the passive behavior of nonliving ion sorbing systems prompt the suggestion that the electromagnetic field probably couples with specific processes, such as a bicarbonate-dependent Ca2+ ATPase and the active ion transport, at the cell membrane level. The molecular mechanisms remain to be established.
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  • 20
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    Calcified tissue international 36 (1984), S. 194-199 
    ISSN: 1432-0827
    Keywords: Benzo(B)Thiophene-2-Carboxylic Acid ; Bone cells ; Calcium ; Cyclic AMP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The purpose of the present study was to investigate the mechanism of action on bone of Benzo(B)Thiophene-2-Carboxylic Acid (BL-5583). BL-5583, at a dose range of 0.01–100 µg/ml, inhibited spontaneous as well as A23187 and PTH-induced bone resorption in tissue culture. This compound also decreased calcium uptake in both osteoclastic and osteoblastic enriched bone cell populations obtained by sequential collagenase digestion of 1–2 day newborn rat calvariae. The decrease occurred after a 5 min. incubation with45Ca and BL-5583. The effective dose range was 0.01–100 µg/ml. No effect on leucine incorporation or lactic acid production by bone cells was observed. BL-5583 also induced a transient decrease in calcium uptake in skin cells isolated from fetal rats by collagenase digestion, suggesting a lack of tissue specificity for this compound. No effect on cyclic AMP in isolated bone cells was observed with the same dose range that produced a calcium effect.
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  • 21
    ISSN: 1432-0649
    Keywords: 33.80 Bx ; 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract In this work, clear FIR Raman emission in ammonia was observed when a 9P20 CO2 line was used as a pump. We have noted an intense pump depletion and strong superradiant FIR and MIR emissions. The time history of these radiations has also been recorded. The intense MIR radiation is a new line observed in the ammonia laser.
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  • 22
    ISSN: 1432-0649
    Keywords: 42.60 ; 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract To improve the gain in the Orsay storage ring Free Electron Laser (FEL) experiment, the 17 period permanent magnet undulator has been modified to form an optical klystron (OK). We report the measurement of spontaneous emission and the effects on it of energy spread and angular spread. Gain and laser induced bunch lengthening measurements with the OK are also reported and are in very good agreement with the FEL classical theory. The spontaneous emission spectrum which is easy to measure with good signal to noise ratio, turns out to be a very good diagnostic tool forenergy spread and angular spread measurements on storage rings. The factor of four increase in the small gain obtained by converting the undulator NOEL into an OK was the critical factor in the recent operation of the ACO storage ring laser above threshold.
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  • 23
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    Applied physics 35 (1984), S. 167-172 
    ISSN: 1432-0649
    Keywords: 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Fluorescence at 490 nm from the triatomic excimer Xe2Cl* has been investigated to determine the 308 nm absorption due to this species in an x-ray preionized, self-sustained gas discharge XeCl laser. The dependence of Xe2Cl* density on laser intensity (at 308 nm), buffer gas and Xe and HCl partial pressures has been determined for discharges with a peak electrical power deposition of 2.5 GWl−1. Xe2Cl* absorption is estimated to reach 0.6% cm−1 under non-lasing conditions but decreases to a non-saturable 0.2% cm−1 for intracavity laser intensity〉1 MW cm−2. XeCl* and Xe2Cl* fluorescence intensities were found to be a similar for both helium and neon buffer gases but laser output was a factor of two greater with a neon buffer.
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  • 24
    ISSN: 1432-0827
    Keywords: Calcium ; Vitamin D deficiency ; 1,25(OH)2D3 ; Parathyroidectomy ; Parathyroid hormone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Studies presented here were designed to investigate further the basis for an impaired cAMP response to parathyroid hormone (PTH) in osteoblastlike calvarial bone cells isolated from vitamin D-deficient rat pups. The goal was to perturb Ca, PTH, and vitamin Din vivo in order to see which factors might be responsible for the impairedin vitro bone cell cAMP response. Pups either were parathyroidectomized (PTX) 3–5 days, implanted with osmotic minipumps delivering high doses of PTH, given repeated, high doses of 1,25(OH)2D3, or were D-deficient (-D, i.e., born and suckled by D-deficient mothers). Osteoblastlike bone cells, isolated by sequential enzyme digestion and centrifugation, were exposed to PTH for 5 min in the presence of a phosphodiesterase inhibitor. In bone cells isolated from -D rat pups, both basal and PTH-induced cAMP accumulation were significantly lower than in +D bone cells. Earlier, we had shown that two daily injections of -D pups with 50 ng 1,25(OH)2D3 restores this reduced bone cAMP response of -D pups toward normal. In the present study, neither basal nor PTH-induced bone cell cAMP accumulation was affected by subjecting D-replete pups to PTX, PTH infusion, or repeated high doses of 1,25(OH)2D3 despite the fact that each treatment markedly changed serum Ca or serum immunoreactive PTH. The results indicate that the impaired bone cell cAMP response seen in -D pups is not a direct result of chronic hypocalcemia and that the “heterologous desensitization” seenin vitro with added 1,25(OH)2D3 could not be duplicated byin vivo treatment of +D pups with supraphysiologic doses of 1,25(OH)2D3. Finally the lack of alteration in the bone cell cAMP response to PTHin vitro after chronic PTH infusionin vivo fails to support the notion that the impaired response in -D bone cells can be explained entirely by “homologous desensitization” induced by high circulating levels of PTH in the hypocalcemic, -D rat pup.
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  • 25
    ISSN: 1432-0827
    Keywords: Calcitonin ; Parathyroid hormone ; Calcium ; Newborn ; Fracture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Determinations of serum calcium (Ca), phosphorus (P), calcitonin (CT), and parathyroid hormone (PTH) were carried out in 36 full-term newborn infants with fracture of the clavicle (CF) and in 46 normal neonates (N). At the 6th hour of life the CF neonates demonstrated lower serum Ca and higher serum CT in comparison with normal infants. In the hours following, no significant differences between the two groups for the Ca levels were found, whereas serum CT remained significantly higher in the CF newborns at the 24th, 48th, and 72nd hour of life. Significant differences between normal and CF infants in the PTH serum levels were detected only at the 48th hour, when PTH was lower in the CF newborns. The results of this investigation indicate that the fracture of the clavicle is a significant and peculiar factor in stimulating CT secretion. Serum Ca level appeared to be controlled by CT rather than auto-regulating the secretion of the hormone.
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  • 26
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    Calcified tissue international 36 (1984), S. 596-603 
    ISSN: 1432-0827
    Keywords: Calcium ; Ameloblasts ; X-ray microanalysis ; Transport ; Frozen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Energy dispersive X-ray microanalysis was applied to freeze-dried blocks of enamel organ tissue to determine levels of calcium in various celular regions. The tissue blocks were dissected free from adjacent forming enamel following injection of cobalt or fluoride ions, both of which temporarily inhibit enamel mineralization. In all control and experimental specimens there was an increasing gradient of calcium from the stratum intermedium cells to the distal ends of the ameloblasts. Calcium levels were significantly reduced near the distal ends of the ameloblasts following cobalt or fluoride injection as compared with controls. It is suggested that evidence of an intercellular buildup of calcium near the distal ends of the ameloblast supports a controlling function of these cells. The changes in calcium levels are correlated with alterations in mineralization known to occur in the adjacent enamel of the model systems employed.
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  • 27
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    Calcified tissue international 36 (1984), S. 77-82 
    ISSN: 1432-0827
    Keywords: Osteogenesis ; Diffusion chambers ; Alkaline phosphatase ; Calcium ; Phosphorus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The alkaline phosphatase activity and the calcium and phosphorus content of osteogenic tissue formedin vivo following the implantation of diffusion chambers loaded with rabbit bone marrow cells is reported. (In this study the term osteogenic includes osteoblastic and chondroblastic.) Chambers examined 14–70 days after implantation revealed progressive accumulation of mineral. Alkaline phosphatase activity increased until day 30 and declined thereafter. The osteogenic potential of the marrow cells decreased with increasing weight (age) of the cell donor rabbit when measured either as the percentage of chambers containing osteogenic tissue or as the amount of calcium, phosphorus, or alkaline phosphatase activity within the chambers. The results confirm that measurements of these parameters in tissue formed by cells incubated in diffusion chambersin vivo may be used as a method for assay of osteogenesis.
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  • 28
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    Calcified tissue international 36 (1984), S. 269-273 
    ISSN: 1432-0827
    Keywords: Bone loss (osteopenia) ; Calcium ; Corticosteroids (glucocorticosteroids) ; Fluoride ; Vitamin D
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary To evaluate the effect of prednisone and triple treatment (sodium fluoride, calcium, and vitamin D) on trabecular and cortical bone serial bone mineral content (BMC) measurements were made at a metaphyseal (BMCD) and diaphyseal (BMCP) site on the forearm on 31 consecutive and previously bone-healthy patients scheduled for at least 24 weeks high-dose prednisone treatment. The patients were randomized into two further treatment groups: group I (n=16) received prednisone plus triple treatment and group II (n=15) received only prednisone. The two groups were similar with regard to age, sex, prednisone dose, and initial BMC. During 24 weeks treatment, BMCD (partially representing trabecular bone) and BMCP (mainly representing cortical bone) fell significantly and similarly, demonstrating that there is no preventive effect on bone mineral loss on the triple regimen. The BMC fall after 12 weeks was significantly more pronounced for metaphyseal (partially trabecular) than for diaphyseal (cortical) bone, whereas the values did not differ significantly after 24 weeks; this indicates a greater sensitivity to the hormone treatment of trabecular bone. In the entire group, the fall in BMC correlated positively with individual prednisone dose, significant at the diaphyseal site (r=0.39,P〈0.05), but not at the metaphyseal site (r=0.31, P=0.08). It is concluded that corticosteroid-induced osteopenia is a diffuse bone disease which affects trabecular as well as cortical bone, suggesting that BMC measured on the forearm reflects changes in bone mineral at other locations.
