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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 203 (1964), S. 513-513 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] After giving due consideration to the disadvantages of introducing still another form of notation into the already overburdened literature, it is felt that the abbreviation 'roc' to stand for reciprocal ohm-centimetre is a worthwhile addition. The M.K.S. form follows, that is, a[rom] = ...
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 101 (2000), S. 70-79 
    ISSN: 1432-2242
    Keywords: Key words Poa annua L. ; Genetic diversity ; RAPD ; Turfgrass weeds ; Selection pressure ; Analysis of molecular variance ; AMOVA ; POPGENE
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  The genetic diversity of Poa annua L.populations collected from western Oregon grass-seed fields was surveyed using 18 randomly amplified polymorphic DNA (RAPD) markers. Markers from 1357 individual plants from 47 populations collected at three sampling dates (fall, winter, and spring) for 16 sites were used to measure genetic diversity within and among populations. Site histories varied from low to high herbicide selection pressure, and some sites were subdivided by 3 years of differing post-harvest residue management. Gene diversity statistics, simple frequency of haplotype occurrence, and analysis of molecular variance (AMOVA) revealed the presence of significant variability in P. annua among sites, among collection dates within sites, and within collection dates. Nei gene-diversity statistics and population-differentiation parameters indicated that P. annua populations were highly diverse. Mean Nei gene diversity (h) for all 47 populations was 0.241 and total diversity (HT) was 0.245. A greater proportion of this diversity, however, was within (HS=0.209) rather than among (GST=0.146) populations. When populations were grouped by season of collection, within-group diversity was HS=0.241, while among-group diversity was GST=0.017. When populations were grouped by site, within-group diversity was HS=0.224, while among-group diversity was GST=0.087. The diversity among populations within season for fall, winter, and spring collections was GST=0.121, 0.142, and 0.133, respectively. Populations collected from fields with histories of high herbicide selection pressure showed low differentiation among collection dates, with GST as low as 0.016, whereas those collected from fields with low herbicide selection pressure showed greater differentiation among collection dates, with GST as high as 0.125. At high selection-pressure sites, populations were also lower in gene diversity (as low as h=0.155), while at low selection-pressure sites there was higher gene diversity (as high as h=0.286). The site to site variability was greater for the high selection-pressure sites (GST=0.107 or 69% of the total among-population variance), while the season of germination variability was greater at sites of low herbicide-selection pressure (GST=0.067, or 70% of the total among-population variance). High initial diversity coupled with a long-term re-supply of genotypes from the seed bank must have been factors in maintaining the genetic diversity of this weed despite the intensive use of herbicides. Knowledge of the genetic diversity of Willamette Valley P. annua should help in formulating more effective strategies for managing this weed.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1933-1942 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Measurements described in this paper show that the effective water permeation coefficients of silver paste electrodes on polymers such as cellulose acetate are of about the same magnitude as those of the polymer itself and, therefore, that such electrodes will have negligible effect on moisture penetration when conditioning periods of several hours or longer are used. X-ray emission spectrography with Kα radiation from chlorine and potassium was employed to determine the salt content of 0.267-mm. cellulose acetate films (about 100 acetyl groups per polymer molecule = 40% acetyl), which were soaked for 48 hr. in aqueous solutions ranging up to 1M in concentration of the alkali chlorides or potassium halides. Typically, the salt contents are about 100 ppm or 3 μmole/g. of cellulose acetate. The actual salt contents are discussed in relation to ionic hydration, and Stokes' radii via the differential hydration energy concept of Samoilov and the phenomenological developments of Nightingale. The evidence suggests that ionic motion in moisture-swollen cellulose acetate is quite similar to that in aqueous solution.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 1197-1199 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The model of Fuoss and Boyd which interprets the Stokes' radius rs of an ion in solution as a sum (r + s/ε) of the ionic radius r and a dielectric interaction term s/ε is shown to be at least semiquantitatively applicable to alkali halides in aqueous solutions. Possible applications of the model to amorphous hydrophilic polymers are suggested. This note also contains several corrections to a previous paper.
    Additional Material: 1 Tab.
