ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Physics  (5,206)
  • 1980-1984  (2,659)
  • 1970-1974  (2,547)
  • 1
    Unknown
    Amsterdam ; New York : North-Holland Pub. Co
    Keywords: DDC 530.1 ; LC QC20 ; Mathematical physics ; Physics ; Quantum theory ; Relativity (Physics)
    ISBN: 9780444875853
    Language: English
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1-5 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of polymerization of 1,3-dioxolan and degradation of polydioxolan catalyzed by boron trifluoride etherate have been studied in methylene chloride solution. The S-shape kinetic curves is found to be due to the autocatalytic action of the macromolecules formed. Effective participation of macromolecules in the initiation process has been confirmed on the basis of the relationship of the rate constants of boron trifluoride etherate reactions with cyclic monomer and with the polymer chain as well as by the decrease of the induction period on addition of the polymer or its low molecular weight analog, methylal, to the polymerization system.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 41-53 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of graft copolymer on the demixing of solutions of two immiscible homopolymers and critical conditions for emulsion formation were studied. The graft copolymer used in the present work consists of one backbone poly(vinyl acetate) (PVAc) and one branch polystyrene (PS). PVAc and PS of various degrees of polymerization were used as immiscible homopolymers. The common solvent was benzene. When the concentration of homopolymer blend was not sufficiently higher than the critical concentration for demixing of the blend solution, no stable emulsion was formed, even when a considerable amount of graft copolymer was present, and the added graft copolymer merely reduced the demixing rate. However, as the blend concentration was increased, a stable emulsion could readily be obtained by addition of rather small amounts of graft copolymer. The radius of emulsion droplets was inversely proportional to the weight ratio of the graft copolymer to the dispersed component polymer, in accordance with the theoretical prediction. It was concluded that the emulsions were stabilized against coagulation by graft copolymer molecules fixed strongly as a monolayer on the interface of the emulsion.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 89-104 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structure of the tetrameric dianion formed by α-methylstyrene in tetrahydrofuran by reaction with sodium has been examined. Mass spectral, NMR, infrared, and kinetic data all indicate that the structure is rather than the structure which had previously been assumed for this species.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 163-173 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A ziegler-type catalyst system consisting of tungsten hexachloride and alkyl or aryl tin compounds was found to polymerize cyclopentene and other cyclic olefins through a ring-opening mechanism. This catalyst system also polymerized α-olefins such as ethylene and 1-octene. An attempt was made to copolymerize cyclopentene and ethylene. Other catalyst systems were also employed for ring-opening polymerizations with limited success.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 175-189 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Separations of carboxyl-terminated polybutadiene (CTPB) liquid polymer according to functionality have been effected by using stepwise elution from silica gel. Recoveries in the 90-95% range have been achieved by deactivating the silica gel and recycling the unfractionated portion through progressively more active silica gel. Subjection of the fractions obtained from the silica-gel separation to analysis via gel-permeation chromatography and infrared spectroscopy yields not only functionality distribution data, but also provides an estimation of the relationship between molecular weight distribution and functional type. Repetitive analyses indicate a precision of ±7% (or less) of the amount of each functionality type present. An evaluation has been made of the accuracy of the data by fractionating saturated and methyl ester derivatives of CTPB under test conditions different from those employed in fractionating the original polymer. Within the known experimental error of the techniques employed, these studies have confirmed the data generated for CTPB polymer as received. Analytical techniques and interpretation of data are discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 191-201 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method has been developed for determining simultaneously the molecular weight of a broad-distribution polymer and the Mark-Houwink coefficients for that polymer type by using only GPC and intrinsic viscosity data. Standardized samples of poly(vinyl chloride), polystyrene, polybutadiene, and an experimental cycloolefin polymer were analyzed by this method. Shear-corrected intrinsic viscosities were used in all cases because of the high molecular weights involved. Molecular weight data for all samples were found to be in good agreement with molecular weight data obtained by membrane osmometry and from other GPC techniques. The proposed technique provides a means for calculating the molecular weight of a single polymer sample through universal calibration of GPC without knowledge of the Mark-Houwink coefficients for that polymer type.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 225-231 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nature of substitution in a slurry-phase chlorination of high-density polyethylene was studied using NMR and IR spectroscopy. The ratios of γ (or greater) methylenes were obtained from the NMR at different chlorine levels and compared with the theoretically predicted values based on a statistical treatment for substitution polymers. The results indicted that, unlike chlorosulfonated polyethylene, chlorinated polyethylene shows a hindered-type substitution. Molecular weight of the parent polyethylene, the degree of chlorination and the degree of residual crystallinity of the samples have no bearing on the type of substitution.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 253-259 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polybutadiene of high molecular weight was prepared in hydrocarbon solvent by using n-BuNa-tert-BuOM (M = Li, K) as a polymerization initiator. The microstructure of this polymer varied from 35 to 76% of 1,2 content, depending on the type of modifiers. The kinetics of polymerization was not studied, primarily due to the heterogeneous nature of the catalyst. However, other variables, such as the catalyst concentration and temperature, have been studied. The results and mechanistic implications are discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 241-251 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A single-charge emulsion polymerization involving a monomer which is a good solvent for its polymer is considered. It is shown to be unlikely that within the polymerizing latex particles there are concentration gradients large enough measurably to affect the kinetics of the reaction. The average displacement of monomers due to Brownian motion within the latex particles and in the absence of concentration gradients is calculated. This diffusive mean free path, corresponding to an interval involving less than 1% change in conversion, is shown to be much longer than the radius of the latex particle. Consequently, loci where monomer concentration is perturbed by conversion to polymer are immediately swamped by unreacted monomer. Also, direct experimental evidence exists showing that the monomer concentration in latex particles is about the same when nonpolymerizing latex particles are saturated or during polymerization in the presence of monomer excess. The thermodynamics of saturation swelling preclude the possibility of the existence of large concentration gradients. The arguments that have been advocated in the literature for core-skin separation within polymerizing latex particles were based on conversion data which were thought to be linear with time, while a reexamination indicates that they were not. The observed core-skin separation obtained when butadiene or tritiated styrene were copolymerized with styrene in the presence of a polystyrene homopolymer seed latex has questionable relevance to single-charge homopolymerization. There are reasons to doubt that the distribution of co-monomers within latex particles can be frozen by their conversion to polymers in a two-stage emulsion polymerization.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 275-278 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An analysis of the kinetic equation proposed for donor-acceptor systems indicated that the polymer yield at a given time should attain limiting value with increase in rate of initiation. It was essential that the equilibria not be shifted by temperature variation, and the change in rate of initiation was achieved by controlled current passage through the solution. A definite plateau in the yield of polymer was obtained. This was shown not to be due to diffusion control of the rate of initiation.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 301-303 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 311-313 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 319-326 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers with alternating dioxysilphenylene and diorganosilane units were investigated as a source of high-temperature elastomers for the aerospace industry. A copolymer with dimethylsilane units alternating with dioxysilphenylene had a glass transition temperature of -63°C and exceptional thermal stability; a polymer with diphenylsilane units alternating with dioxysilphenylene had a glass transition temperature of 0°C and slightly higher thermal stability. Both were cured to elastomers at room temperature with ethyl silicate in combination with dibutyltin diacetate. Both had tensile strengths (ultimate) above 4000 psi even without reinforcing fillers. Reinforced elastomers of the dimethyl copolymer had tensile strengths (ultimate) up to 16,000 psi.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 327-343 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Certain copolymers of maleimide and N-substituted maleimides yield brilliant colors when treated with sufficiently strong basic reagents under nonhydrolytic conditions. For color generation, the copolymer must be capable of HX elimination. The chromophores which account for color probably result from the ionization of acidic protons in structures involving one or more double bonds conjugated with imide carbonyl. The analogy to the color reactions of aconitylanil is pointed out. Spectra covering the range of 330-700 mμ are presented for a number of copolymer-amine color-generating systems. The colors produced in base with radical-initiated polymaleimide and imidazole-initiated poly-N-alkylmaleimides as well as the absence of color with anionic polymaleimide and radical poly-N-alkylmaleimides are discussed in light of what is known about their polymerization kinetics and mechanisms. Corresponding maleic anhydride copolymer systems are mentioned.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 637-648 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal degradation of model biscarbamates, polyurethanes and poly(urethane-ureas) has been investigated by pyrolysis at atmospheric pressure. The biscarbamates were prepared from phenyl, benzyl, and cyclohexyl isocyanate and ethylene glycol. The polyurethanes and poly(urethane-ureas) were prepared from tolylene diisocyanate (TDI), xylylene diisocyanate (XDI), and 4,4′-dicyclohexylmethane diisocyanate (H12-MDI) and poly(oxyethylene glycols) of various molecular weights. Rate constants for thermal degradation were obtained by measuring carbon dioxide evolution. The thermal degradation of all materials showed that the stability increased in the following manner: aromatic 〈 aralkyl 〈 cycloaliphatic. The separation and identification of the products of the thermal degradation gave an insight into the mechanisms involved in the pyrolysis of aromatic, aralkyl, and cycloaliphatic biscarbamates and the influence of temperature on these mechanisms.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 671-673 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 18