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  • 29
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    Calcified tissue international 36 (1984), S. 392-400 
    ISSN: 1432-0827
    Keywords: Vitamin D ; Chick embryo ; Bone ; Calcium ; Phosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Chick embryos were injected in the yolk sac at various ages with various doses of different vitamin D3 metabolites. Serum concentrations of total calcium and inorganic phosphate were determined 24 h after the injection and histological and electron microscopic studies of the tibiae were conducted 3–6 days after. Confirming previous results, the injection of 1,25(OH)2D3 was found to produce significant hypercalcemia and hypophosphatemia. The dose required to produce these effects decreased with age: 100 ng on the 9th day, 50 ng on the 11th, and 10 ng on the 15th. This finding is interpreted as resulting from the fact that the specialized cells in the chorionic epithelium which are considered to be involved in mineral resorption from the shell differentiate between the 11th and 13th days. Although no bone changes were observed in embryos injected before the 11th day, a rim of unmineralized trabeculae (osteoid) was observed at the periphery of the cortex of the tibial diaphysis in the embryos which had been injected after that age. Thus, in embryos injected on the 11th day with 100 ng 1,25(OH)2D3, the trabeculae formed between the 11th and 14th day remained unmineralized until the 15th or 16th day at which time they completed their mineralization. In the embryos injected on the 14th day, the alterations were more severe and could be produced with doses 10 times smaller than those required when the injections were made on the 11th day. At all ages, the doses that produced an osteoid rim also induced hypercalcemia and hypophosphatemia. The electron microscopical study of the osteoid trabeculae showed that osteoblasts and osteocytes had normal cytological characteristics and that the bone matrix did not present changes other than the reduction in mineral deposition. While the above findings do not exclude a direct action of 1,25(OH)2D3 on bone cells as the mechanism of osteoid formation, they do underline the importance of the humoral changes at least as partial determinants of this phenomenon. The activities of various vitamin D metabolites were compared using as parameter the threshold-dose required to produce a rim of unmineralized trabeculae in the tibia of 14–15 days embryos (T-D). The most active metabolite appeared to be 1,25(OH)2D3 (T-D: 10 ng); it was followed by 1,24,25(OH)3D3 (T-D: 100 ng) and 1,25,26(OH)3D3 (T-D: 100 ng). Vitamin D3 itself (T-D: 100 µg), 25(OH)D3 (T-D: 2.5µg) and 24,25(OH)2D3 (T-D: 5 µg) produced similar responses but only when administered in much larger doses.
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    Calcified tissue international 36 (1984), S. 702-710 
    ISSN: 1432-0827
    Keywords: Corticosteroids ; Cartilage ; Organ culture ; Calcium ; Matrix vesicles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The present study examined the effects of various corticosteroid and noncorticosteroid hormones upon the ultrastructure of chondroprogenitor cells and chondroblasts in an organ-culture system of late fetal condylar cartilage. Corticosteroids, (triamcinolone acetonide, dexamethasone, corticosterone) at concentrations of 10−6–10−8M stimulated markedly a precocious formation of matrix vesicles by chondroblasts. This stimulation was accompanied by a significant accretion of calcium complexes intra- and extracellularly in both the chondroprogenitor cell population and chondroblastsin vitro, as well as in the newly induced matrix vesicles. Nonglucocorticoid steroids (progesterone, estradiol, testosterone, cortexolone) did not evoke similar effects. Progesterone and testosterone, however, seemed to adversely affect the ultrastructure of the cartilage cells, whereas estradiol appeared to have a favorable effect on the morphology of cultured condylar cartilage.
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  • 31
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    Archives of microbiology 138 (1984), S. 140-152 
    ISSN: 1432-072X
    Keywords: Caulobacter ; Prostheca development ; Stalk function ; Calcium ; Phosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Calcium was found to stimulate stalk development in Caulobacter crescentus and to relieve the inhibition of development long known to be caused by phosphate. This suggested that phosphate inhibition could be attributed to its interaction with Ca2+, thereby depriving the cells of a factor that promoted development. Calcium was also found to promote phosphate acquisition by the cells, observed as acceleration of growth at extremes of phosphate concentration, as promotion of carbon-source utilization rather than storage, and as support for phosphate-dependent resistance to arsenate inhibition of growth. Cytological studies of dividing cells revealed that stalked siblings had greater access to exogenous phosphate for use in growth or for storage as polyphosphate, and that access of non-stalked sibling to phosphate was dependent on the length of the stalk of the dividing cell. It was concluded that the physiologic role of the stalk is enhancement of phosphate acquisition. The stimulatory role of calcium in this process was attributed to its support of stalk development and to its stabilization of internal membrane/cell envelope association within the cell-stalk juncture.
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  • 32
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    Archives of microbiology 139 (1984), S. 102-104 
    ISSN: 1432-072X
    Keywords: Fungus ; Zoospore ; Blastocladiella ; Allomyces ; Gamma ; Particle ; Phosphate ; Calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The elemental composition of gamma particles in zoospores ofAllomyces macrogynus andBlastocladiella emersonii was determined by use of energy dispersive X-ray analysis of glutaraldehyde fixed, thin section zoospores. Isolated preparations of gamma particles were also examined. Gamma particles contained no detectable elements. Similar sized, globular, electron dense cytoplasmic inclusions contained phosphorus and calcium. We suggest that previous studies assigning calcium and phosphorus to gamma particles may have been based on confusion of these two types of cytoplasmic inclusions.
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  • 33
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    Planta 160 (1984), S. 12-20 
    ISSN: 1432-2048
    Keywords: Calcium ; Calmodulin ; Germination (spore) ; Onoclea ; Phytochrome and Ca2+ ; Pteridophyta
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Phytochrome is confirmed to be the photoreceptor pigment in the germination response of Onoclea sensibilis L. by demonstrating red-far-red (R-FR) photoreversibility. External Ca2+ is required for this response with a threshold at a submicromolar concentration. Ethylene glycol-bis(β-amino-ethyl ether)-N,N,N′,N′-tetraacetic acid, La3+ and Co2+ reversibly inhibit germination. Lanthanum only inhibits germination when applied before or during irradiation, indicating that the external Ca2+ requirement is transient, although in the absence of Ca2+ the R-stimulated system remains maximally poised to accept the ion for over 4 h after irradiation. The ability to respond to Ca2+ 4.1 h after R-irradiation is not reversed by FR-irradiation, indicating that Ca2+ transport has been uncoupled from phytochrome. Barium and Sr2+, but not Mg2+ can substitute for Ca2+. Artificially increasing the concentration of intracellular free Ca2+ with the ionophore A 23187 stimulates germination in the dark. The Ca2+-calmodulin antagonists, trifluoperizine and chlorpromazine, reversibly inhibit germination. Calcium is required in phytochrome-mediated fern spore germination; it may be acting as a second messenger.
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  • 34
    ISSN: 1432-0878
    Keywords: Ionophore A-23187 ; Calcium ; Exocrine pancreas ; Secretion ; Zymogen granule
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Rat-pancreas lobules were incubated with the ionophore A-23187 in the presence of Ca2+. After 90 min, some of the acini were partially or almost completely depleted of their zymogen granules while others had the appearance of resting acini. With few exceptions, the cells of a given acinus were degranulated to a comparable level. Slight dispersion of the zymogen granules was noticed in cells incubated in a Ca2+-free medium containing EGTA with or without A-23187. In the presence of Ca2+ the secretory response obtained with the ionophore was comparable to that observed with 10-5M urecholine. The results obtained provide cytological evidence that the secretory response is only partially determined at the membrane-receptor level and that other mechanisms intervene between cytosol Ca2+ increase and exocytosis.
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  • 35
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    Cell & tissue research 236 (1984), S. 237-244 
    ISSN: 1432-0878
    Keywords: Aster formation ; Calcium ; Endoplasmic reticulum ; Hypertonic stress ; Parthenogenetic stimulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Sea urchin eggs exposed to a continuous hypertonic treatment rapidly form many concentric whorls of endoplasmic reticulum (ER) during the pre-activation period of the parthenogenetic development. These whorls, however, are only a temporary configurational alteration of ER which begin to break up just prior to egg activation. The conversion back to normal vesicles and lamellae occurs not only concurrently with the appearance of early cytastral areas, but also frequently in close association with the formation of these membranous areas. It is revealed here that membrane elements from disrupting whorls may become incorporated into adjacent, developing clear areas, early cytastral areas, and that this ER constitutes an initial major source of membranes for these early astral areas. Having previously suggested that the actual formation of ER whorls occurs in direct response to released intracellular calcium in hypertonic stressed eggs, the new findings, along with other related data and correlations, further suggest that whorl disruption and the formation of associated astral areas can be correlated with a corresponding decrease in the concentration of this released calcium in the cytoplasm.
