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  • Wiley  (3)
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  • Wiley  (3)
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  • 1
    Online Resource
    Online Resource
    Wiley ; 2012
    In:  Scandinavian Journal of Statistics Vol. 39, No. 3 ( 2012-09), p. 543-553
    In: Scandinavian Journal of Statistics, Wiley, Vol. 39, No. 3 ( 2012-09), p. 543-553
    Type of Medium: Online Resource
    ISSN: 0303-6898
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2012
    detail.hit.zdb_id: 186702-7
    detail.hit.zdb_id: 1466951-1
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  • 2
    In: Advanced Functional Materials, Wiley, Vol. 33, No. 22 ( 2023-05)
    Abstract: Many living tissues, such as muscle, become mechanically stronger with growth. Yet, synthetic hydrogels usually exhibit an opposite size‐mechanical property relation, that is, swelling‐weakening behavior. Herein, a series of swollen yet strengthened polyampholyte (PA) hydrogels are developed via a simple metal‐ion solution soaking strategy. In this strategy, a dynamic PA hydrogel (with ionic bonds) is dialyzed in ZrOCl 2 solutions (Step‐I) and deionized water (Step‐II) successively to obtain equilibrated hydrogels. Due to the specific Zr 4+ ions and PA network structure, Step‐I takes several months with sample size and mechanical performance increasing continuously, while Step‐II only needs several days. Through this strategy, the resultant hydrogel networks are reorganized and eventually constructed by ionic and metalligand bonds, enabling the swelling yet strengthening behavior. A systematic study confirms that dialysis time in Step‐I and corresponding ZrOCl 2 concentration can significantly affect the multiphase microstructures of the hydrogels, resulting in different mechanical enhancements. The optimized hydrogel possesses 39.2 MPa of Young's modulus and 3.7 MPa of tensile strength, which are 302 and 5.5 times these of the original PA gel, respectively. Despite distinct swelling, these hydrogels still mechanically surpass many existing high‐performance hydrogels. This study opens a novel pathway for fabricating swollen yet strengthened hydrogels.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
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  • 3
    Online Resource
    Online Resource
    Wiley ; 2013
    In:  Australian & New Zealand Journal of Statistics Vol. 55, No. 4 ( 2013-12), p. 421-434
    In: Australian & New Zealand Journal of Statistics, Wiley, Vol. 55, No. 4 ( 2013-12), p. 421-434
    Abstract: Exact simultaneous confidence bands (SCBs) for a polynomial regression model are available only in some special situations. In this paper, simultaneous confidence levels for both hyperbolic and constant width bands for a polynomial function over a given interval are expressed as multidimensional integrals. The dimension of these integrals is equal to the degree of the polynomial. Hence the values can be calculated quickly and accurately via numerical quadrature provided that the degree of the polynomial is small (e.g. 2 or 3). This allows the construction of exact SCBs for quadratic and cubic regression functions over any given interval and for any given design matrix. Quadratic and cubic regressions are frequently used to characterise dose response relationships in addition to many other applications. Comparison between the hyperbolic and constant width bands under both the average width and minimum volume confidence set criteria shows that the constant width band can be much less efficient than the hyperbolic band. For hyperbolic bands, comparison between the exact critical constant and conservative or approximate critical constants indicates that the exact critical constant can be substantially smaller than the conservative or approximate critical constants. Numerical examples from a dose response study are used to illustrate the methods.
    Type of Medium: Online Resource
    ISSN: 1369-1473 , 1467-842X
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2013
    detail.hit.zdb_id: 1468031-2
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