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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 24 (1991), S. 5278-5282 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 20 (1988), S. 253-260 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary New UV-curable solventless flexible transparent coatings have been prepared of acrylate- and methacrylate-capped linear or three-arm star polyisobutylenes PIB in the presence of conventional “reactive diluents” (multifunctional acrylate or methacrylate esters) and a UV-sensitizer. Solvent extraction studies show essentially complete network formation. The swelling ratios were surprisingly small indicating highly crosslinked gels. Films cast on glass, Teflon, stainless steel and aluminum and UV cured very strongly adhere to these surfaces and could not be removed without destroying the films. Films obtained by casting on aluminum, UV curing and subsequently dissolving the support by concentrated NaOH, contain no pinholes. DSC traces show a low and a high temperature transition characteristic of a domain separated morphology of soft PIB and hard acrylate or methacrylate segments. The exact positions of the transitions in the range from −57 to −45°C, and from 62 to 78°C are affected by the overall film composition. Tensile and elongation data have been obtained. The water absorption of these highly hydrophobic coatings is negligible.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 20 (1988), S. 413-419 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Preparatory to a detailed presentation of a large body of accumulated information, representative data have been selected to demonstrate that well-defined narrow molecular weight distribution (MWD) (¯Mw/¯Mn ≅= 1.1) polyisobutylene (PIB) can be readily prepared in the Mn = 1000 – 100,000 range in the presence of certain types of electron pair donors (EDs) under a great variety of conditions. Specifically, many initiating systems, such as dicumyl chloride/BCl3, dicumyl alcohol/BCl3, 2-chloro-2,4,4-trimethylpentane/TiCl4, that induce nonliving polymerizations and/or give relatively broad MWD PIBs, in the presence of suitable EDs, e.g., dimethyl sulfoxide (DMSO), dimethyl acetamide (DMA), give rise to living polymerizations and yield narrow MWD products. Evidently, by the use of select EDs various undesirable side reactions, i.e., uncontrolled initiation, chain transfer, irreversible termination, indanyl end-group formation, etc., that plague carbocationic polymerizations and which therefore yield ill-defined relatively broad MWD products, can be eliminated and well-defined narrow MWD products can be obtained. The addition of EDs to otherwise extremely rapid carbocationic polymerizations results in lower controlled rates. All these observations and beneficial effects can be explained by controlled carbocation stabilization by EDs, a subject that will be explored and discussed in detail in this series of publications.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 22 (1989), S. 463-470 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Tert-alcohols in conjunction with BCl3 plus strong electron pair donors (EDs), such as dimethyl sulfoxide (DMSO) and dimethyl acetamide (DMA), have been found efficiently to initiate the living polymerization of isobutylene (IB) in methyl chloride diluent yielding narrow molecular weight distribution (MWD) polyisobutylenes (PIBs). For example, the aliphatic diol 2, 6-dihydroxy-2,4,4,6-tetramethylheptane/BCl3/ IB/DMA/−45°C system yields lineartert-chlorine telechelic $$\underset{\raise0.3em\hbox{$\smash{\scriptscriptstyle-}$}}{t} Cl - PIB - Cl\underset{\raise0.3em\hbox{$\smash{\scriptscriptstyle-}$}}{t} s$$ with Mw/Mn = 1.12 at Mn = 2500, and the aromatic triol 1,3,5-tri (2-hydroxyisopropyl)benzene/BCl3/IB/DMA/−50°C system produces three-arm startert-chlorine telechelic $$\begin{gathered} \underset{\raise0.3em\hbox{$\smash{\scriptscriptstyle-}$}}{t} Cl - \mathop {PIB}\limits_| - Cl\underset{\raise0.3em\hbox{$\smash{\scriptscriptstyle-}$}}{t} \hfill \\ Cl\underset{\raise0.3em\hbox{$\smash{\scriptscriptstyle-}$}}{t} \hfill \\ \end{gathered} $$ with Mw/Mn = 1.15 at Mn = 2000. Premixing experiments suggest that in the presence of excess BCl3 thetert-alcohols are rapidly transformed totert-chlorides, and that the latters are the true initiating species. Due to reversible termination the products are capped bytert-chlorines.