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    Protoplasma 120 (1984), S. 209-215 
    ISSN: 1615-6102
    Keywords: Fusion ; Calcium ; Protoplast ; Membrane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Rather than selecting for a chemical fusogen one can select for a fusogenic plant membrane (i.e., one that will fuse readily). Wild carrot suspension culture cells can be grown under conditions which cause the released protoplasts to have a high potential to fuse. Protoplast fusion is enhanced by calcium and inhibited by EGTA. When 10mM calcium (pH6.0) is added, fusion percentages of 60% are common. The mild fusion treatment appears to have no effect on callus regeneration and differentiation.
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  • 37
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    Protoplasma 121 (1984), S. 17-24 
    ISSN: 1615-6102
    Keywords: Chilling-sensitivity ; Calcium ; Chlortetracyline ; A 23187 ; Lycopersicon ; Digitalis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary We have investigated the possibility that the rapid low temperature effects upon cyclosis and subcelluar structure might be due to a breakdown in compartmentation of intracellular calcium, leading to an increase in cytoplasmic Ca2+. Changes in fluorescence of chlortetracycline (CTC), a probe for membrane-bound Ca2+ were monitored in the corners of individual trichome cells (effective spot size ca. 800 square microns) with the aid of a Zeiss epifluorescence microscope linked to a Zeiss Zonax analyzing system. A consistent decrease in signal was observed as cells of chilling-sensitiveLycopersicon esculentum Mill. (cv.Ace) were cooled below their threshold temperature for chilling sensitivity. On rewarming, as the temperature rose above the chilling threshold, there was an increase in fluorescent signal. In contrast, trichomes ofDigitalis purpurea (chilling-resistant) showed no such changes. The uncoupling agent, CCCP, and the Ca2+-chelator, EGTA, induced marked decreases in the fluorescent signal in cells from both species. A more direct approach to testing the hypothesis was to examine the effect of modulating cytoplasmic Ca2+ with the aid of the Ca2+ -ionophore A 23187 and a Ca2+ concentration series in EGTA buffer. Above 10−8 M external free Ca2+, streaming began to be inhibited, full inhibition occurring at 5 x 10−6M Ca2+. The strand structure started to disappear when the Ca2+ rose above 10−7M. Disappearance of strands was accompanied by an increase in the number of cells with vesiculated cytoplasm, an effect analogous to that of chilling temperatures on these cells. The phenothiazines, trifluoperazine and chlorpromazine (10−5M) had similar effects. However but such effects were not seen with R 24571 or N(6-aminohexyl)5-chloro-1-napthalenesulfonamide (W 7) until concentrations were reached that orders of magnitude above their IC50 for calmodulin.
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  • 38
    ISSN: 1615-6102
    Keywords: Calcium ; Contraction ; Discophrya ; Ionophore A23187 ; Ruthenium red ; Tentacles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The tentacles of the suctorian protozoonDiscophrya collini are stimulated to contract by externally applied Ca2+. The role of extracellular Ca2+ in tentacle contraction was studied by monitoring45Ca2+ uptake, using ionophore A23187 to facilitate membrane transport of calcium and ruthenium red (RR) as an inhibitor of transport. The degree of tentacle retraction was dependent upon external Ca2+ concentration and studies with45Ca2+ using scintillation counting indicated a linear relationship between external Ca2+ concentration and Ca2+ uptake. Uptake of Ca2+ was enhanced in the presence of the ionophore while RR caused little inhibition.45Ca2+ uptake was only partially inhibited by RR when cells were subjected to a Ca2+, ionophore and RR mixture. Grain counts from light microscope autoradiographs after treatment of cells with45Ca2+/ionophore,45Ca2+/RR or45Ca2+ alone showed heavy, light and intermediate labelling respectively. In all instances the grains were evenly distributed within the cell. These observations are interpreted as supporting the suggestion that the ionophore enhances both the uptake of extracellular Ca2+ and release of Ca2+from an internal source, while the RR could only partially prevent movement of Ca2+ through the plasma mebrane. A model is presented suggesting that tentacle retraction is mediated by cytosolic Ca2+ levels which are determined by the fluxing of Ca2+ across the plasma membrane and the membrane of elongate dense bodies which act as internal Ca2+ reservoirs.
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  • 39
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    Plant and soil 76 (1984), S. 319-337 
    ISSN: 1573-5036
    Keywords: Aggregates ; Aluminium ; Bacterial mucilage ; Binding agents ; Calcium ; Cation bridges ; Complexing agents ; Dispersion ; Electron microscopy ; Electrophoretic mobility ; Fungal hyphae ; Glues Iron ; Management Periodate ; Polysaccharides ; Rhizosphere ; Roots ; Slaking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The stability of pores and particles is essential for optimum growth of plants. Two categories of aggregates macro- (〉 250 μm) and micro- (〈250 μm) depend on organic matter for stability against disruptive forces caused by rapid wetting. Dispersion of clay particles from microaggregates is promoted by adsorption of complexing organic acids which increase the negative charge on clays. The acids are produced by plants, bacteria and fungi. However, the dispersibility of clay in microaggregates is offset by the binding action of polysaccharides, mainly mucilages produced by bacteria, but also by plant roots and fungal hyphae. The stability of microaggregates is also enhanced by multivalent cations which act as bridges between organic colloids and clays. Macroaggregates are enmeshed by plant roots, both living and decomposing, and are thus sensitive to management, and increase in number when grasses are grown and the soil is not disturbed. Lack of root growth,i.e. fallow, has the opposite effect. Various implications for management of soil structure are discussed.
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    Plant and soil 78 (1984), S. 367-379 
    ISSN: 1573-5036
    Keywords: Acidity ; Aluminium ; Calcium ; Manganese ; Nodulation ; pH Rhizobium ; Rhizosphere ; Root elongation ; Root hairs ; Trifolium repens ; White clover
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Effects of factors associated with soil acidity (low pH, low calcium, high aluminium and high manganese) on theTrifolium repens-Rhizobium trifolii symbiosis were investigted under laboratory conditions using an axenic solution-culture technique. 200 μM manganese increased root elongation in the range pH 4.3–5.5, but had no effect on root hair formation, the number of Rhizobium in the rhizosphere, or nodule formation. Root elongation and root hair formation were unaffected at pH 4.3 when 500 or 1000μM calcium was supplied, whereas multiplication of Rhizobium in the rhizosphere and nodulation were inhibited at pH 4.3 and 4.7.50–1000μM calcium had no effect either on the multiplication of Rhizobium in the range pH 4.3–5.5, or on nodule formation in the absence of aluminium. 50 μM aluminium inhibited, root elongation and root hair formation at pH 4.3 and 4.7; the effect on root elongation was reduced by increasing the calcium concentration from 50 to 1000μM. 50μM aluminium also inhibited Rhizobium multiplication in the rhizosphere and reduced nodule formation at pH 5.5 (at which aluminium precipitated out of solution), but root elongation and root hair formation were unaffected. These, effects of aluminium at pH 5.5 may explain the poor response to inoculation by white clover in acid mineral soils after liming.
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  • 41
    ISSN: 1573-5036
    Keywords: Calcium ; Cation de liaison ; Complexes organo-minéraux ; Minéralisation ; Stabilisation de la matière organique ; Structure ; Calcium ; Cation bridge ; Fixation of organic matter ; Mineralisation ; Organomineral compounds ; Structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Description / Table of Contents: Summary By gradually removing the exchangeable calcium held by the organo-mineral complex of an organic soil from the Jura mountains, the authors showed: a direct action of the microflora on the mineralisation of organic matter (Fig. 7) and on the generation of mineral nitrogen (Fig. 3); an indirect action by the mineralisation of organic matter on the destabilisation of the clay-humus complex. They therefore concluded that the reduction of calcium resulted in the destabilisation of the organo-mineral complex by H+, produced by the biodegradation of the most labile portion of the organic matter. The clay humus complex gradually dissociated. This process lead to the destruction of aggregates and organo-mineral complexes. The organic matter released became biodegradable due to the shortage of calcium.
    Notes: Résumé Les auteurs sont partis d'un complexe organo-minéral calcique provenant d'un sol humifère du Jura et ont provoqué une diminution progressive au cours du temps du taux de calcium échangeable. L'étude de l'évolution de divers paramètres, menée parallèlement, a permis d'analyser les effets directs et indirects de la baisse du calcium sur le complexe organo-minéral. Les résultats obtenus concernent: 1. les effets directs de l'action minéralisatrice de la microflore sur la dégradation de la matière organique (Fig. 7) et la production d'azote minéral (Fig. 3). 2. les effets indirects de cette minéralisation sur la déstabilisation du complexe argilo-humique (Fig. 8). Ils permettent d'affirmer qu'un complexe organo-minéral calcique évolue très rapidement quand l'apport d'ions calcium vient à diminuer ou à être supprimé. Les ions Ca2+ sont très vite déplacés et remplacés par des ions H+ produits par la biodégradation des fractions les plus labiles de la matière organique. Le complexe argile-calcium-humus est progressivement dissocié. Le processus conduit à une destruction des agrégats avec libération des argiles et de la matière organique qui devient à son tour biodégradable. l'effet stabilisateur du calcium ayant disparu.
