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  • Articles  (16)
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  • Wiley-Blackwell  (16)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 735-742 
    ISSN: 0887-6266
    Keywords: poly(3-alkylthiophene) ; whiskers ; crystallization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that poly(3-alkylthiophene)s may readily crystallize from poor solvents in the form of whiskers. The experimental conditions required for the formation of whiskers were found to depend upon the alkyl side-chain length, solvent quality, and temperature. In all cases studied for alkyl side-chain lengths of 3-12 carbon atoms, the widths of the whiskers were of the order of 15nm, while their lengths often exceeded tens of microns. The thickness of the whiskers formed under the experimental conditions employed was found to scale with side-chain length, and was approximately 2 or 3 times the a/2 lattice dimension of the polymer unit cell. Packing of the macromolecules within the whiskers was such that the polymer backbones were normal to the whisker length; that is, the b-axis was oriented parallel to the long axis of the whiskers. These results are thought to be relevant to known thermochromism phenomena associated with poly(3-alkylthiophene)s. © 1993 John Wiley & Sons, Inc.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1383-1393 
    ISSN: 0887-6266
    Keywords: self-nucleation ; crystallization ; melting ; isotactic polypropylene ; thermal analysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization behavior after partial or complete melting of the α phase of iPP is examined by combined differential scanning calorimetry (DSC) and optical microscopy: calorimetric results are directly correlated with corresponding morphologies of microtome sections of DSC samples. On partial melting at various temperatures (hereafter referred to as Ts) located in a narrow range (4°C) below and near Tm, the number of nuclei increases (as in classical self-nucleation experiments), by several orders of magnitude; on subsequent cooling, the crystallization peak is shifted by up to 25°C. After partial melting in the lower part of the Ts range and recrystallization, the polymers display a prominent morphology “memory effect” whereby a phantom pattern of the initial spherulite morphology is maintained.After partial melting in the upper part of the Ts range the initial morphology is erased and self-nucleation affects only the total number of nuclei. The present experimental procedures make it possible to define, under “standard” conditions, the crystallization range of the polymer and in particular, the maximum crystallization temperature achievable when “ideally” nucleated. © John Wiley & Sons, Inc.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 573-577 
    ISSN: 0887-6266
    Keywords: crystallization ; nucleation ; spherulites ; liquid-liquid phase separation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization of poly(butylene terephthalate) (PBT) from moderately dilute solutions of PBT in a diglycidyl ether of bisphenol-A epoxy has been investigated. PBT dissolves in this epoxy approximately 35°C below its usual melting temperature of 227°C to form a one-phase solution. Cooling this solution below 165°C leads to rapid crystallization of the PBT. The resulting mixture of liquid epoxy and crystalline PBT has a low viscosity and contains highly birefringent, individual PBT spherulites. The PBT spherulites have a narrow size distribution and a high surface-to-volume ratio. These particles are suggested to arise from a rapid crystallization that follows liquid-liquid phase separation. © 1994 John Wiley & Sons, Inc.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 265-271 
    ISSN: 0887-6266
    Keywords: Nylon-12 ; dielectric properties ; crystallization ; calorimetry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric properties of 30% crystalline dry Nylon-12 have been measured over the frequency range 10-105 Hz and temperature range 300-450 K, and the effect of its annealing at 423 K investigated both by dielectric measurement and differential scanning calorimetry. Annealing causes its crystallization to α phase, which increase the dc conductivity and decreases the contribution to orientation polarization, but does not alter the shape of the relaxation spectrum. The orientation polarization in Nylon-12 involves two processes, each of which occurs above the glass-transition temperature of Nylon-12, but only the spectra of the lowest temperature process could be clearly resolved. © 1993 John Wiley & Sons, Inc.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 901-915 
    ISSN: 0887-6266
    Keywords: poly(aryl ether ketones) ; poly(ether imide) ; crystallization ; melting ; glass transition ; morphology ; small-angle x-ray scattering ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relationships among glass transition, crystallization, melting, and crystal morphology of poly(aryl ether ketone) (PAEK)/poly(other imide) (PEI) blends was studied by thermal, optical and small-angle x-ray scattering (SAXS) methods. Two types of PAEK were chosen for this work: poly(aryl ether ether ketone), PEEK, and poly(aryl ether ketone ketone), PEKK, which have distinctly different crystallization rates. Both PAEKs show complete miscibility with PEI in the amorphous phase. As PAEK crystallizes, the noncrystallizable PEI component is rejected from the crystalline region, resulting in a broad amorphous population, which was indicated by the broadening and the increase of Tg over that of the purely amorphous mixture. The presence of the PEI component significantly decreases the bulk crystallization and crystal growth rate of PAEK, but the equilibrium melting temperature and crystal surface free energies are not affected. The morphology of the PEI segregation was investigated by SAXS measurements. The results indicated that the inter(lamellar-bundle) PEI trapping morphology was dominant in the PEEK/PEI blends under rapid crystallization conditions, whereas the interspherulitic morphology was dominant in the slow crystallizing PEKK/PEI blends. These morphologies were qualitatively explained by the expression δ=D/G, where G was the crystal growth rate and D was the mutual diffusion coefficient. © 1993 John Wiley & Sons, Inc.