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 683-689 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 661-670 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermoplastic polyurethane elastomers incorporating the resin acid-derived 12-hydroxymethylabietanol (12-HMA) were prepared, and some physical properties are reported. A polyester macroglycol was prepared from 12-HMA, adipic acid, and ethylene glycol. This macroglycol then was combined with either poly(tetramethylene adipate) glycol (PTAd) or poly(ethylene adipate) glycol (PEAd) and 1,4-butanediol to give a glycol blend of 300 average hydroxyl equivalent weight (OHE). The glycol mixture then was combined with diphenylmethane 4,4′-diisocyanate (MDI) (NCO/OH = 1.0) to give urethane polymers soluble in tetrahydrofuran. Polymers were prepared with 0, 5, 10, 15, 20, and 25%, by weight, 12-HMA with PTAd as the other macroglycol and with 0, 10, 15, and 20% 12-HMA with PEAd as the other macroglycol. At 15% 12-HMA, polymers were made from glycol mixtures having 275 and 350 average OHE to demonstrate the effect of changing the hard-segment concentration. The presence of 12-HMA is shown to have its maximum effect on tensile properties at 15-20% in the PTAd series and at 10% in the PEAd series. In general, this effect is an increase in tensile strength and modulus and a decrease in elongation when compared with a similar polymer without the 12-HMA.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 20
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Equimolar reaction of Et2AlOLi and Et2AlCl gave Et2AlOAlEt2. The catalyst behavior for polymerization of acetaldehyde, propylene oxide, and epichlorohydrin was compared with that of the AlEt3-H2O (1:0.5) catalyst system. The thermal disproportionation product of Et2AlOAlEt2 derived from Et2AlOLi-Et2AlCl had the structure, —(EtAlO)n—, and it showed catalyst behavior quite similar to that of the product obtained by the same treatment of AlEt3-H2O (1:0.5). These ethylaluminum oxides can be regarded as species predominating in AlEt3-H2O (1:0.5) and AlEt3-H2O (1:1), respectively. Stereospecific or high molecular weight polymerizations of these species were investigated.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 21
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 723-735 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It was found that pyrrole, one of the active hydrogen compounds, easily condensed with formalin and amine in the presence of acid catalyst to yield a new type of polyamine polymer containing pyrrole nuclei in the main chain of the polymer. This polymerization method was also confirmed to be applicable to the other active hydrogen compounds, such as N-methylaniline, acetone, malononitrile, and hydroquinone. The structures of the polymers obtained were determined by infrared NMR and elementary analyses.We named this reaction a Mannich polymerization and the polymers obtained the Mannich base polymer.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 22
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 763-778 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interfacial condensation polymerization of optically active camphoryl dichloride and d,l-1,2-propylenediamine gave benzene-soluble and benzene-insoluble optically active polyamides. However, the recovered unreacted 1,2-propylenediamine was not optically active, and the selective condensation polymerization of 1,2-propylenediamine did not occur. The specific rotation of the benzene-soluble polyamide was positive, while that of the benzene-insoluble polyamide was negative. The results of proton magnetic resonance spectra suggested that the benzene-insoluble polyamide contained predominantly trans-camphoryl residues, while the benzene-soluble polyamide had predominantly cis-camphoryl residues. The difference in the specific rotation is believed to reflect the difference in relative reactivity between cis-camphoryl and the trans camphoryl residues. It was found that poly(l-methylethylene camphoramide) did not have a helical conformation in solution.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 23
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 789-799 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to discuss the electrostatic-field effect on a polymer reaction, the quaternization of poly-4-vinylpyridine-benzyl chloride (system I) was compared to that of poly-γ-chloromethylstyrene-γ-picoline (system II). In these two systems, the reaction initially proceeded according to the simple second-order kinetics. However, after the degree of quaternization exceeded 20-30 mole-%, a deviation from simple second-order kinetics occurred. In system I negative deviation occurred, while in system II positive deviation occurred. These phenomena occurred even though the solvent or the initial concentrations of the reactants were changed. The reasons for these phenomena are given below. In system I, the quaternized pyridine nitrogens prevented the benzyl chloride from approaching the unquaternized pyridine nitrogens. However, in system II the free γ-picoline was attracted by the quaternized chloro-γ-methyl site. Furthermore, the point at which the deviation occurred was determined by the degree of chloromethylation. All these results suggest that the effect of an electrostatic field must be presumed in these two systems.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 24
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 801-821 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polybenzyl has been synthesized from the benzyl compounds, chloride, methyl ether, and isopropyl ether by using stannic chloride as the Friedel-Crafts catalyst. The detailed structures of these polybenzyls have been determined by use of methods including elemental analysis, molecular weight determination, and infrared, ultraviolet/visible, and NMR spectra. The structure of these polybenzyls is globular with a high degree of branching. Thermal degradation was studied by using DTA and stepwise and isothermal degradation with analysis of both the volatile fraction and the residue. The activation energy for scissions was determined from changes in the molecular weight of the sample with time at a range of degradation temperatures of 340-440°C. The composition of the volatile fraction changed with both temperature and time of degradation. Thermal scission is directed to internal units and depends on the presence of weak links such as substituted anthracene units.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 25
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 833-852 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The initial stages of the photolysis of cellulose under vacuum can be followed by the gas production. A photolysis cell is described which allows a rigorous temperature control and gives a reproducible photolysis surface of the solid carbohydrate sample. A mass spectrometer was used to analyze the gases. To measure accurately the small amounts produced in a small volume requires careful calibration of this instrument, together with a fixed routine for the experimental procedure. Using this apparatus, we have photolyzed hydrocellulose under vacuum with 253.7 nm light. Only H2, CO, and CO2 were evolved, the rate of H2 production increasing to a constant value, that of CO increasing more slowly without becoming constant, and that of CO2 decreasing rapidly to a constant value. No induction periods were observed. The gas evolution was not caused by residual O2 or CO2 adsorbed on the polymer, but the rates were altered by leaving the photolyzed sample under vacuum overnight or heating the unphotolyzed sample under vacuum at 100°C. The rates of gas production increased markedly when the light filter was changed to allow a combined photolysis by 253.7 and 184.9 nm light. The results illustrate that stringent precautions must be taken to filter off the latter line in polymer photolyses with Hg arc light if the results are to be meaningfully interpreted in terms of 253.7 nm light photolysis. On photolyzing hydrocellulose previously boiled in NaOH solution, a larger H2 production rate and a smaller CO2 rate (compared with untreated hydrocellulose) were observed. It is suggested that this standard alkali treatment is the reason for the differences between our results and the results of the photolysis of cellulose reported in the literature.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 26
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 873-896 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The peroxidation of caprolactam has been studied at 84°C, 100°C and 120°C. The decomposition of the initially formed ε-caprolactam hydroperoxide was found to be catalyzed by adipic acid monoamide which is formed by hydrolysis of adipimide. This imide results from the decomposition of the hydroperoxide and was found to act as oxidation inhibitor. The molecular weights of the polyamides obtained by polymerizing the peroxidized caprolactam were found to decrease as the extent of peroxidation and thus the concentration of adipic acid monoamide and other decomposition products increased. In all of these polyamides the concentration of acidic functions was appreciably higher than that of the titratable amino endgroups.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 27