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  • 42
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    Plant and soil 79 (1984), S. 101-121 
    ISSN: 1573-5036
    Keywords: Base saturation ; Bio-climatic zones ; Calcium ; Clay accumulation ; Copper ; C:N ratio ; EDTA ; Forest soils ; Greece ; Iron ; Magnesium ; Manganese ; Nitrogen ; Phosphate ; Potassium ; Soil classification ; Zinc
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Soils derived from a number of different parent materials (lithologies) and developed along a climatic gradient, manifested by the altitudinal succession of natural vegetation zones (Mediterranean, sub-Mediterranean, Mountainous and Pseudoalpine), were sampled throughout mainland Greece. In soils derived from siliceous parent materials low in clay, acidity increase and percent base saturation decreases from the Mediterranean to the Pseudoalpine vegetation zones. Clay illuviation is found mainly in soils developed in the Mediterranean and the sub-Mediterranean zones. No such changes are apparent in clayey soils rich in bases. Organic matter content of the mineral portion of the soil profile increases by a factor of 2 with a decrease in mean annual air temperature of about 10°C. The pattern of change in clay and soil organic matter content with climate is in relatively good agreement with soil development trends in the area, when soil profiles are named according to the FAO-Unesco soil map of the world. Concentrations of Ca and Mg decrease and those of total N, total and extractable P, K, Fe, Mn and Zn increase from the Mediterranean to the Mountainous zone. Within the same zone, however, concentrations of N, Ca, K, Fe, Mn and Zn decrease, but those of Mg, total and extractable P increase with soil depth. The concentrations of most macro- and micronutrients in the humic horizon are several times higher than those in the mineral portion of the soil profile due to biological enrichment.
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  • 43
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    Plant and soil 82 (1984), S. 61-67 
    ISSN: 1573-5036
    Keywords: Calcium ; Glomus caledonium ; Glomus mosseae ; Lactuca sativa ; Vesicular-arbuscular mycorrhiza
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Infection of lettuce roots (Lactuca sativa L.) by the vesicular-arbuscular mycorrhizal fungiGlomus caledonium andGlomus mosseae was dependent on the amount of calcium (supplied as CaCl2·2H2O or CaSO4·2H2O) in the nutrient solution; those plants growing at low calcium concentrations being poorly infected.
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  • 44
    ISSN: 1573-5036
    Keywords: Aluminium toxicity ; Calcium ; Phosphate ; Trifolium ; Uptake ; Nutrients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Hydroponic experiments were undertaken to examine the effect of increasing aluminium levels on the mineral nutrition and root morphology ofT. repens growing in nutrient solution. Toxicity symptoms appear between 27.8 and 47.5 μM Al3+ activity (148 to 297 μM total aluminium). The threshold level corresponding to a 10% reduction in leaf fresh weight is estimated to be approximately 20 μM Al3+ activity. The concentration of aluminium in the leaves of white clover increases exponentially with aluminium activity in the nutrient solution. The uptake of divalent cations was inhibited but aluminium enhanced potassium and nitrogen concentrations in both leaves and roots. At high pH (pH 6.0) the speciation of aluminium is controlled by the formation of solid aluminium phosphate and aluminium hydroxide except at the lowest aluminium level (37 μM) where 99.9 per cent is present as the DTPA complex. As the concentration of total aluminium increases, the percentage of Al-DTPA and soluble aluminium hydroxide decreases whilst solid Al(OH)3 increases rapidly to reach a maximum of 91.6 percent (of the total aluminium) in the 1180 μM aluminium treatment. At pH 4.5 the dominant forms of aluminium are free aluminium ion Al-DTPA, AlSO 4 + and AlOH2+. The roots of aluminium stressed plants showed symptoms typical of aluminium toxicity.
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  • 45
    ISSN: 1573-5036
    Keywords: Calcium ; Eucalyptus saligna ; Eucalyptus wandoo ; Foliar nutrients ; Magnesium ; Nitrogen ; Phosphorus ; Potassium ; Rehabilitation ; Seasonal trends
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Seasonal changes in the foliar concentration of macronutrients (N, P, K, Ca and Mg) in sapling trees ofEucalyptus saligna Sm. andE. wandoo Blakely growing in rehabilitated bauxite mined areas in the Darling Range of Western Australia are described. Foliar N concentration decreased with age of the fully expanded leaf tissue. Leaf N concentrations were also high when rates of litter decomposition were expected to be high during the period of early spring. The greatest foliar N difference between trees growing in good soil conditions and those from poorer soil conditions also occurred during this period. Levels of P in leaves were highest in young developing leaves but once the leaves reached full size, no seasonal trend in P concentration was observed. Foliar K was lower during the winter and probably related to the period of maximum leaching by precipitation. High foliar K during summer, however, could be related to the role of K in lowering cellular water potential. Leaf Ca was highest during early sping. Low mobility of cellular Ca during the cool portion of the year was indicated. Foliar Mg showed a weak pattern of decreasing concentration with leaf age. The best season for sampling for these broadleafed evergreen species to provide information on plant nutrient status appears to be in spring.
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  • 46
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    Plant and soil 80 (1984), S. 181-190 
    ISSN: 1573-5036
    Keywords: Adsorption ; Calcium ; CEC ; Cell wall ; Clover ; Exchange ; Magnesium ; Model ; Potassium ; pH ; Root ; Rye-grass
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The ion exchange properties of clover and rye-grass root cell walls were studied quantitatively. Three sets of experiments were performed: adsorption of Ca, Mg and K ions versus pH, adsorption versus cation concentration and exchange isotherms Ca−Mg and Mg−K. A model has been developed. It allows the satisfactory prediction of results (except for pH curves) with the adjustment of a minimum of parameters. The total charge (RT), on its own, accounts for the difference between the ion exchange properties of the clover and rye grass cell walls. The selectivities observed on root material are very different from those observed on soil exchange complexes. The decreasing affinities of cell walls for cations follow the sequence: Ca〉Mg≫K for cell walls. These differences of selectivity are much larger than those usually observed for soil exchange complexes.
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  • 47
    ISSN: 1573-5036
    Keywords: Branch nutrients ; Calcium ; Eucalyptus saligna ; Eucalyptus wandoo ; Foliar nutrients ; Magnesium ; Nitrogen ; Phosphorus ; Potassium ; Rehabilitation ; Soil nutrients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The macronutrient variation within four 6 year oldEucalyptus saligna and four 5 year oldE. wandoo growing on rehabilitated bauxite pits was determined. Significant differences in mean nutrient concentrations were generally recorded between good soil condition sites and poor soil sites, between tree individuals, branch height, and plant organ type; but mean nutrient values were not different among canopy aspects. Fully expanded leaves of the current year provided the most uniform nutrient levels among the plant organs and showed major differences between sites with good soil nutrient conditions and those with poor conditions. Differences in foliar and branch levels of N, P, K, Ca and Mg, the variation between sites, canopy heights and plant organ types, and the use of foliar nutrient levels to indicate deficiencies are discussed.