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  • 6
    ISSN: 0887-6266
    Keywords: crystallization ; nucleation ; nucleating additives ; isotactic polypropylene ; DSC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A simple, convenient and reliable calorimetric efficiency scale is proposed for the evaluation of nucleating additives for polymers. The scale is based on conventional differential scanning calorimetry cooling runs and makes use of a crystallization range determined in self-nucleation experiments. It can be correlated with spherulite sizes, and indicates the potential range of improvement of nucleating additives. Typical nucleating agents for isotactic polypropylene are evaluated; at best they rate at 60 to ca. 70% on this efficiency scale. © 1993 John Wiley & Sons, Inc.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1407-1424 
    ISSN: 0887-6266
    Keywords: isotactic polypropylene ; β phase ; α nucleation ; melting ; crystallization ; growth transitions ; thermal analysis ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanisms which, in isotactic polypropylene, create α phase nuclei on partial melting of β phase spherulites are investigated by thermal analysis and optical and electron microscopy. Nuclei concentrations are determined from recrystallization characteristics. α phase nuclei are formed within β spherulites via two different mechanisms: (1) a low temperature formation of latent α phase nuclei (αβ* nuclei) linked with a hitherto unsuspected β to α growth transition at T = T* ∼ 105°C, and (2) a high temperature α phase nucleation process (αβ nuclei), also linked with a similar β to α growth transition at 140°C first reported by Varga et al. The low temperature nucleation mechanism is the more efficient one: it significantly affects the melting of β phase, and results in samples with over 1013 α nuclei · cm-3. © 1993 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1627-1639 
    ISSN: 0887-6266
    Keywords: semi-IPN ; crystallization ; phase separation ; compatability ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential scanning calorimetry together with dynamic mechanical analysis were employed to investigate the crystallinity and the miscibility in poly(ethylene oxide)/crosslinked poly(methyl methacrylate) semi-IPN (interpenetrating polymer networks). The crystallinity of poly(ethylene oxide) in the semi-IPN is found to depend on the crosslink density of PMMA as well as the overall content of PEO. Of special interest is that an increase in the crosslink density tends to increase the crystallinity contrary to our expectation, indicating crystallization and phase separation may proceed simultaneously during IPN formation. The investigation of glass transition behaviors with dynamic mechanical analysis suggests phase separation (i.e., there exist two amorphous phases: one PEO-rich phase, the other a PMMA-rich phase). © 1993 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1183-1190 
    ISSN: 0887-6266
    Keywords: polyamide ; aliphatic ; crystallization ; binodal ; ternary ; phase diagram ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Concentration-dependent ternary interaction parameters are experimentally determined for the polyamide homopolymers, Nylon-6, -66, -610, and for the Nylon-66/610/6 terpolymer in formic acid-water systems. The binodal envelope, the tie lines, and the crystallization isotherms at 25°C are given for each of the ternary systems. © 1994 John Wiley & Sons, Inc.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1991-1998 
    ISSN: 0887-6266
    Keywords: polypropylene (PP) ; blend ; compatibilization ; crystallization ; fractionated crystallization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The compatibilization of incompatible polypropylene (PP)/poly(ethylene oxide) (PEO) blends was studied. The experimental results showed that the graft copolymer [(PP-MA)-g-PEO] of maleated PP(PP-MA) and mono-hydroxyl PEO (PEO-OH) was a good compatibilizer for the PP/PEO blends in which PP-MA also had some compatibilization. The crystallization of the blends was affected by the compatibility between PP and PEO. The interfacial behavior of the compatibilizers had an important effect on crystallization behavior of the PP/PEO blends. PEO showed fractionated crystallization in the PP/PEO blends. This behavior was studied from the view point of the theory of fractionated crystallization. © 1994 John Wiley & Sons, Inc.
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  • 11
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2585-2594 
    ISSN: 0887-6266
    Keywords: PEKK ; copolymer ; terephthalate/isophthalate ; structure ; crystallization ; melting ; x-ray diffraction ; thermal analysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In a previous study, we have investigated the structure, crystallization, and morphology of poly(aryl ether ketone ketone), PEKK, copolymers prepared from diphenyl ether (DPE), terephthalic acid (T), and isophthalic acid (I) with T/I ratios from 100/0 to 50/50. These materials were considered as having -DPE-T-DPE-T- (TT) and/or -DPE-T-DPE-I- (TI) “phthalate diads.” In this work, we continue the study of this copolymer series with six different T/I ratios (40/60, 30/70, 20/80, 15/85, 10/90, and 0/100), which are viewed as having TI and/or -DPE-I-DPE-I- (II) “diads.” The I moieties (1,3-linked isomers) were always found to be incorporated in the crystals and acted as “entropy or symmetry” defects that effectively decreased the equilibrium melting temperature Tmo and the rate of crystallization. However, the retardation of crystallization in PEKK 0/100 (the homopolymer with pure II diads) was significantly less than expected, which was attributed to the segregation of I moieties between the chains leading to a reduction of total entropy in the unit cells. The evidence of segmental segregation in PEKK 0/100 was seen in x-ray diffraction patterns, where several extra reflections were seen that could only be indexed by the published unit cell modified with a larger c-axis dimension (3.048 nm, corresponding to the length of six phenyl residues or 1.524 nm, the length of three phenyl residues). The composition of 15/85 was found to have the lowest value of Tmo and the slowest crystallization rate. Upon heating, the “II” crystals (T/I from 30/70 to 0/100) exhibited the conventional double-melting behavior rather than the triple-melting behavior as in the “TI” crystals (50/50 to 40/60). No indication of the second polymorph form 2 was found in “II” crystals. © 1994 John Wiley & Sons, Inc.