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 853-872 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl-type monomers containing the pyrrole ring, such as 2-vinylpyrrole (2-VPyrr), N-(pyrrol-2-yl)methylacrylamide (PMA), N-methyl, N-(pyrrol-2-yl)methylacrylamide (MPMA), 2-allylpyrrole (2-AP), β-(pyrrol-1-yl)ethyl vinyl ether (PEVE), 2-diallyl-aminomethylpyrrole (DAMP), and 3-(2-pyrrolylmethyleneimino)propene-1 (PIP) were synthesized by various reactions involving characteristic properties of the pyrrole ring. Radical homopolymerizations and copolymerizations of these monomers were studied. In the homopolymerization of conjugated monomers such as 2-VPyrr and PMA, chain transfer to the pyrrole-containing monomer was remarkable but not degradative. The copolymerization parameters, that is, the values of r1, r2, Q1, and e1 of 2-VPyrr, were determined to be 0.066, 0.69, 5.53, and -1.36, respectively in the copolymerization of 2-VPyrr (M1) with MMA (M2). The Q and e values of the monomers containing a heteroaromatic ring such as 2-vinylpyrrole, 2-vinylfuran, and 2-vinylthiophene were evaluated by the molecular orbital theory. The e value of PMA was found to be negative (-0.64) in the copolymerization with styrene, although e for acrylamide derivatives is generally positive. This may be explained by the intermolecular hydrogen bonding between the carbonyl group and NH group of PMA. That is, attraction or polarization of π-electrons in the vinyl group of PMA is weakened by such hydrogen bonding. From the results of copolymerization of 2-AP with various comonomers, the comonomers could be classified into three categories: class a monomers, in which both Q and e values are largely positive, can copolymerize with 2-AP; class b monomers, having small e values, homopolymerize and can not copolymerize with 2-AP; class c monomers, in which both Q and e values are small. The Q and e values of the comonomer must be largely positive in order to permit copolymerization with an allyl-type monomer.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 28
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 925-938 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate studies were done on the polymerization of propylene with the TiCl3-diethyl aluminum chloride catalyst system. The polymerization is initially first-order with respect to propylene concentration. There is a rapid rate decline in the initial period, during which time the reaction becomes functionally second-order. A physical explanation for this behavior has been adapted from the Avrami equation for crystal growth kinetics. A yield equation was developed which fits experimental data closely. Rate correlations show that the initial rate is exponentially related to the TiCl3/alkyl ratio. Water and other active hydrogen compounds reduce rate; hydrogen increases rate. A “bimetallic” mechanism is proposed which views catalyst activation as consisting of three equilibria, followed by a propagation step where an alkyl group is transferred to the growing chain, and a realkylation of the hydride that remains after the propagation step.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 29
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 939-960 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High-resolution magnetic resonance spectroscopy has been used to investigate three areas of novolac resin chemistry: first, the lifetimes of glycol species in formalin under acid and base conditions and the reactivity of methylene glycol towards alcohols; second, the in situ identification of novolac resin intermediates; third, the novolac-hexamethylenetetramine cure mechanisms. It is shown that the mean lifetime of a given glycol species is an order of magnitude shorter under basic conditions than under an acid of equal normality. The ratio of the equilibrium constants for the addition of methylene glycol to methanol, benzyl alcohol, and phenol was measured as 70:20:1. New reactive intermediates were discovered while monitoring the reaction of phenol and formalin. The reactions of various phenols with hexamethylenetetramine were studied, and short-lived benzoxazines were detected at 100-120°C whenever ortho hydrogen was available on the phenolic nucleus. The NMR peak assignments in the reaction sequence: benzoxazine, dibenzylamine, tribenzylamine, diphenylmethane are presented. Spectra of the very elusive p-benzylamines of 2,6-xylenol were recorded at 100-155°C. At 170°C, the lifetimes of these p-benzylamines are too short to afford proton resonance spectra. No evidence of hexahydrotriazine or (CH2 = N-CH2)3N type structures was found in 100 MHz NMR spectra of reaction mixtures of a phenol and hexamethylene-tetramine.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 30
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 989-1001 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methyl methacrylate (MMA) was polymerized by radical initiation at 90°C by its own preformed tactic polymers, i.e., conventional (c-PMMA), isotactic (i-PMMA), and syndiotactic (s-PMMA) PMMA, and also by a preformed 1:1 stereocomplex of i-PMMA and s-PMMA. The collected polymers were separated into two fractions by extraction with boiling acetone and characterized by 60 MHz NMR spectra and viscometry. Higher polymerization rates were obtained in the presence of stereo-regular PMMA than in the presence of c-PMMA. Moreover, it appeared that i-PMMA promoted the formation of s-PMMA, and conversely s-PMMA the formation of i-PMMA, especially in the initial stages of the reaction. A higher M̄v of the preformed polymer yielded a higher rate and a higher stereospecificity of the polymerization. No polymerization took place in the absence of performed PMMA. The results support a replica mechanism proposed by Szwarc, in which polymerization is preceded by a specific arrangement of monomeric units along the polymeric chain into a distinctive pattern. Such arrangement coupled with a strong tendency of the isotactic and syndiotactic species to associate may lead to the present stereospecific replica polymerization. This association is demonstrated by rapid gelation during polymerization and by lowering of reduced viscosity in very dilute mixtures of i-PMMA and s-PMMA in MMA.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 31
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 675-681 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 32
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 691-694 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 33
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of homogeneity of polymerization phase and monomer concentration on the temperature dependence of initial polymerization rate was studied in the radiation-induced radical polymerization of binary systems consisting of glass-forming monomer and solvent. In the polymerization of a completely homogeneous system such as HEMA-propylene glycol, a maximum and a minimum in polymerization rates as a function of temperature, characteristic of the polymerization in glass-forming systems, were observed for all monomer concentrations. However, in the heterogeneous polymerization systems such as HEMA-triacetin and HEMA-isoamyl acetate, maximum and minimum rates were observed in monomer-rich compositions but not at low monomer concentrations. Furthermore, in the HEMA-dioctyl phthalate polymerization system, which is extremely heterogeneous, no maximum and minimum rates were observed at any monomer concentration. The effect of conversion on the temperature dependence of polymerization rate in homogeneous bulk polymerization of HEMA and GMA was investigated. Maximum and minimum rates were observed clearly in conversions less than 10% in the case of HEMA and less than 50% in the case of GMA, but the maximum and minimum changed to a mere inflection in the curve at higher conversions. A similar effect of polymer concentration on the temperature dependence of polymerization rate in the GMA-poly(methyl methacrylate) system were also observed. It is deduced that the change in temperature dependence of polymerization rate is attributed to the decrease in contribution of mutual termination reaction of growing chain radicals to the polymerization rate.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 34
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1149-1156 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced polymerization of binary systems consisting of glass-forming monomer and glass-forming solvent in supercooled phase was studied. The initial polymerization rates were markedly affected by Tg (glass transition temperature) and Tv of the system (30-50°C higher than Tg), which turned to be functions of the composition. The composition and temperature dependence of initial polymerization rate in binary glass-forming systems were much affected by homogeneity of the polymerization system and the Tg of the glass-forming solvent. The composition and temperature dependences in the glycidyl methacrylate-triacetin system as a typical homogeneous polymerization system were studied in detail, and the polymerizations of hydroxyethyl methacrylate-triacetin and hydroxyethyl methacrylate-isoamyl acetate systems were studied for the heterogeneous polymerization systems; the former illustrates the combination of lower Tg monomer and higher Tg solvent and the latter typifies a system consisting of higher Tg monomer and lower Tg solvent. All experimental results for the composition and temperature dependence of initial polymerization rate in binary glass-forming systems could be explained by considering the product of the effect of the physical effect relating to Tv and Tg of the system and the effect of composition in normal solution polymerization at higher temperature, which was also the product of a dilution effect and a chemical or physical acceleration effect.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 35
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 823-832 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of anionic polymerization of pivalolactone with polystyrene dicarboxylates decreased with conversion, suggesting deactivation of the propagating chain end by precipitation of the polymer during polymerization. The presence of unreacted initiator was explained by slow initiation for formation of a living polymer of pivalolactone. Various factors affecting block efficiency were discussed, and high efficiency was obtained for the preparation of block copolymers containing a long pivalolactone segment by using more nucleophilic polystyrene dicarboxylates. Block copolymer of acrylonitrile and pivalolactone was prepared from polyacrylonitrile dicarboxylates.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 36
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1201-1212 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ferrocenylmethyl acrylate (I) and ferrocenylmethyl methacrylate (II) have been readily copolymerized with maleic anhydride in benzene-ethyl acetate solutions. Similarly, II has been copolymerized with both acrylonitrile and N-vinyl-2-pyrrolidone in benzene solutions to give higher molecular weight copolymers in high yields. In all cases azobisisobutyronitrile has been the initiator. Based on e values obtained, the metal carbonyl substituent acts as an electron-withdrawing group. Over a wide range of comonomers (N-vinyl-2-pyrrolidone, styrene, vinyl acetate, methyl acrylate, acrylonitrile, and maleic anhydride) I and II exhibit r1 values lower than (and r2 values higher than) similar copolymerizations with methyl acrylate or methyl methacrylate. Further more, the Q values found for I (0.03-0.11) and II (0.08-0.18) are smaller than those for methyl acrylate (0.46) and methyl methacrylate (0.74). Thus, I and II are less reactive than expected, presumably due to steric effects.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 37