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  • 48
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1065-1076 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Various phosphorus-containing polyimides were prepared by the reaction of 1-[(dialkoxyphosphinyl)methyl]-2,4- and -2,6-diaminobenzenes (1) with a tetracarboxylic dianhydride like pyromellitic dianhydride (PMDA) and benzophenone tetracarboxylic dianhydride (BTDA). In addition, copolyimides that contained approximately 3% phosphorus were prepared by the reaction of 1 and m-phenylenediamine (MPD) with the aforementioned tetracarboxylic dianhydrides. Elemental analysis, inherent viscosity, infrared (IR) spectroscopy, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) studies were performed to characterize the polymers. Their thermal properties were compared with those of the corresponding common polyimides. It was shown that the molecular weight and thermal stability of the polymers were reduced as the concentration of the phosphorus moieties increased. The fire-resistance of the copolyimides was evaluated by determining their limiting oxygen index (LOI) value. Copolyimides that contained about 3% phosphorus showed an LOI value approximately 30% higher, than the value of the corresponding common polyimides. In addition, a model diamic acid and diimide was synthesized by the reaction of 1-[di(2-chloroethoxyphosphinyl)methyl]-2,4- and - 2,6-diaminobenzene (DCEPD) with phthalic anhydride and characterized by elemental analysis, IR, proton nuclear magnetic (1H-NMR) spectroscopy, DSC, and TGA. The pyrolysis behavior of the model compounds was investigated by gas chromatography-mass spectrometry (GC-MS). A direct cleavage of the P—C bond and a possible rearrangement to diisocyanates occurred during their pyrolysis.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1123-1130 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thin film coatings were prepared by polymerizing trifluoromethyl-substituted aromatic compounds in a glow discharge with low power levels and medium pressures. Smooth, continuous films which are adherent and insoluble in conventional solvents were produced. A significant amount of the fluorine content from the monomer was retained in the polymer. The trifluoromethyl group was not removed by the plasma conditions and appeared in the film as trifluoromethyl and difluoromethylene groups. The films were slightly less wettable than those of the unfluorinated films.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1153-1177 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Asymmetric polyamides from the reaction of either optically active trans-1,2-cyclopropanedicarboxylic acid (C3) or trans-1,2-cyclohexanedicarboxylic acid (C6) with 2,7-diazaspiro[4,4]nonane(DSN) were synthesized. The possible conformations of these polymers and their model compounds in 2,2,2-trifluoroethanol (TFE), water, methanesulfonic acid (MSA), and sulfuric acid were examined by circular dichroism (CD), NMR, viscosity, and dipole moment measurements. The racemic polyamides (±)C3·(±)DSN and (±)C6·(±)DSN exist in extended forms. No intrinsic viscosity changes were observed for these two polymers in TFE and MSA. Certain viscosity and spectral changes have been observed for the optically active polyamides, although no specific ordered conformations can be assigned. The optically active diacid units incorporated into the polymer give a conformation unique from the totally extended chain. CD studies seem to evidence some conformational differences among the polyamide derived from (+)C6 diacid and the optically active DSN. By changing the solvent from TFE to MSA a blue shift of the trough was observed for (+)C6·(±)DSN, a red shift for (+)C6·(-)DSN, and an inversion of the CD spectrum for (+)C6·(+)DSN polyamides. The results of the work with (+)C6·(-)DSN in dilute acid solution suggest that the rotation around the C-N bond is a relatively low-energy process. The spectral and intrinsic viscosity data are consistent with this suggestion. No drastic spectral changes have been observed for the C3·DSN polyamides by changing the solvent from TFE to MSA. The amide group in the C3·DSN polyamide and the corresponding model compound prefer a similar conformation with the carbonyl group bisecting the cyclopropane ring. The C3·DSN polyamide seems to exist in an extended form.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1515-1524 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cationic grafting of polystyrene initiated by carbon black containing the CO+ClO-4 group was investigated. The introduction of CO+ClO-4 groups onto a carbon black surface was achieved by the reaction of AgClO4 with carbon black that contained a COCI group. The latter was introduced by the reaction of carboxyl groups with SOCl2. It was found that polystyrene chains could be grown from CO+ClO-4 groups on the surface of carbon black. Moreover, polystyrene was effectively grafted from carbon black: the grafting ratio at 20°C increased to 58% as conversion increased. Furthermore, the grafting ratio and molecular weight of ungrafted polystyrene decreased with an increase in polymerization temperature. These results were explained by the fact that the increasing temperature of the polymerization caused an increase in the rate of chain transfer reaction of the growing polymer chain to the monomer. The carbon black obtained from the reaction produced a stable colloidal dispersion in a good solvent for polystyrene.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1541-1550 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical polymerization of several alkyl allyl oxalates, including methyl allyl oxalate (MAO), ethyl allyl oxalate, propyl allyl oxalate, butyl allyl oxalate, and octyl allyl oxalate, was conducted in the evolution of carbon dioxide at elevated temperatures, and was compared with the anomalous polymerization behavior of diallyl oxalate (DAO) discussed in our earlier articleA. Matsumoto, I. Tamura, M. Yamawaki, and M. Oiwa, J. Polym. Sci. Polym. Chem. Ed., 17, 1419 (1979).. The kinetic equations for the polymerization of alkyl allyl oxalate were derived following the kinetic treatment of the DAO polymerization by further consideration of the absence of cyclization of the growing polymer radical and the effective reinitiation by alkyl radical, and were then satisfactorily applied to the polymerization of MAO, as a representative alkyl allyl oxalate. The evolution of carbon dioxide in the polymerization of alkyl allyl oxalates was enhanced with the increase of bulkiness of the alkyl substituent, as a result of steric suppression of the propagation of the growing polymer radical.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 17-28 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Plasma polymers synthesized by inductively coupled RF techniques have been investigated as a function of operating parameters for the isomeric perfluorinated diazines (pyrazine, pyrimidine, and pyridazine). A combination of ESCA and microanalytical studies shows that plasma polymers are produced by rearrangement mechanisms: the C/F and C/N stoichiometric ratios are similar to those of the starting monomers over a range of operating parameters. A comparison of rates of formation of plasma polymer films reveals distinctive differences between the isomeric diazines that suggest that equilibration of valence isomers occurs on a substantially slower time scale than for isomeric fluorinated benzenes5-9 which, in general, polymerize at essentially the same rates. In contrast to the remarkably low critical surface tension of plasma polymers based on perfluorobenzenes (ca. 20 dynes cm-2), the plasma polymer films from the perfluorinated diazines which are initially hydrophobic become hydrophilic in contact with water droplets. This is attributed to the hydrolytic instability of films associated with the labilizing influence of nitrogen on nucleophilic displacement of fluoride which is a feature of the chemistry of monomers.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 49-60 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies were conducted on grafting of acrylamide (AM) and sodium-2-acrylamido-2-methylpropane sulfonate (NaAMPS) comonomers onto dextran utilizing Ce(IV) induced initiation. The effects of reaction temperature, the Ce(IV)/dextran ratio, and the AM/NaAMPS ratio on grafting yield were investigated. The graft copolymerization behavior can be explained by exchange of the AMPS anion with one of the ligands on the Ce(IV) initiator. Oxidative modification of the dextran substrate improved the yield of graft copolymer. The dextran-g-poly(acrylamido-co-sodium-2-acrylamido-2-methylpropane sulfonate) samples prepared by this method were characterized as to copolymer composition and molecular weight utilizing elemental analysis, dilute solution viscometry, and aqueous size exclusion chromatography. Relationships of molecular weight and charge density to kinematic viscosity and salt sensitivity are discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 77-84 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoinitiated cationic polymerization by photosensitization of diphenyliodonium and triphenylsulfonium salts is shown to proceed by two distinct electron transfer process: (1) direct electron transfer from excited-state photosensitizers and (2) indirect electron transfer from photogenerated radicals. The efficiency of the former process is attributed to the instability of the reduction products (from diphenyliodonium and triphenylsulfonium salts), which dissociate in competition with undergoing energy-wastage reverse electron transfer. Amplification of photons in the production of protons (or other reactive cations) is postulated to account for the high quantum yields observed in the latter process. Potential advantages of utilizing the indirect redox process in the design of UV curable hybrid systems, which contain functionality for both radical and cationic polymerization, are noted. The results also provide evidence against the importance of triplet states of the onium salts in photoinitiator activity.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 107-120 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Racemic and optically active N-carboxyanhydrides (NCA)s of 2-methyl- and cis-6-methylpipecolic acid, when subjected to polymerization conditions in solution or in bulk whether with “weak” or “strong” base initiators, resisted polymerization under all conditions tried. Instead, the NCA of 2-methylpipecolic acid gave the corresponding cyclic dipeptide and the NCA of cis-6-methylpipecolic acid formed the cyclic dipeptide derived from trans-6-methylpipecolic acid. The mechanism of dimerization of these NCA's was investigated. Evidence was provided for the proposed mechanism in which the active moiety is not a carbamate ion but an amino group. Methyl 2-methylpipecolate underwent an intermolecular SN2-type reaction upon heating, yielding equimolar quantities of methyl N-methyl-2-methylpipecolate and 2-methylpipecolic acid.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 135-144 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of a range of 10 organic nitriles on the radiation-induced polymerization of styrene was studied. A dose rate of 4.4 rad s-1 was used. A rate of polymerization of styrene (1.744 mol L-1 of toluene solution) of 5.0 × 10-7 mol L-1 s-1 was found. With organic nitriles present (styrene:nitrile ratio of 1:0.28) the rate of polymerization increased. Rates in the range of 5.5 × 10-7 -5.2 × 10-6 mol L-1 s-1, depending on the nitrile present, were obtained. The polymers were partially characterized and evidence of involvement of each of the nitriles in the polymer chains was revealed. The increase in rate of polymerization has been attributed to the part played by nitrile radicals in the initiation of styrene polymerization. Radical yield values [as G(nitrile radical)] were derived from the relevant rate expressions. Values ranged from 2.7 to 49.5, depending on the particular nitrile. Corresponding values of G(nitrile radical) in the range of 5.1-129.4 were obtained by the manipulation of number-average molar mass data. Values of kpkt of approximately 2 × 10-5 L mol-1 s-1 were found. Trommsdorff types of effect are absent from these systems.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 213-223 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: The effect of parasubstituents on the radiation chemistry of poly(α-methylstyrene) (PMS) was compared for the fluoro (PFMS), chloro (PCMS), bromo (PBMS), isopropyl (PiPMS), and methoxy (PMeOM) derivatives. Radiolysis yields, ESR spectra, and GC—MS analysis of products were obtained. PMS and PFMS have similar low radiolysis yields, products, and product distributions. Only main-chain radicals which persist to 200° were observed. PCMS has increased values of Gs, Gx, and Gr. The product analysis results suggest that the presence of chlorine contributes to the primary process by dissociative electron capture and enhances the cleavage of α-methyl group. Irradiation of PBMS caused crosslinking and yielded few volatile products. PMeOMS and PiPMS gel readily by γ-irradiation and may be useful as negative radiation resists.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 225-238 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: High molecular weight polysilane copolymers which contain the units in the title were prepared in high yield by sodium coupling the corresponding organodichlorosilanes in toluene. These copolymers are highly soluble in common solvents and can be drawn into fibers or formed into films by molding or casting. They are also photoactive.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 277-281 