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  • 7
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract. The in-situ monitoring of the living carbocationic polymerization of isobutylene (IB) and styrene (St) with a fiber optic Attenuated Total Reflection (ATR) probe in the mid-IR "fingerprint" range is reported here for the first time. Monomer consumption was followed by the disappearance of the C=C stretching for both IB and St, and the C−H bending of the CH3-group in IB. The formation of polyisobutylene (PIB) was also monitored by tracing the asymmetrical doublet characteristic of C−H bending of the t-butyl groups of the PIB. Conversion measurements by conventional off-line gravimetry correlated well with the new technique.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 39 (1990), S. 119-144 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: New thermoplastic elastomers (TPEs) consisting of a central rubbery polyisobutylene (PIB) and glassy outer cyclopolyisoprene (cy-PIP) segments have been prepared by living carbocationic polymerization by sequential monomer addition. First the homopolymerization of isobutylene (IB) and isoprene (IP) have been investigated. The living polymerization of isobutylene initiated by the p-dicumyl methoxy (p-DiCumOMe)/TiCl4 system in CH3Cl/n-C6H14 mixtures at -80°C gave living ⊕PIB⊕ dications of desired molecular weights. The polymerization of IP induced by cumyl acetate (CumOAc)/TiCl4 or cumyl methyl ether (CumOMe)/TiCl4 systems in the same solvent at -40°C readily yielded gel-free off-white powders comprising trans-1,4-PIP units and cy-PIP sequences. The polymerization most likely proceeds by trans-1,4-PIP ⊕ cations that undergo inter/intramolecular alkylation and cyclization leading to branched multiblocks. Block copolymers were synthesized by the addition of IP to charges containing ⊕PIB⊕ dications of different molecular weights. Under select conditions pure (tr-1,4-PIP)-b-PIB-b-(tr-1,4-PIP) triblocks with relatively short tr-1,4-PIP sequences have been obtained. Extended reaction times result in multiblocks; most likely ⊕ (tr-1,4-PIP)-b-PIB-b-(tr-1,4-PIP) ⊕ dications induce alkylation and cyclization of PIP sequences. The extent of alkylation can be regulated by the viscosity of the medium (molecular weight and/or concentration of the PIB midblock). The rate of IP incorporation decelerates after an initial fast polymerization; however, it can be accelerated by adding fresh Lewis acid to the system. Although tr-1,4-PIP endblocks of linear triblocks can be completely cyclized by acid treatment to saturated products, multiblocks cannot, probably because of their branched structure. Transmission electron microscopy of multiblocks shows phase separation with PIB (95-70 mol%) the continuous phase (Tg = -73°C) and cy-PIP blocks (5-30 mol %) the discrete phase. The Tg of the cy-PIP domain is in the range 95-190°C and it is affected by the extent of cyclization and/or the length of the cy-PIP sequence. The new multiblock TPEs are soluble in organic solvents and can be melt-processed above ∼ 140°C. A multiblock TPE film containing 15 mol % glassy cy-PIP block and 85 mol % rubbery PIB block of M̄n = 55,500 cast from CCl4 exhibited to MPa tensile strength [120 MPa engineering strength (sigma true)] and 1200% elongation. The completely cyclized linear triblock shows higher Tg (≡ 180°C) but, due to its low cy-PIP content, exhibits unsatisfactory tensile properties.
    Additional Material: 14 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 85-92 
    ISSN: 0887-624X
    Keywords: multiarm-star ; polyisobutylene ; living polymerization ; macroinitiator ; 4-(1-hydroxy-1-methylethyl)styrene-co-styrene ; Core first method ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This article describes the synthesis of high molecular weight multiarm-star branched polyisobutylenes by living polymerization, using multifunctional initiators, and their initial characterization. First, macrointiators carrying tert-hydroxy function-alities were synthesized by the radical copolymerization of 4-(1-hydroxy-1-methylethyl)-styrene with styrene. This copolymerization system was found to be ideal with r1 ≡ r2 ≡ 1. Selected macroinitiators with average functionalities of 8-73 were then used to synthesize the star-branched polyisobutylenes. Polymers with molecular weights up to M̄n = 400,000 were obtained within 30-60-min reaction times, while under similar conditions the monofunctional 2-chloro-2,4,4-trimethylpentane initiator yielded M̄n ≈ 10,000 in 20 min. This can be viewed as an indirect proof that simultaneous multiple initiation took place with the macroinitiators. Under controlled conditions a branchedpolyisobutylene with M̄n = 375,000 and MWD = 1.2, and theoretically calculated 23 arms, with no detectable side products was obtained under living conditions in 60 min; the molecular weight of this polymer increased linearly with time. The branched structure of the polymers were demonstrated by SEC-LLS analysis and core destruction of selected samples. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 85-92, 1998
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Theory and Simulations 2 (1993), S. 141-149 
    ISSN: 1018-5054
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equations for the calculation of the degree of polymerization in 'modified' living polymerizations (living polymerizations in the presence of deliberately added terminating and transfer agents) are developed from a mechanistic/kinetic model. It is shown that a modifier, acting by the mechanism discussed, would cause more chain transfer in a continuous stirred tank reactor (CSTR) than in a batch. This is found to be the case in the living polymerization of 1,3-butadiene initiated by butyllithium in nonpolar solvents, such as cyclohexane, when 1,2-butadiene was used as a modifier. Under similar conditions no chain transfer was detected in batch polymerizations, while ≈ 20% transfer was found in a CSTR. The equations developed can be used to calculate the ratio of the rates of propagation and termination, kp/kt. CSTR data yielded kp/kt ≈ 480 at 90°C; re-evaluation of batch data published earlier by Adams et al. for the same system in hexane solvent yields kp/kt ≈ 1250 and 670 at 50° C and 70°C, respectively.
    Additional Material: 1 Ill.
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