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 905-907 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 38
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 909-909 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 39
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel polyamides from trans-4-octen-1,8-dioic acid (4-OD) and trans-2-trans-6-octadien-1,8-dioic acid (2,6-ODD) ad linear aliphatic diamines or piperazine were prepared in good yields by low-temperature polycondensation. The polymers obtained were investigated by infrared spectroscopy, x-ray diffraction, and differential scanning calorimetry. Polyamides from 4-OD show high molecular weights and crystallinities and Tm above 500°K, whereas those from 2,6-ODD are very weakly crystalline and decompose without melting in nitrogen at temperatures higher than 550°K. DSC studies revealed in the case of 4-OD polymers with odd diamines, a multiple peak phenomenon in the melting region, strongly dependent from the heating rate. Some hypotheses consistent with this behavior are briefly discussed, and it is concluded that the phenomenon arises from melt recrystallization occurring during the DSC scan.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 40
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 961-969 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C nuclear magnetic resonance spectra (13C-NMR) of poly(methyl acrylates) and poly(isopropyl acrylates) of various tacticities were measured at 25.1 MHz and analyzed. 13C-NMR spectra of model compounds for poly(methyl acrylate), poly(acrylic acid), and poly(sodium acrylate) were also determined. The spectra of the polymers were generally complicated owing to the splittings corresponding to triad, tetrad, or pentad placements, and the assignment for each peak was difficult. Groups of peaks were analyzed by triad or tetrad placements by assuming Bernoullian or first-order Markovian statistics.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 41
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1359-1378 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 10-Methylphenothiazine and p-(methylthio)anisole were compared to polymers which contained these donor molecules on the side chains of N-acyl-substituted polyethylenimines. Charge-transfer absorption spectra were compared for these donors with the acceptors: dichlorodicyanobenzoquinone, tetracyanoquinodimethane, tetracyanoethylene, and 2,4,5,7-tetranitrofluorenone. Benesi-Hildebrand plots show that the formation of the polymer complexes have 3 to 50 times higher equilibrium constants than those of the corresponding model complexes. This can be explained by complexing parallel to the polymer backbone. The polymer has the proper geometry for complexing (6.4 Å, repeat distance in the polymer backbone), and an acceptor molecule can therefore be inserted between two adjacent donor molecules for increased stability. Shifts of the absorption maxima to longer wavelength for some of the polymer complexes can be rationalized by the probability that in the polymer, an acceptor is sandwiched between two donors and thus forms 2:1 complexes; the extra resonance energy may shift the absorption maximum to longer wavelength. A second possible explanation is based on solvation of the complex which reduces the energy of the excited state. Polymers absorb mainly in the complex form. Model compounds absorb mainly by contact charge transfer, which is nonsolvated and thus occurs at higher energy or shorter wavelength. Extinction coefficients are higher for the model complexes than for the polymer complexes. Contact charge transfer, which can contribute in greater proportion to the model than to the polymer complexes, explains this. The amount of contact charge transfer can be calculated simply from the probability of a donor being in the solvent shell of an acceptor. Complex decomposition rates were determined based on measuring changes in the intensities of the charge-transfer absorption spectra. Dichlorodicyanoquinone complexes were unstable, while the other complexes were stable.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 42
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The behaviors of free radicals produced in polyethylene irradiated with ultraviolet light and electron beams were compared in connection with primary processes of radical formation and trapping regions of free radicals. In the case of irradiation with ultraviolet light, an ESR spectrum observed at -196°C immediately after irradiation is an eight-line spectrum due to alkyl radicals of the type —CH2—ĊH—CH3, while in the case of ionizing radiation, a six-line spectrum due to —CH2—ĊH—CH2— was observed. The former radicals are produced by the Norrish type I reaction of the carbonyl groups contained in the polymer, followed by radical rearrangement; and the latter are formed by dissociation of hydrogen atom from the excited state of the polymer or ion-molecular reactions. From the sensitivity to oxygen molecules, it was deduced that free radicals are trapped in amorphous regions after ultraviolet irradiation, but mainly in crystalline regions after irradiation with electron beams. Saturation studies of ESR spectra seem to support this conclusion.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 43
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1439-1442 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 44
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1443-1446 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 45
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1449-1463 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polycondensation of aromatic dihydrazidines (bisamidrazones) with 1,4,5,8-naphthalenetetracarboxylic acid or 1,4,5,8-naphthalenetetracarboxylic dianhydride in polyphosphoric acid led to high yields of soluble benzobistriazolophenanthroline polymers. Inherent viscosities in methanesulfonic acid of 0.25-2.51 dl g were recorded. Prior to polymer synthesis, a series of model compounds were prepared by reactions analogous to the polycondensation reaction. The polymer structure was established by elemental analysis and spectral comparisons of the polymers with model compounds. The thermal properties of the polymers were studied by thermal gravimetric analysis, differential thermal analysis, differential scanning calorimetry, and softening under load. Onset of breakdown in an air atmosphere occurs in the 440-450°C range. No softening under load was observed up to 450°C.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 46
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1119-1130 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Persistent electrical polarization (heterocharged electret formation) has been studied as a function of stereotacticity, crystallinity, and molecular weight in membranes of poly(vinyl alcohol) (PVA) prepared via different synthetic routes. Membranes of PVA-sodium polystyrenesulfonate (PSSNa) and PVA-poly(vinyl acetate) (PVAc) copolymers and PVA-PVAc-PSSNa were also investigated. The degree of persistent polarization a pure PVA membrane can support, was found to vary according to isotactic 〉 syndiotactic 〉 heterotactic triad concentrations. Increases in crystallinity tend to decrease persistent polarization, and such changes in crystallinity are probably responsible for the above observed order, since measurements of persistent polarization on noncrystalline PVA-PSSNa membranes were found to vary according to syndiotactic 〉 heterotactic 〉 isotactic with regard to the PVA. Within PVA-PSSNa membranes the presence of acetate groups reverses the behavior of PSSNa from anhancer to an inhibitor of electret formation. The results all support a model in which heterocharged electret formation involves an ion displacement in the direction of the applied field and stabilization of this ion displacement by local hydrogen bonding.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 47
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1157-1165 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Theory is developed to determine the effect of interchange reactions on nonequilibrium distributions of condensation polymers and their associated molecular weight averages. The analysis offers a method for determining the interchange rates of condensation polymers.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 48
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1673-1681 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition and hydrolysis of 2,2′-azobis(2-amidinopropane) were examined as functions of pH. The rate of decomposition decreased with increasing pH. The specific rates at 60°C were 3.85 × 10-5 1/sec at pH 0.90 and 2.5 × 10-5 1 see at pH ≥ 8.5. The hydrolysis in alkaline solution yielded 2,2′-azobis(2-carbamylpropane) which was stable to thermal decomposition. The relation between the specific rate of hydrolysis kh′ and the concentration of hydroxyl ion was obtained as kh′ = 4.0 × 10-2 [OH]0.50 1/sec at 60°C. In alkaline solution, the rate of hydrolysis was considerably larger than that of thermal decomposition. A mechanism for this hydrolysis is propesed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 49
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1939-1952 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of solvent on solution or interfacial polycondensations was investigated in terms of selectivity and control of functional groups such as amine or hydroxyl groups toward polycondensation reactions. Solution polycondensation of a mixture of resorcinol (RL) and m-xylyenediamine (m-XD) with isophthaloyl chloride was affected by solvents to such extent as to change the course of the polycondensation reaction, and hexamethylenephosphoramide (HMPA) caused the formation of amide-rich polymer, while tetrahydrofuran (THF) was a solvent favoring formation of a polyamide ester with a regular structure. Polycondensation of 3,3′-dihydroxybenzidine (DHB) with isophthaloyl chloride yielded exclusively a linear polyamide in HMPA solution, while with aldehyde as a solvent polyester was obtained owing to the preservation of the amine group. Thus, it was found that the course of polycondensation reactions of monomers having different functional groups could be controlled by selection of a suitable solvent.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 50
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced polymerization of cis- and trans-1,3,3,3-tetrafluoropropene in bulk and with tetrafluoroethylene was studied at pressures between 5000 and 15000 atm and temperatures between 21 and 100°C. At 103 rad/hr the homopolymerization rates range from about 10-4 to 1%/hr. The activation enthalpy and volume are about 8 kcal/mole (33 kJ/mole) and -10 cm3/mole, respectively, for both isomers. The cis isomer polymerizes about twice as rapidly as the trans isomer. The latter freezes in the experimental range of temperature and pressure; the polymerization rate is very low in solid phase. Polymer intrinsic viscosities increase with polymerization pressure and decrease with polymerization temperature; the largest value obtained was 0.23 dl/g. In the copolymerizations all reactivity ratios favor incorporation of tetrafluoroethylene by factors of 6-16. The preference is stronger when the trans isomer is used.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 51