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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 22 (1984), S. 303-318 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Iron-ion-containing polymers were prepared by reacting atactic polyvinylpyridine with ferric chloride or ferric nitrate in methanol solution. Molar ratios of Fe3+ to 4-vinylpyridine (Fe:PVP) were 1:2, 1:6, and 1:20. Three kinds of iron center were characterized from 57Fe Mössbauer spectra recorded over a temperature range of 4.2-290 K. Infrared (IR) spectra of the samples were measured also. All samples contained amorphous hydrated ferric-oxide particles that exhibited superparamagnetic behavior at low temperatures. The size of the clusters (102-103 iron atoms per particle) was estimated from the average blocking temperatures TBav, which is sensitive to the Fe:PVP ratio. For FeCl3:PVP preparations with Fe:PVP of 1:2, 1:6, and 1:20 TBav was 37, 10, and 〈4 K, respectively. A small proportion (〈10%) of high-spin ferrous iron centers was found in most samples. A third type of signal attributable to oxygen-bridged ferric dimers was found in FeCl3-PVP preparations with Fe:PVP of 1:2 or 1:6 but not in Fe(No3)3-PVP samples. This species is probably [Cl3Fe—O—FeCl3]2-. Interactions between the polymer and the various iron centers were weak.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 341-352 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Five general routes for the preparation of polyoxyethylene [generally referred to as poly(ethylene glycol) or PEG] derivatives are described. These routes are (1) nucleophilic displacements with the alkoxide of PEG, (2) nucleophilic displacement on PEG-tosylate, -mesylate, or -bromide, (3) reductive amination of PEG-aldehyde, (4) reductive amination of PEG-amine, and (5) nucleophilic displacements on the s-triazine derivatives prepared from s-triazine trichloride (cyanuric chloride) and PEG. Eighteen derivatives are prepared and potential applications to catalysis, cell purifications, and other areas are discussed briefly.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 391-406 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: The polymerization of 6-amino-2,4-trans,trans-hexadienoic acid and various of its salts was studied in the solid state. Crystals of the hydrochloride and organic inorganic double halides with cadmium chloride, manganese (II) chloride, and iron(II) chloride were found to polymerize rapidly upon UV or γ irradiation. An erythro-diisotactic polymer is obtained in the form of extended chain crystals. The polymer behaves as an amphoteric polyelectrolyte. The kinetics and the mechanism of the polymerization as well as morphological changes during the solid state reaction are discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 419-428 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: ESCA and contact-angle (H2O and CH2I2) measurements are used to follow changes in the surface of poly(ethylene terephthalate) film photooxidized (254 nm radiation in O2) for varying times, followed by aging for as many as three weeks or washing with water. Photooxidation occurs uniformly throughout the outermost 50 Å of the film to give a surface stoichiometry that corresponds to C10O6.6. Oxidation produces mainly carboxyl (acid) and alcohol/phenol groups, carbonyls form after extensive treatment. Low molecular weight products formed by chain scission and oxidation are removed by washing and diffuse into the bulk when aged. Oxidized products in higher molecular weight chains are not removed by washing, but can diffuse into the polymer bulk or reorient because of their chain mobility; therefore they are directed toward the polymer bulk rather than the surface. Extended photooxidation produces a stable oxidized surface more resistant to aging changes. The results are compared with those obtained for poly(ethylene terephthalate) film oxidized in an electrical discharge.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 463-473 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: The absolute rate constants of propagation (kp) and of termination (kt) of N-acryloylpiperidine (NAPi) were determined by the rotating sector method in bulk; kp = 273 and kt = 1.79 × 107 L/mol s at 30°C. It was noted that kp for NAPi was 100 times smaller than that for N,N-dimethylacrylamide (DMAcAm). The absolute rate constants of cross-propagations for copolymerizations with common monomers were evaluated by combination of the kp value and the monomer reactivity ratios. Quantitative comparison of the rate constants with those of DMAcAm and poly(DMAcAm) radical shows that NAPi is as reactive as DMAcAm and the smaller kp value for NAPi is ascribable to much the lower reactivity of the poly(NAPi) radical. The large difference in reactivity of the polymer radicals is discussed in relation to the steric factor of the piperadino and the dimethylamino groups which seems to affect the capability of the carboxamide group to stabilize the polymer radical.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 493-502 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preirradiation grafting of N-vinylpyrrolidone (NVP) onto poly(tetrafluoroethylene) (PTFE) and poly(tetrafluoroethylene-hexafluoropropylene) (FEP) films was investigated. The influence of grafting parameters such as preirradiation dose, monomer concentration, and grafting temperature on the rate and grafting yield was studied. Different solvents were used for diluting the monomer and it was found that the aqueous monomer solution at a concentration of 80 wt% was suitable for this grafting system. However, the graft polymerization of NVP in benzene terminated within a short time without significant grafting yield. The dependence of the grafting rate on preirradiation dose and monomer concentration was 1.2 and 1.07 order, respectively, for grafting onto PTFE films and 1.1 and 1.2 order, respectively, for grafting onto FEP films. Arrhenius plots for grafting onto PTFE films showed a breaking point at ca. 35°C and the overall activation energies were calculated as 23.6 and 9.0 Kcal/mol below and above 35°C, respectively. For grafting onto FEP films, however, no break was observed in the Arrhenius plots; the overall activation energy was 11.9 Kcal/mol. The swelling behavior and electric resistance of the grafted materials were investigated.
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  • 67
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    Notes: Several polythioesters by interfacial polycondensation of 1,4-di(mercaptomethyl)-2,3,5,6-tetramethylbenzene with oxalyl, succinyl, adipoyl, suberoyl, and sebacoyl chlorides were obtained. To determine the optimal conditions for interfacial polycondensation, the influence of the following factors on yield and value of reduced viscosity were studied: type of organic phase, concentration of hydrogen chloride acceptor, the quantitative ratio of aqueous to organic phase, molar ratio of reagents; temperature of reaction, rate of acid chloride addition, and contribution of catalyst. Thorough studies were carried out only for polycondensation of the dithiol with adipoyl and sebacoyl chlorides. The structure of all polythioesters obtained under the model conditions was determined by elementary analysis and infrared spectra. Initial decomposition temperature, mass loss in percentage at the same temperature, maximum rate of decomposition, and mass loss percentage at 100-400°C were defined by thermogravimetric analyses. Chemical resistance of the polythioesters was determined by treatment with some organic solvents, mineral acids (concentrated and 10%), and sodium hydroxide (10 and 50%). Some mechanical and electrical properties of the polythioesters obtained from dithiol and adipoyl and sebacoyl chlorides were determined. The molecular weight was not measured because of the low solubility of the polythioesters.
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    Notes: The anionic polymerization of norbornene trisulfide initiated with sodium thiophenoxide (sodium cation solvated with dibenzo-18-crown-6 ether) was studied. Polymers with high molecular weights were obtained (Mn up to 105, osmometrically). Molecular weights calculated for living polymerization conditions (i.e., one molecule of initiator yields one macromolecule) agree well with Mn measured by osmometry. 1H-NMR, 13C-{1H}-NMR, and Raman spectra of the polymer are given. Thermodynamics of polymerization in toluene solvent is described. Enthalpy ΔHss = -(1.39 ± 0.17) kcal mol-1 and entropy ΔSss = -(7.52 ± 0.55) cal mol-1 deg-1 coefficients of polymerization were evaluated from the temperature dependence of the equilibrium monomer concentration determined dilatometrically.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1141-1151 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A fire- and heat-resistant polymer was obtained by the thermal polymerization of bismaleimido-substituted 2,2-bis(anilino)-4,4,6,6-tetrakis-(4-Aminophenoxy)-cyclotriphosphazene. The thermal stabilities of the polymer were evaluated in nitrogen and in air by thermogravimetric analysis. This polymer was stable to 345°C and had char yields of 78% at 800°C in nitrogen and of 71% at 700°C in air. The structures of cyclotriphosphazene precursors and the polymer were characterized using Fourier-transform infrared and proton nuclear magnetic resonance spectroscopy.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1187-1190 
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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 22 (1984), S. 1197-1200 
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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 22 (1984), S. 1243-1250 
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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 reaction of alkyl halides with aqueous sodium acetate or cyanide catalyzed by phosphonium salts supported on insoluble polystyrene resins, and rates of ion-exchange of the chloride ion in the catalysts against the acetate ion, were studied as a function of catalyst particle size, the percentage of ring substitution, the morphology of polymer support, and distance between active site and polymer backbone. Rates of 1-bromooctane or benzyl chloride with macroporous, 7-25% ring-substituted catalysts increased with increasing ring substitution. Rates with macroporous catalysts increased as a heptamethylene spacer was introduced between the active site and the polymer backbone. Rates of ion-exchange with macroporous catalysts were facilitated with increasing ring substitution or by the introduction of the spacer chain. A relation between the catalytic activity of macroporous or microporous catalysts and ion-exchange rates under triphase conditions was discussed.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1251-1258 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Polymerization of the cyclic amide of PIII is described for the first time. The N,N-diethylamine-1,3,2-dioxaphosphorinan was shown to give living reversible polymerization with anionic initiators. Lithium and sodium derivatives were found to be inactive. 1H-, 13C-, and 31P-NMR indicated that the polymer strictly reflects the monomer structure and is formed without any isomerization, the polymer chain being $\rlap{--} ({\rm OP}\left( {{\rm NR}_{\rm 2} } \right){\rm O(CH}_{\rm 2} \rlap{--} )_3 )_n $. Initiation involves attack of the anion on the P atom. From the dependence of the equilibrium monomer concentration on temeprature ΔH1s = 1.5 ± 0.2 kcal·mol-1 and ΔS1s = 4.6 ± 0.6 cal·mol-1·°K-1.
