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  • Wiley-Blackwell  (6)
  • Blackwell Publishing Ltd  (4)
  • American Chemical Society (ACS)
  • Oxford University Press
  • 2000-2004
  • 1965-1969  (10)
  • 1966  (10)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Review of income and wealth 12 (1966), S. 0 
    ISSN: 1475-4991
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Economics
    Notes: After an introduction setting out the general state of work on the national accounts in the Middle East the author considers the principal uses of national accounts statistics in less developed countries. The first group of uses discussed is in connexion with the measurement of growth and the making of international comparisons. The author is of the opinion that in many cases the primary statistical series are so weak that the fact they they are combined together into a series called national income or gross domestic product lends to them a significance which they do not really possess. The real problem is to improve the quality of the primary series.A second use of national accounts statistics is in connexion with fiscal and budgetary policy. In the statistically advanced countries this is one of the most important uses but in the less developed countries budgetary policy has not yet reached a level of sophistication which would call for the use of national accounts data. Moreover, the time factor involved in assembling accurate national accounts estimates militates against their effective use for short term forecasting.The author considers that the most important use for national accounts statistics is to provide a framework for development planning. The United Nations system is not altogether appropriate for this purpose. It grew up primarily as a system for recording income flows but in development planning one is concerned equally with commodity flows with a great deal of attention being focussed upon intermediate products. The proposals of the working group of African Statisticians for an adaptation of the S.N.A. to African countries represents a most important advance in this respect.In the final section of the paper the author advocates a broader definition of capital formation to include developmental expenditure which is not properly defined as fixed capital formation. Education expenditure is cited as an example. It is suggested that in the national accounts it would be desirable to operate with gross concepts. However, the growth of the capital stock is obviously important in less developed countries and it is suggested that statistical techniques be devised to measure it directly wherever possible. Finally, attention is drawn to the ambiguities and weaknesses in the concept of residence as used at present in the S.N.A.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 129 (1966), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 129 (1966), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 78 (1966), S. 609-609 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1617-1623 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The n-alkyl α-cyanoacrylates from methyl through n-octyl exhibit a reverse order of polymerization rate on biological substrates compared to that on water. On water, the lower homologs spread and polymerize rapidly, whereas the higher homologs spread but polymerize slowly. On biological substrates, the lower homologs do not spread or spread slightly and the higher homologs exhibit large spreadabilities and very rapid polymerization rates. Determination of the spreading coefficients for these systems by using the monomers or model compounds confirm the observed spreadabilities. It is proposed that the increased rate of polymerization of the higher homologs on biological substrates may be due to increased catalyst concentrations on these surfaces or to the solubilization of the higher homologs at the interface, making the catalyst sites more available to the monomer. The suggestion is made that if the liquid monomers spread and orient on the substrate and subsequently polymerize, the polymers will maintain the orientation. If such is the case, a technique is available for preparing stereospecific vinyl polymers which may have different spatial configurations depending on the polarity of the liquid substrate upon which they have been allowed to spread and polymerize.
    Additional Material: 1 Ill.
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  • 7
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Subunits of immunoglobulins have been prepared by two methods, both of which have contributed to our knowledge of the structural basis of antibody specificity. The first method is enzymic hydrolysis with either papain or pepsin and leads to the unequivocal conclusion that each combining site is contained in a fragment (Fab) of about 45,000 molecular weight and formed from the light chain and the N-terminal half of the heavy chain, the Fd fragment. The second method of preparing subunits is to reduce the interchain disulfide bonds and to isolate the chains. This should decide whether the combining site is in the Fd fragment, the light chain, or is formed jointly by both. In fact, considerable loss of affinity for the antigen follows, whatever technique is used to dissociate the peptide chains and, although many papers have been published on this subject, no definite answer has yet been obtained. Although the majority opinion probably favors the view that both chains are concerned in the formation of the combining site, our tentative conclusion is that the site is placed entirely in the heavy chain and that the light chain has only a semispecific role in facilitating the reformation of the native configuration of the heavy chain after its disruption under the conditions necessary for dissociation of the two chains.
    Additional Material: 5 Ill.
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  • 8
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Fraktionierung von Polymeren durch Gradientenelution beruht auf der Abnahme der Löslichkeit mit zunehmendem Molekulargewicht. Diesem Prozeß kann sich jedoch ein Einfluß der Taktizität überlagern. In der vorliegenden Arbeit wird dies für den Fall der Fraktionierung von Polypropylen untersucht. Hierzu werden typische “ataktische” und “isotaktische” Fraktionen verwendet, die sich durch ihre Löslichkeit in n-Heptan unterscheiden. Der Taktizitätsgrad wird an Hand hochaufgelöster PMR-Spektren der Methylenprotonen ermittelt. Eine Eichkurve wird mitgeteilt, die auf Ergebnissen dieser Arbeit und auf Messungen von SATOH und KATO beruht. Die Beziehung wird mit den Spektren aus den Veröffentlichungen von STEHLING und von WOODREY verglichen. Änderungen der Taktizität mit dem Molekulargewicht sind bei den Fraktionen mit niedrigen Molekulargewichten am ausgeprägtesten, und zwar sowohl bei “ataktischen” als auch bei “isotaktischen” Polypropylenen. Die Auswirkung dieser Tatsache auf die scheinbare Molekulargewichtsverteilung wird diskutiert.
    Notes: The basis for gradient-elution fractionation is a regular decrease in solubility with an increase in polymer molecular weight. tacticity, however, can be an overlapping effect in the solvent separation process. In this study, the effect of tacticity in the fractionation of polypropylene has been studied using representative “atactic” and “isotactic” polymers, defined by heptane solubility. Typical and published column techniques have been used. A high resolution proton magnetic resonance analysis of protons in the chain methylene region was used for evaluation of tactic placement. A new tacticity correlation was developed which is based on data obtained here and on PMR results on polypropylene reported by SATOH and KATO. This correlation has been compared to published spectra of STEHLING and of WOODBREY. Changes of tacticity with molecular weight are most prominently observed in the first gradient-elution fractions from both “atactic” and “isotactic” polypropylenes. The implication of these results concerning apparent molecular weights and distributions is discussed.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 4 (1966), S. 707-711 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 189-195 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A high-resolution proton magnetic resonance compositional analysis has been developed for propylene polymers containing 0-40 wt.-% ethylene as either homopolymer or copolymer blocks. The test is independent of tacticity and provides qualitative information on copolymer sequencing and propylene chain structure. The analysis was developed using a series of standard reference polymers synthesized to contain various ratios of C14-tagged ethylene and propylene. The compositional standards were established by radiotracer analysis for C14 and by preparing weighed physical mixtures of homopolymers. Spectra were obtained at 200 ± 10°C. by placing externally heated polymer solutions into a conventional probe of a Varian A-60 proton spectrometer. All measurements were made on ± 10% polymer solutions in diphenyl ether. Analyses are accurate to about ± 10% at higher ethylene concentrations. The method is sensitive, with less precision, to below 1% for ethylene either as blocks or homopolymer.
    Additional Material: 2 Ill.
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