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1985-1994 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Series of progressively crosslinked polystyrene have been prepared by the reaction off linear polystyrene with p-di(chloromethyl)benzene in dichloroethylene solution with stannic chloride as catalyst. By using a DTA technique it has been shown that the glass transition temperature Tg increases with crosslinking very much faster than is accounted for purely by increase in molecular weight. This type of crosslink is only about half as effective in increasing Tg as are crosslinks introduced by copolymerization of styrene with divinylbenzene. Thermal analysis by use of the thermal volatilization analysis (TVA) technique shows that stability, as measured by the evolution of volatile products, decreases as crosslinking progresses, and thermal gravimetric analysis (TGA) confirms this.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 52
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2021-2030 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Low concentrations of bromine (0.008-0.06M) were used to initiate photopolymerization of MMA in bulk and in diluted (near bulk) systems, the diluents or solvents used being benzene, toluene, dioxane, tetrahydrofuran, carbon tetrachloride, chloroform, methylene chloride, and methanol. Polymerization in bulk follows usual free-radical kinetics. Inert solvents (benzene, toluene) as well as the other solvents used enhance the rate of polymerization MMA even when used in the range of catalytic concentrations (0.04-0.4M). An initiation mechanism involving solvent molecules appears to be predominant in diluted systems.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 53
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2057-2068 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C-NMR spectra of ethylene-propylene copolymers and their model compounds were measured at 15.1 MHz. Assignments of the signals were carried out by using the equation of Grant and Paul and also by comparing the spectra with those of squalane, hydrogenated natural rubber, polyethylene, and atactic polypropylene. The accuracy and the precision of intensity measurements, that is, the deviation from the theoretical values and the scatter of the measurements, respectively, were checked for the spectra of squalane and hydrogenated natural rubber and were shown to be at most 12% for each of the signals. On the basis of these results the mole fractions of the four types of the dyad sequences, that is, the propylene-propylene (head-to-tail and head-to-head), the ethylene-propylene, and the ethylene-ethylene sequences, were determined together with the average sequence lengths of both monomer units.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 54
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1553-1564 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of oxidation of dimethyl sulfoxide by tervalent manganese was investigated in sulfuric and perchloric acid media at 40-45°C. A mechanism involving prior complexation between reactants followed by a reversible electron-transfer step was shown to be consistent with the kinetics. The radical ion thus produced initiates polymerization of acrylonitrile, the termination being effected by the oxidant. Rates of polymerization vary directly as the sulfoxide concentration and are proportional to the square of the monomer concentration and being independent of the oxidant. Oxidation as well as polymerization is retarded by Mn(II). Average degrees of polymerization lend support to the proposed mechanism. Rate parameters have been evaluated in the two media, and their significance is discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 55
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1615-1629 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Linear polyacroleins prepared by anionic polymerization give the structural repeat units of the types \documentclass{article}\pagestyle{empty}\begin{document}$ \rlap{--}[{\rm CH}\left( {{\rm CHO}} \right)\hbox{--} {\rm CH}_{\rm 2} {\rm \rlap{--} ], \rlap{--} [CH}_{\rm 2} \hbox{--} {\rm CH}\left( {{\rm CHO}} \right)\rlap{--} ], $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ \rlap{--} [{\rm CH}\left( {{\rm CH}\hbox {\rm CH}_2 } \right)\hbox{\rm O\rlap{--} ]} $\end{document} without any cyclization. Analysis of these polymers by several methods reveal the nature and amount of each structural species, and an estimation of their distribution along the polymeric chain.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 56
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1645-1651 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of the chemical structure of the functional portion as well as the comonomer composition on the photochromic behavior of vinyl polymers containing mercury thiocarbazonate functional groups in the side chains were investigated. It was found that, for p-acrylamidophenyl mercuric thiocarbazonate polymers, the uses of β-naphthyl and strongly electron-releasing p-methoxyphenyl groups for the thiocarbazone residue provide absorption maxima shifted somewhat to longer wavelengths as compared with the use of unsubstituted phenyl groups, whereas the electron-withdrawing o-trifluoromethylphenyl group brings about much larger shifts towards shorter wavelengths, the o-trifluoromethylphenyl group and those groups capable of exerting steric hindrances such as β-naphthyl and o-methylphenyl groups causing slower light and dark reactions too. The increase of free volumes in the polymers by regulating the comonomer composition, i.e., the lowering of Tg, was found to improve photochromic responses strikingly.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 57
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1683-1690 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkaline hydrolysis of model carbamates, polyurethanes, and poly(urethane-ureas) has been investigated. The model carbamates were based upon phenyl, benzyl, and cyclohexyl isocyanates. The polyurethanes and poly(urethane-ureas) were prepared from tolylene diisocyanate (TDI), xylylene diisocyanate (XDI), and 4,4′-dicyclohexylmethane diisocyanate (H12MDI) and a poly(oxyethylene)glycol of 6000 molecular weight. Pseudo-first-order rate constants of hydrolysis were obtained in aqueous pyridine solution at 110°C, and second-order rate constants were obtained in aqueous KOH solution for the model biscarbamates. Pseudo-first-order rate constants of hydrolysis were obtained in alcoholic KOH solution for the polyurethanes and poly(urethane-ureas). The hydrolysis of the model carbamates showed that the stability increased in the following manner: phenyl 〈 benzyl 〈 cyclohexyl. The pseudo-first-order rate constants were dependent upon the pKb of the corresponding amines. The hydrolysis of the polyurethanes and poly(urethane-ureas) showed that the stability increased in the following manner: aromatic 〈 aralkyl 〈 cycloaliphatic. It was shown that polyurethanes are more susceptible to alkaline hydrolysis than to acidic hydrolysis.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 58
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1721-1732 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of cure of polybutadiene with molecular weights varying from 12,500 to 92,000 g/mole and containing 23-93% of 1,2 microstructure were investigated at two levels of dicumyl peroxide and two temperatures. The relative rates of termination were determined as a function of vinyl content and of reactive additives. Sol-gel measurements showed that molecular weights between crosslinks of less than 100 g/mole could be obtained. Network formation was found to be a polymerization process in which each free radical formed started only one crosslink chain. However, at high initiator levels chain scission did occur during cure.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 59
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1753-1755 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 60
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2547-2556 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of grafting reactions of styrene to preirradiated cellulose acetate have been studied by labeling the active sites with bromine atoms. The dilution of styrene monomer with methanol affected grafting reactions remarkedly: e.g., as the concentration of methanol in monomer solutions increased, the growth rates of individual graft radicals decreased while the average lifetimes increased. The integrated amounts of active sites which participated in grafting reactions were also affected by the constitution of monomer solutions and varied roughly in proportion to the extents of swelling of cellulose acetate. Grafting yields for styrene/methanol = 1/1 were higher than for 3/1 and 1/3 throughout the duration of grafting reactions, which is due not only to the high molecular weight of graft chains but also to the large number of graft chains for the 1/1 system compared to the other systems.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 61
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2601-2613 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Spectroscopic studies made on the bisphenol A polycarbonate-sulfur dioxide system showed evidence of interaction between polymer and penetrant. Equilibrium studies made on solutions of sulfur dioxide and organic carbonates chosen as monomer analogs showed that complexes of the donor-acceptor type were formed, and that at temperatures of 15°C and less the stoichiometry of these was greater than 1:1. The procedures described are compared with those used in other donor-acceptor studies, and the results observed from the equilibrium studies are interpreted by using data reported for other sulfur dioxide-donor systems.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 62
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methacrylaldehyde, methyl methacrylate, methacrylonitrile, styrene and isoprene readily polymerize on potassium-graphite inclusion compounds in ethereal and hydrocarbon solvents. The structure of polymethacrylaldehyde, poly(methyl methacrylate), and polyisoprene as well as the composition of styrene-acrylonitrile and styrene-isoprene copolymers have been investigated. The copolymers have a high content of styrene units which is interpreted in terms of selective adsorption of styrene on the initiator surface.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 63
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2623-2632 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New thermally stable poly(imide-oxoisoindolobenzothiadiazine dioxides) (PIOD) have been prepared by the three-step cyclopolycondensation reaction of diaminobenzenesulfonamides with aromatic tetracarboxylic dianhydrides. The polymerization proceeded through the formation of poly(amic acid-sulfonamides) (PAAS), followed by cyclodehydration to yield polyimide-sulfonamides (PIS), which were subsequently converted to PIOD at 300°C. PAAS having inherent viscosities in the range of 0.1-0.5 in N-methyl-2-pyrrolidone (NMP) were obtained in approximately quantitative yield. PIOD were insoluble in most organic solvents, whereas PAAS and PIS were soluble in NMP and dimethyl sulfoxide. Differential thermal analysis and thermogravimetric analysis indicated that PIOD began to decompose at 460°C in air. The cyclodehydration of the model compounds was also investigated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 64
