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Shin, Dong Won,Lee, So Young,Lee, Chang Hyun,Lee, Kwan-Soo,Park, Chi Hoon,McGrath, James E.,Zhang, Mingqiang,Moore, Robert B.,Lingwood, Mark D.,Madsen, Louis A.,Kim, Young Taek,Hwang, Inchul,Lee, Youn American Chemical Society 2013 Macromolecules Vol.46 No.19
<P>Ordered morphologies in disulfonated poly(arylene sulfide sulfone nitrile) (SPSN) copolymers were generated via thermal annealing followed by multiblock copolymer synthesis. While SPSN random copolymers (R-SPSN) showed featureless morphologies, the SPSN multiblock copolymers (B-SPSN) exhibited cocontinuous lamellar morphologies with a center-to-center interdomain size of up to 40 nm. In spite of the well-ordered, interconnected hydrophilic domains, the water self-diffusion coefficient (e.g., <I>D</I> = (0.7–2.0) × 10<SUP>–10</SUP> m<SUP>2</SUP> s<SUP>–1</SUP>) and proton conductivity (e.g., σ = 0.16–0.20 S cm<SUP>–1</SUP> in deionized water at 30 °C) through B-SPSN were lower than those of the corresponding R-SPSN (e.g., <I>D</I> = (3.5–3.9) × 10<SUP>–10</SUP> m<SUP>2</SUP> s<SUP>–1</SUP> and σ = 0.21 S cm<SUP>–1</SUP>) due to the relatively lower water uptake of the B-SPSN after thermal annealing. The reduced water uptake of B-SPSN was beneficial to reduction of peroxide degradation rate. Thermal annealing produced significant gains in morphological ordering and finer control over desired membrane properties for proton conduction applications.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/mamobx/2013/mamobx.2013.46.issue-19/ma400889t/production/images/medium/ma-2013-00889t_0010.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/ma400889t'>ACS Electronic Supporting Info</A></P>
Structure-property relationships for a series of amorphous partially aliphatic polyimides
Eichstadt, Amy E.,Ward, Thomas C.,Bagwell, Melanie D.,Farr, Isaac V.,Dunson, Debra L.,McGrath, James E. Wiley Subscription Services, Inc., A Wiley Company 2002 Journal of polymer science. Part B, Polymer physic Vol.40 No.14
<P>High molecular weight, soluble, amorphous, partially aliphatic polyimides were successfully synthesized using an ester acid high-temperature solution imidization route, which allows one to control desired glass-transition (T<SUB>g</SUB>) and processing temperatures. This method involves the prereaction of aromatic dianhydrides with ethanol and a tertiary amine catalyst to form ester acids, followed by the addition of diamines. Subsequent thermal reaction forms fully cyclized polyimides. This reaction pathway eliminates the need for anhydrous solvents and overcomes the problem of salt formation commonly observed for nucleophilic, more-basic aliphatic amines when utilizing the traditional polyamic acid synthesis route. The molar ratio of aromatic-to-aliphatic diamines was varied to generate a series of copolyimides with the chosen dianhydride and tailor the physical properties for specific adhesive applications. This series of copolyimides was characterized by their molecular weight, T<SUB>g</SUB>, thermal stability, coefficient of thermal expansion, refractive index, and dielectric constant. Structure-property relationships were established. The γ and β sub-T<SUB>g</SUB> viscoelastic properties were researched to understand their molecular origins. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 1503–1512, 2002</P>
Alyna Turner,John J. McGrath,Olivia M. Dean,Seetal Dodd,Andrea Baker,Susan M. Cotton,James G. Scott,Bianca E. Kavanagh,Melanie M. Ashton,Adam J. Walker,Ellie Brown,MIchael Berk 대한정신약물학회 2019 CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE Vol.17 No.2
Objective: Garcinia mangostana Linn., commonly known as mangosteen, is a tropical fruit with a thick pericarp rind containing bioactive compounds that may be beneficial as an adjunctive treatment for schizophrenia. The biological underpinnings of schizophrenia are believed to involve altered neurotransmission, inflammation, redox systems, mitochondrial dysfunction, and neurogenesis. Mangosteen pericarp contains xanthones which may target these biological pathways and improve symptoms; this is supported by preclinical evidence. Here we outline the protocol for a double- blind randomized placebo-controlled trial evaluating the efficacy of adjunctive mangosteen pericarp (1,000 mg/day), compared to placebo, in the treatment of schizophrenia. Methods: We aim to recruit 150 participants across two sites (Geelong and Brisbane). Participants diagnosed with schizophrenia or schizoaffective disorder will be randomized to receive 24 weeks of either adjunctive 1,000 mg/day of mangosteen pericarp or matched placebo, in addition to their usual treatment. The primary outcome measure is mean change in the Positive and Negative Symptom Scale (total score) over the 24 weeks. Secondary outcomes include positive and negative symptoms, general psychopathology, clinical global severity and improvement, depressive symptoms, life satisfaction, functioning, participants reported overall improvement, substance use, cognition, safety and biological data. A 4-week post treatment interview at week 28 will explore post-discontinuations effects. Results: Ethical and governance approvals were gained and the trial commenced. Conclusion: A positive finding in this study has the potential to provide a new adjunctive treatment option for people with schizophrenia and schizoaffective disorder. It may also lead to a greater understanding of the pathophysiology of the disorder.