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  • 5
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The destruction of free radicals by oxygen diffusion into x-irradiated Lexan, [—O—C6H4—(CH3—C—CH3)—C6H4—O—(C=O)—]n, has been studied by means of optical and electron paramagnetic resonance measurements. Lexan, which is normally amber, appears uniformly green immediately after x-irradiation, but in a few hours, begins to bleach from the edges toward the interior, and a visible amber border forms about a green core. By direct measurements of the rate of recession of the boundary, it was found that the phenomenon is due to O2 diffusion and that the process obeys an Arrhenius expression (between 0 and 130°C.) with an activation energy of 0.31 e.v. (±3%). It has been shown that Zener's equation for the diffusion “frequency factor,” D0 = γS2v exp {ΛBE/kTm}, is useful in the study of diffusion in polymers even though it was derived for the case of atomic diffusion in metallic crystals. In the spectral region studied (0.3-0.7 μ) there are two bands (near 0.40 and 0.34 μ) present in the irradiated polymer which are not present in the unirradiated material. The center producing the absorption at 0.34 μ is stable over a long period. The absorption at 0.40 μ decays in a few days at room temperature when oxygen is present. At 250 Mcycles/sec. and 9000 Mcycles/sec. there was a single EPR absorption with a width of 13 ± 3 gauss, and at 250 Mcycles/sec., a g value of 2.012 ± 0.007. Measurements of changes in the spin concentrations with irradiation dose and sample age (measured from the instant of removal from the x-rays) showed that the color center which absorbs near 0.40 μ is paramagnetic. The radiation G value (at 40 k.v. and 18 kr/min.) for the paramagnetic centers was estimated to be about 5 spins/100 e.v. by comparison of the Lexan EPR spectrum with that of a DPPH spin standard. A simplified rate equation which was consistent with the decay data may be written: n = K'n/tα, where n is the average spin concentration as a function of time t and ≃ 1/2. The t-α factor can be interpreted in terms of a diffusion-limited supply of oxygen in the interior of irradiated Lexan.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 58 (1962), S. 553-570 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Optical techniques have been applied to study gas diffusion in poly(methyl methacrylate) and Lexan polycarbonate resin[poly(diphenyl-2,2-propane carbonate)] for temperatures ranging from 20°C. to the glass transition temperatures. One method consists of observing the movement of a sharp colored diffusion boundary which occurs when certain radical scavenging gases (e.g., O2, I2) penetrate a polymer which has been exposed to high energy irradiation. The theoretical basis and physical interpretation of the moving boundary are discussed. In essence, the color center concentration (produced by irradiation) is greater than the normal equilibrium concentration of scavenger molecules in the polymer so that the latter are trapped before they can move very far inward. The result is approximately a step-function distribution of the remaining color centers. For O2 penetration into Lexan below Tg, D (cm.2/sec.) ⋍ 0.014 exp {7100 cal./mole/RT}. This relation accounts for the effect of O2 partial pressure on the penetration rate. For O2 penetration into PMMA, below Tg, an activation energy of 10 kcal./mole was observed. A spectrophotometric method was used to measure the uptake of J2 vapor in polycarbonate films. The data indicate a large change (∼50 kcal./mole) in apparent activation energy near 114°C. Several possible applications of the moving boundary technique are mentioned and the results of its use to investigate the effect of stress on the diffusion rate in the polycarbonate are presented. Tensile stresses near the yield point produce a two-fold increase in D, whereas compressive stresses of comparable magnitude cause only a slight reduction.
    Additional Material: 13 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 15 (1977), S. 1199-1210 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of pressure on the thermal conductivity K of four vitreous poly(alkly methacrylate) polymers has been measured by steady state techniques. The measurements were made under pressures up to 2 kbar and over a temperature range between 173 and 300°K. For each member of the homologous series, K was found to increase with applied pressure. Shifts in thermal conductivity transition temperatures (attributed to glass transition phenomena) of 25, 26, and 16°C per kbar of applied pressure were observed for poly(methyl methacrylate), poly(ethyl methacrylate), and poly(n-isobutyl methacrylate).
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 359-363 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The temperature rise at the moving crack tip in poly(methyl methacrylate), resulting from the dissipation of the energy of crack propagation has been calculated. At velocities below 1 cm./sec., conduction of heat away from the crack plane into the bulk polymer appears to prevent any appreciable temperature increase.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 1097-1102 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This paper is a sequel to an earlier one on the applicability of classical nucleation theory to second-order transitions in the Ehrenfest sense (1). In each case the approach was to obtain the critical size rc and energy barrier ΔGc for the growth of a nucleus of β-phase in an α-phase matrix by a Maclaurin series expansion of the free-energy-density g = (Gβ - Gα)/vβ as a function of θ (in BC-I) and of ΔP and Δσ in this paper where θ = (T - Tt) is the degree of undercooling and ΔP and Δσ are analogous terms for the hydrostatic pressure shift and tensile stress shift away from the equilibrium transition. The expansion coefficients were determined by the use of thermodynamic relationships. For second-order transitions, rc = 4γvβ Tt/ΔCpθ2, rc = 4γ/Δβ(Δp)2, and rc = 4γ/YαYβ(Δσ)2, respectively, for the three cases. The terms ΔCp, Δβ, and ΔY denote the differences in heat capacity, compressibility, and Young's modulus, e.g., ΔY = Yβ - Yα. The interfacial energy γαβ is denoted by γ. The activation energy barriers for the cases developed in this paper were ΔGc = (16π/3)γ3/(Δβ)2 (Δp)4 and ΔGc = (64π/3)γ3Yα2Yβ2/(ΔY)2(Δσ)4. More complicated expressions are given in the paper for the rc and ΔGc for first-order transitions. In the long run, these expressions may prove more useful than the ones for second-order because of the modifications expressions for the kinetics of transformations.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 9 (1975), S. 253-254 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Additional Material: 1 Tab.
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