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2633-2651 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Five series of two-component blend filaments, comprising nylon 6 (N6) and nylon 66 (N66), nylon 610 (N610), nylon 11 (N11), nylon 12 (N12), or poly(ethylene terephthalate) (PET), were prepared by using a research spinning machine and a conventional drawing machine. The microstructure and the physical properties of the resultant filaments were evaluated with a tensile tester, a optical microscope, a density-gradient column, and a DTA instrument. When both components were mixed homogeneously so that they would form a three-dimensional network, the tensile properties of the blend filament were at least equivalent to the values predicted from those of both components. On the other hand, as in the cases of 30/70 and 70/30 N6-PET, when the minor component was discretely distributed as short fibrils in the matrix of the major component, the blend filament had an extremely weak tenacity. A supertenacity filament was obtained from 50/50 N6-N610. The marked increase of the tensil strength and the initial modulus of 50/50 N6-N610, about 12 g/den and 520 kg/mm2, respectively, may be due to a significant increase in the crystallinity and the orientation of the blend.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 65
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2665-2680 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The study of chain-transfer reactions in thermal and AIBN-initiated polymerization of styrene is aimed at the determination of transfer constants to the solvents at 60°C. For thermal polymerization the transfer constants Cs to acetone, chloroform, and chloroform mixed with acetone are 3.2 × 10-5, 4.1 × 10-5, and 4.4 × 10-5, respectively. In the case of AIBN-initiated polymerization, the transfer constant of chloroform in the mixture acetone-chloroform is Cs = 3.3 × 10-4. All these transfer constants are average values. It has been found that neither acetone nor chloroform satisfies the Mayo equation in the presence of transfer agent very well. These anomalies can be explained by assuming a complexation phenomenon. The changes in the polarity and resonance are taken into account. It is considered that in the chain-transfer reactions under investigation, the association or complex-forming ability of solvent and monomer or polymer play a role. In studying the chain-transfer reaction in the acetone-chloroform solvent mixture another phenomenon affecting the determination of the chain transfer constant is assumed. This phenomenon consists in formation of associates in which both solvents participate.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 66
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2711-2712 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 67
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2691-2701 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cohesive films of a series of chromium(III) tris(phosphinates)[Cr(OPRR′O)(OPR″-R‴O)(OPR*R**O)]y in which the side groups on the phosphorus are alkyl, phenyl, and/or hydrogen groups have been prepared by reaction casting or by hot pressing. The preparative reaction appears to involve conversion of an aquahydroxo or hydroxo chromium(III) bis(phosphinate) to an intermediate hydroxo bis(phosphinate) containing coordinated phosphinic acid followed by an intrachain reaction leading to the tris(phosphinate). Tensile strengths of the chromium(III) tris(phosphinates) range from 100 to 5600 psi, elongations from less than 1 to 100%. Thermogravimetric data indicate that major decomposition occurs at temperatures from 200 to 435°C in air and from 410 to 510°C in nitrogen. Infrared spectra and physical properties are interpreted to support a structure for the chromium(III) tris(phosphinates) which is based on linear, triple-bridged chains. The presence of octyl or other long alkyl side groups on the phosphorus improves the physical properties, presumably by internal plasticization, but leads to decreased thermal stability.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 68
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2719-2725 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Density and x-ray diffraction measurements of the degree of crystallinity have been made on copolymers of polyamide 6 PA-6 with hexamethylenediamine terephthalate and ethylenediamine terephthalate ranging composition from 4 to 35 mole-% of the terephthalates. The degree of crystallinity can be determined from the ratio of the sum of mass contribution products of the crystalline regions for each of the comonomers to the total copolymer mass. Such a procedure can be used when the molar fractions of comonomers in copolymer are known. The results obtained are in agreement with the theoretical values.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 69
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2739-2751 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have investigated the effect of methanesulfonic acid (MSA) on the circular dichroism (CD) spectra of some stereoregular polyamides derived from three cyclic 1,2-dicarboxylic acids (I-III) and piperazine (PIP), trans-2,5-dimethylpiperazine (DMPIP), or N,N′-dimethylethylenediamine (DMED). On the basis of a detailed knowledge of the conformational properties of these polymers, we have attempted an essentially empirical interpretation of the CD spectra and of their relative changes. A striking dependence of the optical properties from the conformational properties and/or transitions in the polymers has been found. Although far from suggesting a 1:1 correspondence between CD spectra and conformational changes, we wish to stress their general correspondence.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 70
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2767-2776 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On exhaustive drying of sulfonated polystyrene-based ion-exchange resins, it is shown that free-radical centers develop. These have been examined by electron-spin resonance spectroscopy. The formation of the free radicals is largely reversible with respect to desorption and sorption of water which was measured by means of a quartz spiral microbalance. The spin-concentration isotherm as a function of sorbed water concentration is obtained. The presence of free radicals, dependent on water content in the resins, interferes with proton magnetic relaxation studies of hydration of ionized resins by providing a faster electron-spin coupled nuclear magnetic relaxation mechanism.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 71
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2793-2811 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(phenylene sulfides) were synthesized from m-benzenedithiol and aromatic dibromides in a basic medium of potassium carbonate in dimethylformamide or dimethylacetamide. The products obtained were slightly off-white with relatively low melting ranges and had inherent viscosities in the 0.2-0.4 dl/g range in hexamethylphosphoric triamide. Similar poly(phenylene sulfides) containing pendant cyano groups along the polymer chains were obtained by the use of 5 mole-% of either 2,4-dichlorobenzonitrile or 3,5-dichlorobenzonitrile. The products were similar to the pure polyphenylene sulfides, except that they showed lower melting ranges and gave insoluble products when heated alone or in the presence of zinc chloride.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 72
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2257-2263 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radiation-induced solid-state polymerization of cyclohexene sulfide has been investigated. Differential thermal analysis shows that this compound has a phase transition point at -74°C and behaves as a plastic crystal in the temperature range from -74 to -20°C (melting point). By rapid cooling, this plastic crystal was easily supercooled, and below -166°C a glassy crystal, i.e., a supercooled nonequilibrium state of plastic crystal, was obtained. In-source polymerization proceeded in the plastic crystalline state. Postpolymerization of glassy crystalline monomer irradiated at -196°C occurred above -166°C (glass transition point) during subsequent heating.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 73
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2273-2285 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cis-trans photoisomerization reaction of 1,4-polybutadiene was carried out below the melting points on films of polymers containing high trans-1,4 contents. Under the proper conditions of temperature and polymer composition, the reaction was observed to undergo an anti-equilibrium behavior, which was attributed to an irreversible crystallization of repeating units after isomerization from cis to trans structure. As a result, the trans composition passed through a minimum with reaction time while crystallinity increased throughout the reaction, and unexpectedly the β crystalline form was observed well below the α-β transition temperature. The composition-time behavior observed was rationalized on the basis of incorporation of trans units into crystalline regions on the lamellar fold surfaces and discussed within the framework of the proposed requirements for crystallization-induced reactions of copolymers.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 74
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2295-2304 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oligomer of polyisoprenyllithium, 2,5,5-trimethylhexen-2-yllithium, formed from tert-butyllithium and one molecule of isoprene in benzene has a structure similar to that of higher members of the series and also similar properties. In THF only one stereoisomer is stable, and an attempt is made to determine its stereostructure. The lithium compound was converted at low temperature to the acid, and this by a series of steps in which the structure was monitored to the acid's parent hydrocarbon 3,6,6-trimethyl-3-heptene. This was then compared with a synthesized sample of this hydrocarbon of known structure. In this way it was shown that the original lithium compound had a cis configuration in tetrahydrofuran solution.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 75
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2315-2327 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methacryloyl-L-valine methyl ester (MAVM) and maleic anhydride (MAn) were photopolymerized without initiator in dioxane at 35°C. Copolymer having a 1:1 molar ratio of the monomers was obtained regardless of both molar ratio of monomers in the feed and polymerization time. The circular dichroism (CD) spectrum of the copolymer before and after hydrolysis showed the induction of asymmetric centers into the polymer main chain. Spectroscopic and kinetic studies suggested the alternating and stereoregular copolymerization of MAVM and MAn, in which a charge transfer complex with a 1:1 molar ratio of monomers participated.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 76