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  • 12
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 201-204 
    ISSN: 0887-6266
    Keywords: poly[styrene-b-(ethylene-co-butylene)-b-styrene] ; poly (vinylidene fluoride) ; miscibility ; crystallization ; melting ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: No Abstract
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  • 13
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1285-1291 
    ISSN: 0887-6266
    Keywords: crystallization ; isotactic polypropylene ; high-density polyethylene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The melting behavior of spherulites in thin sections of isotactic polypropylene bulk samples and high-density polyethylene thin films crystallized isothermally at various temperatures has been studied by polarized light microscopy. The regions around cavities and multiple boundary points between spherulites have higher melting temperatures than the other parts of spherulites crystallized in Regime III. The increase in melting temperature is explained as a result of crystallization under negative pressure arising locally in pockets of occluded melt due to density change during spherulitic crystallization. The negative pressure lowers locally the equilibrium melting temperature and therefore decreases the undercooling, which results in an increase in lamellar thickness. Sectioning of bulk samples releases frozen negative pressure and reveals the increase in melting temperature of those parts of spherulites that were crystallized at lower undercooling. © 1993 John Wiley & Sons, Inc.
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  • 14
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 961-968 
    ISSN: 0887-6266
    Keywords: silk fibroin ; β structure ; crystallization ; molecular conformation ; glass transition ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Structural changes of native and regenerated silk fibroin membranes were induced by immersion in water-methanol solutions and examined as a function of immersion time and methanol concentration. X-ray diffractometry and infrared spectroscopy data showed that transition from random coil to β-sheet structure occurred favorably when both native and regenerated silk fibroin membranes were immersed in water-methanol solutions, regardless of the different immersion time. Only native silk membrane, treated for 2 min with pure methanol, maintained its original amorphous structure, as demonstrated by differential scanning calorimetric (DSC) curves. The degree of displacement, measured by thermomechanical analysis (TMA), was much greater for regenerated than for native silk fibroin membranes. SDS-PAGE pattern showed that native silk fibroin has a molecular weight of 350, while the regenerated sample is formed by a large number of polypeptides in the range of 200-50 KD. The amount of acidic and basic amino acids decreased slightly in regenerated silk fibroin. Physical properties of silk membranes treated with water-methanol solutions are discussed in terms of membrane structure, treatment conditions, and chemical structure of starting material. © 1994 John Wiley & Sons, Inc.
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  • 15
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1999-2003 
    ISSN: 0887-6266
    Keywords: polytridecanolactone ; specific heat capacity ; melting ; crystallization ; transition enthalpy ; differential scanning calorimetry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An investigation of the thermodynamical properties of polytridecanolactone (PTDL) was made with the aid of a differential scanning calorimeter (DSC). PTDL is a linear polyester and belongs to the polylactones, which have been poorly investigated. In this paper we contribute with specific heat capacity in the range 180-400 K, and melting and glass transition characteristics. Further, we present unique results corresponding to the effect of different cooling rates on crystallization temperatures and crystallization energies. PTDL has a melting temperature of 350 K, and a glass transition at about 237 K. The crystallization results show that PTDL crystallizes easily, with a crystallization degree of about 80%. In addition, the crystallization energy decreases with increasing cooling rate, and levels out at a constant value at higher cooling rates. The crystallization temperature, on the other hand, shows an increasing sensitivity of cooling rate, where the supercooling is increasing more rapidly at higher cooling rates. © 1994 John Wiley & Sons, Inc.
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  • 16
    ISSN: 0959-8103
    Keywords: copolymers ; ethylene ; α-olefins ; transition metal catalysts ; thermal stability ; crystallization ; 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: Copolymers of ethylene with propylene, butene-1 and hexene-1 were prepared using a titanium-magnesium (TMC) or a vanadium-magnesium catalyst (VMC). The copolymers were examined for thermal stability by TGA, melting and crystallization behaviour by DSC and crystallinity by XRD. Fractionated samples of ethylene-hexene-1 copolymers were also similarly characterized. Results indicate that VMC produces copolymers with a higher degree of crystallinity and greater compositional homogeneity than TMC.
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