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    Topics: Chemistry and Pharmacology
    Notes: The interaction of α-poly-L-lysine and ε-poly-L-lysine with methyl and ethyl orange was studied by equilibrium dialysis and spectroscopic methods. The results of the dialysis measurements indicated that the extent of binding by ε-polypeptide is substantially higher than that by α-polypeptide, despite the much greater molecular weight of the latter. This difference in binding affinity was interpreted in terms of the increased conformational adaptability of ε-polypeptide because of its highly flexible structure. Furthermore, ε-polypeptide exhibited strong cooperative binding. In addition, the effect of the successive addition of α- and ε-polypeptides on the absorption spectra of methyl and ethyl orange was investigated. The addition of α-polypeptide with a molecular weight of 400,000 produced a new absorption peak at a shorter wavelength, due to the stacked dye molecules on the polypeptide chain, whereas that of ε-polypeptide did not. From the results of spectroscopic measurements a possible mode of interaction between these two polypeptides and the small molecule is discussed.
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  • 75
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1327-1333 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Grafted PMMA was isolated by the acid hydrolysis method. Weight-average and number-average molecular weights were determined by gel permeation chromatography. The number-average molecular weight of the grafted chains was about 475,000 for amylopectin and 403,000 for amylose. The number of grafted chains (mmol) ranged from 2.4 × 10-3 to 4.6 × 10-3 for amylopectin graft copolymers and from 2.9 × 10-3 to 6.8 × 10-3 for those of amylose. These results were related to others obtained from ceric ion consumption studies. The values suggest that amylopectin, because of its complex structure, favors a higher consumption of ceric ion in homopolymerization reactions and inhibits the initiation reactions of the copolymerization.
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  • 76
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1365-1372 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The progressive dissolution of carboxylated latex particles with increasing pH was utilized to investigate the internal structure of core-shell latex particles, in comparison with that of copolymeric latex particles formed from the same monomers. The results indicated that in those latex particles which are formed when ethyl acrylate (EA) -methacrylic acid (MAA) or methyl acrylate (MA) -MAA mixture is polymerized in the presence of poly(MA-MAA) or poly(EA-MAA) seeds the shell is composed of the more hydrophilic poly(MA-MAA) molecules relatively high in MAA content and the core is composed of both poly(MA-MAA) and poly(EA-MAA) molecules, regardless of the order of the stage feed, while the copolymeric latex particles are relatively uniform from surface to center in distribution of all components except MAA. Examination of the distribution of the carboxylic groups in all of the latex particles showed their concentration to be highest at the surface and to decrease with proximity to the center in accordance with other findings reported in the literature.
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  • 77
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1409-1417 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The emulsion polymerization of styrene initiated by potassium persulfate catalyzed by Ti+3 ions was studied. Two sources of Ti+3 ions were used: the titanium trichloride and titanium sulfate. It was found that the titanium ions used in conjunction with potassium persulfate decrease both the reaction rate and the average molecular weight. An even greater drop of reaction rate was noted when chlorine anions (TiCl3) were present. The presence of these ions had a stabilizing effect on the polydispersity.
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  • 78
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1471-1479 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectroscopy was done at different temperatures on epoxylated novolac resin DEN 438 (Dow Chemical Co.) alone, and after curing with various metal(II) phthalocyanine tetraamines (MPTA). Possible modes of fragmentation are given to explain the experimental results. Gas-chromatographic/mass-spectroscopic (GC-MS) analyses of MPTA derivatives indicated the presence of only trace quantities of benzene, aniline, cyanobenzene, and orthodicyanobenzene. The GC-MS studies of the cured DEN 438 epoxy resins indicated that the mechanisms of thermal degradation are qualitatively similar, and some common features were observed in their fragmentation in an electron beam and by thermal degradation. This study is a further assessment of the utility of these phthalocyanine derivatives for curing epoxy resins to produce heat-resistant polymer systems.
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  • 79
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1507-1514 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The initiation mechanism on the radical polymerization of vinyl monomers by polyethyleneglycol (PEG-300) in aqueous solution was studied. The initiating radical species were determined by means of the spin trapping technique. They were concluded to be generated by the hydrogen atom transfer from the monomer adsorbed at the ether group of PEG-300 to the free monomer.
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  • 80
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1535-1540 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereospecificity of benzyl derivatives of trivalent titanium (Rn TiX3-n, where X = Cl, I, n = 1-3) in butadiene polymerization was studied. It was found that dibenzyltitaniumiodide is an efficient catalyst of the 1,4-cis-polymerization of butadiene and that tribenzyltitanium forms 1,2-units. In both cases all the titanium-benzyl bonds participated in the initiation reaction and the active sites were polymeric analogues of crotyl derivatives of Ti(III); namely, bis-π-oligobutadienyltitaniumiodide and tris-π-oligobutadienyltitanium. These sites are stable at room temperature. The nature of the active sites in the polymerization of butadiene with Ziegler's 1,4-stereo-specific systems Til4 (or Til2Cl2) + AIR3 are described.
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  • 81
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1573-1578 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When 4-hydroxy-2,2,6,6-tetramethyl piperidinoxyl (HTMPO) is processed in polypropylene in a closed mixer, almost 50% is converted to other products during the first few minutes whilst the applied torque in the mixer is high. There is associated formation of unsaturation and this fact, in conjunction with the almost complete regeneration of nitroxyl within five minutes, suggests that the corresponding hydroxylamine (HTMPOH), which can be qualitatively identified, is the major transformation product. A study of the UV stability of PP films fabricated from polymer processed for varying times shows that UV stability is related to the quantity of the redox couple (HTMPO + HTMPOH) remaining in the polymer. This is considerably reduced by severe processing. The redox capable has almost no thermal antioxidant (oven aging) activity.
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  • 82
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1611-1621 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyamides 6.10 and 6.6 (PA* 6.10 and 6.6) containing small amounts of —N=N— units in the main chains were prepared by interfacial polycondensation between hexamethylenediamine and sebacoyl chloride or adipoyl chloride with addition of azobiscyanopentanoyl chloride. Polyamide-polystyrene block copolymers (PA-b-PSt) were then prepared by decomposition of the —N=N— units of PA*, initiating radical polymerization of styrene in m-cresol. The average PA block length of PA-b-PSt thus formed was longer than that expected from the initially present PA segments between the —N=N— units. This is probably due to recombination of PA radicals whose initiation efficiency is as low as 15%. The PSt blocks also had higher molecular weight (7000-79,000) in comparison with homopolystyrene produced from monomeric azobiscyanopentanoic acid used as an initiator due to higher viscosity of polymerization system. Variation of intrinsic viscosity and turbidimetric titration behavior along with the change in composition were also discussed.
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  • 83
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1603-1610 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of trimethylsilylacetylene was investigated by using W and Mo catalysts. Mixtures of WCl6 with appropriate organometallic cocatalysts such as n-Bu4Sn and Et3SiH at 1:1 molar ratio provided poly(trimethylsilylacetylene) in high yields. On the other hand, MoCI5 gave mainly methanol-soluble oligomers even in the presence of these cocatalysts. The polymer formed was a partly insoluble yellow powder, and the molecular weight of the soluble fraction was about 7000. The IR, 1H-NMR, and 13C-NMR spectra supported the polymer structure, (CH = CSiMe3)n. Protodesilylation of poly(trimethylsilylacetylene) afforded a new polymer containing both acetylene and trimethylsilylacetylene units.
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  • 84
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1733-1742 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cationic oligomerization of bicyclic oxalactam, 8-oxa-6-azabicyclo[3.2.1]octan-7-one [abbreviated as BOL (1)], was carried out at 0-60°C with trifluoromethanesulfonic acid and borontrifluoride etherate as catalysts to obtain the oligomer mixture at high yield. From the structural analysis of the isolated dimer, a N-(2(e)-carbamoyltetrahydropyran-6(e)-yl)-8-oxa-6-azabicyclo[3.2.1]octan-7-one, the oligomerization proceeded through the 5C-6N scission in (1) but not through the 6N-7C (amide group) scission as generally observed in common lactams. This peculiar oligomerization must result from the protonation to the oxamide unit in the BOL molecule.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1775-1782 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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  • 86
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1803-1815 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of aqueous polymerization of acrylamide with KMnO4/glycine redox pair was studied in an atmosphere of nitrogen at 35 ± 0.2°C. The rate of polymerization was found to be first power on monomer, activator, and catalyst concentration. The overall energy of activation was calculated to be 15.66 kcal/deg mol (65.54 kJ/mol) between 30 and 50°C. The effects of various additives (alcohols, neutral salts, complexing agents, addition of catalyst) were studied. The dependence of the polymerization rate on the activator and catalyst concentration was studied in DMF-water mixture also. The molecular weight of polymer was determined at various temperatures of the reaction medium.
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  • 87
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1743-1756 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several polyamides of p-phenylenedioxydiacetic acid (PDDA) were synthesized by the low-temperature solution polycondensation techniques. Six different diamines were condensed independently with p-phenylenedioxydiacetyl chloride (PDC) in a mixture of N-methyl pyrolidone (NMP) and hexamethyl phosphoramide (HMPA). The polymers were obtained in 80-95% yield and possessed inherent viscosities in the range 0.32-0.81 dL/g. The polymers were characterized by infrared (IR) and H1-NMR spectra. The solubility, density, crystallinity, and thermal stability of the polyamides were also determined. A model diamide (MDA-1) was also synthesized from aniline and PDC to confirm the formation of polyamides from diamines.