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2343-2355 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal degradation of two β-chlorinated versions of poly(isopropylidene carboxylate) has been studied by the combined thermogravimetric and gas evolution techniques described previously. Poly(3-chloro-2-methyl-2-hydroxypropionic acid) was found to decompose by a predominantly first-order process which was characterized by kinetic parameters similar to those obtained for poly(isopropylidene carboxylate). These are interpreted in terms of an intramolecular ester-exchange process. As the reaction proceeds intermolecular elimination of hydrogen chloride leads to crosslinking and ultimately to the formation of a carbonaceous char. This process is much more marked in the randomly β-chlorinated analog of poly(isopropylidene carboxylate). With this polymer, drastic deviation from first-order behavior is observed in thermogravimetric results, even in the early stages of reaction. Gas evolution analysis, being more influenced by degradation fragments having an appreciable vapor pressure, yields reasonable first-order data and indicates that the intramolecular interchange mechanism is still an important process. In general, the introduction of β-chlorine atoms is seen to reduce the rate of thermal decomposition of poly-α-esters.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 77
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the cyclocopolymerizations of diallyl phthalate (DAP) with monovinyl monomers the reactivity ratio of the cyclized radical, rc, was smaller than that of the uncyclized radical, r1; this was ascribed to steric hindrance in the addition reaction of the cyclized radical with DAP. In this paper, the validity of the values of rc and r1 is discussed on the basis of model experiments, i.e., the copolymerization of DAP in dilute solution corresponding to rc and that of allyl propyl phthalate, to r1. The copolymerizations of methyl allyl phthalate and allyl octyl phthalate with vinyl acetate are also presented.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 78
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2377-2381 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 79
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2975-2989 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methyl methacrylate (MMA) was polymerized by radical initiation at 25°C or 35°C in various solvents in the presence of stereoregular poly(methyl methacrylate) (PMMA). The occurrence of stereospecific replica polymerization appeared to be related to the capability of stereoassociation of isotactic and syndiotactic PMMA. The solvents can be roughly divided into three types. Type A solvents are polar solvents, which promote stereoassociation resulting in gelation and precipitation. Examples are dimethylformamide, dimethyl sulfoxide, and acetone. Type B solvents are nonpolar aromatic solvents like benzene and toluene, wherein stereoassociation is weaker but still leads to gelation. Type C solvents are very good solvents, in which stereoassociation does not occur. Chloroform and dichloromethane belong to this class. In solvents of type A as well as type B, polymerization in the presence of i-PMMA as a polymer matrix was syndiospecific. However, in the presence of s-PMMA as a polymer matrix the polymerization was isospecific only in type A solvents. The syndiotactic or isotactic triad contents of the polymer formed could be as high as ca. 90% at low conversions. In solvents of type C, polymerization in the presence of stereoregular PMMA proceeds according to a normal radical mechanism. Syndiotacticity was always less than 70%. Stereocomplexes formed in situ during replica polymerization were partly crystalline as detected by x-ray diffraction. The highest crystallinity was detected in those formed in type A solvents.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 80
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 3017-3020 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An expression is derived for the partitioning of a solute molecule in a two-phase system: swollen gel and free solvent. The approach is thermodynamic, and no specific mechanism for the accessibility of the solute to the gel is assumed. Instead, general interaction terms between the components, i.e., polymer-solvent-solute, are introduced.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 81
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2463-2487 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical copolymerization of butyl methacrylate with 2,3-dimethylbutadiene in the presence of Al(C2H5)2Cl or ZnCl2 results in alternating copolymers. The nature of active centers and the mechanism of polymerization in these systems have been studied by means of ESR measurements in combination with calorimetry at low temperatures. The active centers are monoradicals propagating by alternative addition of single monomer molecules; thus the reaction can be described in terms of a conventional kinetic scheme of radical additional polymerization. Participation of binary donor - acceptor complexes of the monomers in the reaction has not been confirmed. Similar conclusions have been drawn for the other alternating system studied, maleic anhydride-2,3-dimethylbutadiene. The feasibility of formation of alternating copolymers in the studied systems by the conventional mechanism of binary radical copolymerization has been confirmed by qualitative quantum-chemical treatment of the propagation reactions with due account to the donor-acceptor interactions in the transition state.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 82
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2569-2590 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study has been conducted of the relative reactivity of a series of dienes (butadiene, isoprene, 2,3-dimethylbutadiene, cyclohexadiene-1,3), as well as of butadiene and styrene, in copolymerization by various coordination catalyst systems based on transition metals: nickel, cobalt, titanium, chromium, molybdenum, and tungsten. The microstructure of homopolymers and copolymers of dienes has been investigated. Regularities have been established in the mutual influence of the comonomers on the microstructure of a polymer chain. Experimental data on the influence of the concentration of diene monomer, and electron-donating and electron-accepting compounds on the microstructure of polydiene chain have been used in discussing the alternative mechanisms of stereoregulation in diene polymerization by active centers of the π-allyl type.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 83
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2591-2600 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of γ-radiation on aqueous polystyrene emulsions were followed by measurements by intrinsic viscosities of soluble polymer in toluene. Estimates of incipient gel dose from intrinsic viscosity data do not coincide closely with those from measurements of gel content. This uncertainty and those in molecular weight averages make it difficult to assign a precise value to G(crosslink), even when the scission crosslinking ratio in the particular system is reliably known. The intrinsic viscosity of sol polymer in the postgel region decreases with increasing dose to an asymptotic value. The decrease is as expected if larger molecules are progressively linked into the gel network and the asymptote may be attributable to cyclization. Present theories of branching do not seem to be applicable for quantitative estimation of scission/crosslinking ratios caused by irradiation of polystyrene. This is probably connected with deficiencies in the theoretical connection between radius of gyration and intrinsic viscosity in good solvents. Diallyl fumarate and diallyl maleate increased crosslinking rates, but only at low doses. Chain scission was enhanced by addition of 1,2-dichloroethylene and 2,5-dimethylhexane-2,5-dihydroperoxide.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 84
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of vinyl chloride polymerization by titanium tetrabutoxide-ethylaluminum sesquichloride catalyst system was investigated from the view of the stereoregularity of poly(vinyl chloride). The samples were prepared at a selected temperature in the range from 23 to -78°C. The tactic triads, obtained from 220-MHz NMR spectra, show clearly the adequacy of Bernoullian statistics in describing the mechanism for stereochemical propagation. The chain propagation proceeds according to Bernoullian statistics with syndiotactic placements favored by 550 cal/mole. These results suggest that vinyl chloride polymerizes by a free-radical mechanism under the action of the present catalyst system.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 85
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2681-2690 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced copolymerization of isobutyl vinyl ether with trichloroethylene was investigated in the temperature range from -50°C to 100°C over a wide range of comonomer compositions. A copolymer was obtained in which the monomers alternate with regularity along the polymer chain over essentially the entire range of comonomer compositions. Both the rate of copolymerization and the number-average molecular weight of the resulting copolymer were found to depend strongly on the initial comonomer composition. The monomer reactivity ratios were determined and correspond well with calculated values. An apparent activation energy of 3.2 kcal/mole was obtained for the copolymerization process which exhibits a dose rate dependence of 0.72. The number-average molecular weight was found to be strongly dependent on the irradiation temperature, reaching a maximum value at 5°C.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 86
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2703-2708 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 87
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2709-2710 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 88
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2713-2717 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 89
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2727-2737 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational equilibria of piperidine diamides derived from five cyclic 1,2-dicarboxylic acids (I-V) have been investigated by dipole moment measurements and a priori conformational energy estimates. Since these diamides represent the building blocks of the polyamides derived from the above cyclic diacids and piperazine or trans-2,5-dimethylpiperazine, the results obtained in the study of the models have been used to investigate the conformation of the polymers. The overall evidence suggests that cyclopentane, cyclohexane, and bicyclooctane piperazine polymers behave as rigid rods in which the structural units possess approximately the same conformational preference exhibited by the respective model diamides.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 90
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2753-2765 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The monomer h6-(2-phenylethyl Acrylate) tricarbonylchromium (PEAC) was synthesized and copolymerized in solution at 70°C with styrene, methyl acrylate, acrylonitrile, and 2-phenylethyl acrylate, azobisisobutyronitrile being used as the initiator. In ethyl acetate solvent the relative reactivity ratios were crudely approximated. The copolymers all exhibited binodal molecular weight distributions, the high molecular weight node probably resulting from branching. The h6-benzenetricarbonylchromium unit decomposed when exposed to sunlight or ultraviolet light both in air and under N2. In air, Cr2O3 was initially formed within copolymer films. Several unsuccessful attempts were made to prepare h6-(2-phenylethyl acrylate)tricarbonylmolybdenum, (III), the molybdenum analog of PEAC, from arenes and both Mo(CO)6 and (CH3CN)3Mo(CO)3. These reactions are described.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 91
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Lithium diethylamide has been found to be an active initiator for the polymerization of isoprene both in hydrocarbon media and in a variety of polar solvents, such as diethyl ether and tetrahydrofuran. The successful initiation of styrene polymerization is, however, strongly dependent upon the type of solvent employed. Thus no polymerization is observed in hydrocarbon media or in diethyl ether solution, but polymerization occurs rapidly in either tetrahydrofuran or 1,2-dimethoxyethane solution. These polymerization processes are anionic in nature and are characterized by sigmoidal conversion-time plots, indicating that the initiation reactions are relatively slow compared to chain propagation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 92
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2813-2845 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Efficiencies of polymer radical production by thermal decomposition of di-tert-butylperoxy oxalate (DBPO) have been measured in bulk atactic polypropylene (PP) at 25-55°C; they range from 1 to 26%, depending on [DBPO], temperature, and presence of oxygen. Most of the polymer radicals thus produced disproportionate in the absence of oxygen but form peroxy radicals in its presence. Most of the pairs of peroxy radicals interact by a first-order reaction in the polymer cage. The fraction that escapes gives hydroperoxide in a reaction that is half order in rate of initiation. In interactions of polymer peroxy radicals, in or out of the cage, about one-third give dialkyl peroxides and immediate chain termination, two-thirds give alkoxy radicals. About one-third of the later cleave at 45°C; the rest abstract hydrogen to give hydroxy groups and new polymer and polymer peroxy radicals. The primary peroxy radicals from cleavage account for the rest of the chain termination. Cleavage of alkoxy radicals and crosslinking of PP through dialkyl peroxides nearly compensate. Up to 70% of the oxygen absorbed has been found in hydroperoxides. The formation of these can be completely inhibited, but cage reactions are unaffected by inhibitors. Concentrations of free polymer peroxy radicals have been measured by electron spin resonance and found to be very high, about 10-3M at 58-63°C. Comparison with results on 2,4-dimethylpentane indicate that rate constants for both chain propagation and termination in the polymer are much smaller than those for the model hydrocarbon but that the ratio, kp/(2kt)½, is about the same.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 93
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2899-2907 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: There appear to be no unusual effects of phase change or near-ultraviolet radiation on the reactions of alkoxy radical models for atactic polypropylene. The oxidation of purified atactic polypropylene by singlet oxygen is not an important process at 50°. Photochemical and thermal cleavages of tert-amyloxy radicals, a model for polypropylene oxy radicals, give nearly the same ratio of ka/kd at 50°C. Photochemical cleavage of the model compound 1,1-dinonylethyl hydroperoxide (10-methyl-10-nonadecyl hydropenoxide) gives exclusive cleavage of a nonyl group both in solution and in polypropylene film at 50°C.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 94
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2947-2960 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of alkyl acyl cyanides with electron-rich aromatic substrates in highly acidic media was found to give high yields of bisadducts. Reactions with phenol produced two new eyanobisphenols which readily underwent polycondensation with acid chlorides. The resultant polyesters can be directly compared to the polyesters of bisphenol-A (BPA) strictly on the basis of polar effects since steric differences are nominal. Thermal, mechanical, electrical and solubility characteristics are reported for the cyanopolycarbonates, which show higher thermal transitions and thermal stability than BPA polycarbonate.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 95
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochemical reactions of N-vinylcarbazole (VCZ), studied in various solvents, were profoundly influenced by the atmosphere. In the deaerated system radical polymerization of VCZ occurred in various solvents, e.g., tetrahydrofuran, acetone, ethyl methyl ketone, acetonitrile, methanol, sulfolane, N,N-dimethylformamide (DMF), or dimethyl sulfoxide (DMSO). By contrast, when dissolved oxygen was present, cyclodimerization of VCZ occurred exclusively to give trans-1,2-dicarbazole-9-yl-cyclobutane in such polar, basic solvents as acetone, ethyl methyl ketone, acetonitrile or methanol. In stronger basic solvents, i.e., sulfolane, DMF, or DMSO, simultaneous radical polymerization and cyclodimerization of VCZ proceeded, the ratio of the cyclodimerization to the radical polymerization decreasing in the order, sulfolane 〉 DMF 〉 DMSO. In dichloromethane, on the other hand, cationic polymerization of VCZ occurred irrespective of the atmosphere. It is suggested that oxygen acts as an electron acceptor to the excited VCZ, electron transfer occurring in polar solvents from the excited VCZ to oxygen to give transient VCZ cation radical. The effect of solvent basicity on the photocyclodimerization of VCZ is discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 96
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 105-120 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radiation-induced emulsion polymerization of ethylene with ammonium perfluoro-octanoate as an emulsifier was studied in order to elucidate the effect of the number of polymer particles. Owing to the stable structure of the emulsifier from a radical attack, no C—F bond was detected in the polyethylene as expected. The polyethylene produced was mostly gel containing a small amount of low molecular weight polyethylene. This may be attributable to chain transfer to the polyethylene. The effects of dose rate and of concentration of the emulsifier were determined without considering the chain-transfer reaction to the emulsifier. By considering the escape of the radical which is produced by chain transfer to the monomer from the polymer particle to the aqueous phase at the steady state, the following equation is derived: \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{{R_p }}{I} = \frac{{K_i K_p ^2 [{\rm N}_{\rm T} ]}}{{2K_0 \alpha R_p }} - \frac{{K_i K_p }}{{K_{0\alpha } }} $$\end{document} The experimental results could be explained by this equation, and the apparent rate constants were obtained.
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 97
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 183-189 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Anionic polymerization of phenyl vinyl ketone (PVK) was carried out in toluene at 0°C by use of an initiator, ethylzinc 1,3-diphenyl-1-pentene-1-olate (I), which possesses the same structure as the growing chain end of PVK in the diethylzinc (ZnEt2)-initiated polymerization. A unimodal molecular weight distribution was found in the obtained polymer. The polymerization system exhibited a “living characteristic” with the initiator efficiency being 1.0.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 98
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 167-181 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of a Mannich base type-polyamine polymer with iodine (I2) was studied kinetically and thermodynamically in order to clarify the polymer effects in the formation of triiodide ions (I3-). N,N-Dimethyl-p-(4-methylpiperazinomethyl) aniline and 1,4-dimethylpiperazine were used as low molecular weight donor model compounds. Triiodide ions are produced from the polyamine-I2 system immediately after mixing the two-component solutions, while in the systems with I2 and N,N-dimethyl-p-(4-methyl-piperazinomethyl)aniline and 1,4-dimethylpiperazine they are obtained only when relatively high concentrations of both donor and acceptor solutions were mixed. This is explained by the entropic contributions of the polymer chain such as the stacking effect of donor nitrogen atoms, i.e., the increment of local donor concentration around I2 in the reaction field. The relation between the solution behavior of the reaction systems and the rate of formation of I3- ions also supports this kind of polymer effect. The effects of neighboring groups and dielectric constant on the reaction are also discussed.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 99
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 201-210 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to examine effect of the carbonyl group in carbon monoxide-vinyl chloride copolymer, poly(CO-VC), photoirradiation with a high-pressure mercury lamp on the copolymer was carried out. Poly(CO-VC) had a rate of dehydrochlorination three times that of PVC, and the reaction involved a decrease in chlorine content. Also there was a marked change in the ultraviolet spectra of the photoirradiated films. However, no pronounced change of molecular weight was observed, but a change in Rf in TLC was observed clearly. These facts confirmed that photoirradiation of poly(CO-VC) produced a structural change by dehydrochlorination without serious decrease of molecular weight. In addition, photodehydrochlorination of the copolymer or PVC film was followed kinetically, and after ozonolysis of the dehydrochlorinated polymers, the number-average molecular weights were measured. From the results of degree of dehydrochlorination and molecular weight, the number average of conjugated double bonds or carbonyl groups was estimated. A mechanism for dehydrochlorination process by photo-irradiation is suggested.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 100
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 241-246 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...