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  • 88
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1797-1801 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation degradation of viscoelastic solutions of a dialkyl monohydroxy aluminum polymer compound (AIR2OH)x is investigated. Radioactive cobalt-60 is chosen for irradiation experiments. The viscosity of the polymer in six different solvents is measured after irradiation using a capillary viscometer at room temperature (25°C). The degradation effects on both the radiation dose and the solvent used.
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  • 89
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    Topics: Chemistry and Pharmacology
    Notes: Asymmetric selective (or stereoelective) polymerization of racemic 1,2-diphenylethyl methacrylate (DPEMA) with ethylmagnesium bromide (EtMgBr)-(-)-sparteine catalyst was studied in toluene at -78°C. In the polymerization (S) enantiomer was consumed preferentially and the enantiomeric excess of initially polymerized (S) enantiomer was consumed preferentially and the enantiomeric excess of initially polymerized DPEMA was greater than 90%. Optically pure (R) monomer was recovered at about 70% polymer yield. Poly(DPEMA) obtained with EtMgBr-(-)-sparteine complex was highly isotactic. It was found in the polymerization of optically active DPEMA that optical rotation of poly(DPEMA) was dependent on the tacticity and that isotactic and syndiotactic poly(DPEMA)s showed opposite optical rotations. Circular dichroism spectra of the optically active polymers were measured.
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  • 90
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1865-1873 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The laser-initiated polymerization of a thiol-ene photopolymerizable system was studied. The laser was operated in single- and multiple-pulse modes to generate exotherms, which were measured in a modified differential scanning calorimeter. Arrhenius plots of the polymerization, obtained by measuring polymerization exotherms at various temperatures, showed positive and negative portions. Pseudoactivation energies for the thiol-ene polymerization increased rapidly at low conversions (〈50%) of the thiol and ene chromophores. The results were comparable to those obtained from photopolymerization of multifunctional acrylate monomers.
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  • 91
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1909-1921 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: By exposure to ultraviolet and gamma radiation and by the usual methods of thermal polymerization, the stereospecific polymerization of methyl aryloxymethacrylates was carried out at different temperatures in several solvents. Triad tacticity values of the polymers obtained by free-radical and ionic routes were computed from nuclear magnetic resonance spectral data. Results of this investigation support our earlier observationSee: K. Saunders, T. Balakrishnan, R. W. Lenz, and K. Hatada, Macromolecules, 12, 392 (1979). that, under the conditions used, heterotactic content is the maximum in most of these polymers, thereby justifying the high steric effect of the bulky and polar aryloxy side chain which offers equal isotactic and syndiotactic placements.
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  • 92
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1987-1996 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cationic, ring-opening polymerization of 1,6-anhydro-3,4-di-O-benzyl-2-deoxy-β-D-arabino-hexopyranose (ABDA) (=1,6-anhydro-3,4-di-O-benzyl-2-deoxy-β-D-glucopyranose) was investigated with Lewis acid as catalyst. Phosphorus pentafluoride at -78°C caused polymerization to a highly stereoregular (1 → 6)-α-linked polysaccharide. Effects of C-2 substituent on the polymerization of 1,6-anhydro sugar are discussed. In addition, copolymerization of ABDA (M1) with 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose (LGTBE, M2) was studied. The monomer reactivity ratios calculated by the Kelen-Tüdös method were r1 = 4.46 and r2 = 1.66. Debenzylation of the polymer produced 2-deoxy-(1 → 6)-α-D-arabino-hexopyranan in which every repeating unit contained two free hydroxyl groups.
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  • 93
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2381-2393 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absolute rate constants for propagation (kp) and for termination (kt) of ethyl α-fluoroacrylate (EFA) were determined by means of the rotating sector method; kp = 1120 and kt = 4.8 × 108 L/mol.s at 30°C. The monomer reactivity ratios for the copolymerizations with various monomers were obtained. By combining the kp values for EFA from the present study and those for common monomers with the monomer reactivity ratios, the absolute values of the rate constants for cross-propagations were also evaluated. Reactivities of EFA and poly(EFA) radical, being compared with those of methyl acrylate and its polymer radical, were found to be little affected by the α-fluoro substitution. Poly(EFA) prepared with the radical initiator was characterized by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Although the glass transition temperature obtained by DSC for poly(EFA) resembled that of poly(ethyl α-chloroacrylate), its TGA thermogram showed fast chain de polymerization to EFA that was distinct from complicated degradation of poly(ethyl α-chloroacrylate).
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  • 94
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    Topics: Chemistry and Pharmacology
    Notes: A polymethacrylate derivative containing uracil bases was methylated by using methyl iodide or dimethyl sulfate to give polymers containing 3-methyluracil derivatives. In the case of methylation with dimethyl sulfate, sulfonation at 5-position of the bases occurred in addition to the methylation at N-3 position. The methylated polymers thus obtained were used further for the study of polymer complex formation with polymethacrylate containing adenine base.
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  • 95
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2523-2531 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyelectrolyte submicron microcapsules were prepared by interfacial crosslinking of an aqueous salt solution of poly(ethyleneimine) and a toluene solution of brominated poly-(2,6-dimethylphenylene oxide). The two solutions were brought together and mixed by sonication. As a result, a stable emulsion was obtained, which was subsequently cast into a membrane in which the microcapsules were embedded. The salt solution contained in the microcapsules could be released under controlled conditions. The rates of release were measured. They could be controlled by applying osmotic pressures, by additional quaternization of the membrane, or by modification of the structure of the capsule wall by introduction of a surfactant.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2539-2550 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A combined (chemical and infrared (IR) spectrophotometric) method is discussed for the simultaneous determination of concentrations of carboxyl (A), ketone (K), and ester (E) groups formed in the oxidation of polyethylene (PE). The IR absorptivities of these functional groups were determined by using model compounds [stearic acid, stearone, poly-(1,4-butylene sebacate)]. The integral absorption of the C=O band of polymer samples which contained several oxo groups of different types was found to be additive. This method was applied to the determination of the carboxyl, ester, and ketone content of samples oxidized at different oxygen pressures.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2579-2599 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyamides and related model compounds were prepared from carboxy acids and primary amines by reacting them with triphenylphosphite in an appropriate solvent at 100°C. The reactions proceeded in the absence of organic base but were accelerated by the addition of bases such as pyridine. Nevertheless, even the powerful combination of 13C and 31P NMR failed to indicate the presence of pyridinium phosphite in the reaction mixture. In the reaction of a primary amine and carboxyl groups a detectable amount of the diphenoxy aminophosphine intermediate was observed. The end products are the amides, phenol, and diphenyl phosphite. When primary amine was not present a slow formation of a phenyl ester of the carboxylic acid was evident. All the intermediate species and the end products were formed with or without added pyridine. A mixed anhydride of carboxylic acid and phosphite was never seen. The results in this article are fundamentally the same as those in the companion article (I) for which the data were obtained at 280°C in the absence of solvent and base. However, because the reaction went quickly to completion at 280°C, the diphenoxy aminophosphine intermediate was not observed. A mechanism for the amidation in which the diphenoxy aminophosphine is an initial reaction intermediate is proposed. This species reacts with the carboxylic acid through an intramolecular substitution to give an amide. This mechanism may be valid for the high-temperature reactions as well. Several minor unclear points are indicated.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2661-2666 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESCA has been used to investigate the composition and structural features of plasma-polymerized 2,4,6-trifluoro-1,3,5-triazine. Polymer formation was studied as a function of power and post-polymerisation treatment. All the polymer films revealed an intense peak at a binding energy of ∼290.2 eV probably arising from groups. A high sensitivity towards hydrolysis was observed resulting in substantial loss of fluorine and increase in oxygen content of the plasma polymers.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2685-2697 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of chain transfer to the bifunctional initiating and transfer agents (binifers) 1,4-di(2-chloro-2-propyl)benzene (p-DCC), 1,3-di(2-chloro-2-propyl)-5-tert-butylbenzene (m-tBuDCC), and 1,3-di(2-chloro-2-propyl)-4,6-dimethylbenzene (m-DMeDCC) in the polymerization of isobutylene has been investigated. Chain transfer to monomer was shown to be absent up to -20°C in CH3Cl/n-hexane and CH2Cl2/n-hexane mixtures using the m-tBuDCC/BCl3 binifer system. Chain transfer constants (Ci) to m-tBuDCC and kt/kp ratios determined in the range from -30°C to -80°C in CH3Cl/n-hexane mixtures and pure CH3Cl solvent are reported, and the activation energy differences Etr,l - Ep and Et - Ep were calculated. Chain transfer constants to p-DCC and m-DMeDCC were determined by the use of pure CH3Cl diluent at -50°C. The chain transfer reactivity of five different inifers is discussed and compared based on CI values obtained under identical conditions, with special regard to the new, sterically hindered binifer m-DMeDCC of extraordinary reactivity.
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    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2945-2952 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Influences of microenvironment of various polyelectrolytes, i.e., ionene polymers and polyamine sulfones, on the photo- and/or thermal isomerization between the trans and cis forms of sodium m-(4-ethoxyphenylazo)benzene sulfonate (SEPS) were studied. 6,6-Ionene demonstrated larger enhancing effect on the cis-trans thermal isomerization than 3,3-ionene, which indicated that the micropolarity or the pH around the polymer is important. In the Arrhenius plots for both photo- and thermal isomerizations, deviations from the linearity were observed. In the former case, a sharp bend and the negative apparent activation energy were obtained at the high temperature. Furthermore, they were sensitively affected by the polyelectrolytes.
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