EFFECT OF THE CALCINATION TEMPERATURE ON THE DIELECTRIC PROPERTIES OF 0.94NA0.5BI0.5TIO3–0.06BATIO3 CERAMICS

2020 ◽  
Vol 27 (10) ◽  
pp. 1950222
Author(s):  
RUIFANG WU ◽  
RUIJIE DUAN ◽  
LINLIN LIANG ◽  
GANG BIAN ◽  
JING WANG

With the miniaturization of electronic products, the portability and the critical need of clean energy for environment have led to the development of lead-free electroceramics. In this work, lead-free dielectric ceramics of 0.94Na[Formula: see text]Bi[Formula: see text]TiO3–0.06BaTiO3 (NBT–0.06BT) are synthesized by wet solid-phase method. The effects of calcination temperature on phase structure, morphology, densification behavior and dielectric properties are investigated. The XRD results indicate that all samples demonstrate typical diffraction peaks of perovskite structure. The SEM and dielectric analytical results show that high-performance dielectric property of NBT–0.06BT ceramic with dense microstructure and appropriate grain size can be achieved when the calcination temperature is appropriate.

1986 ◽  
Vol 32 (5) ◽  
pp. 890-893 ◽  
Author(s):  
P T Pollak ◽  
S G Carruthers ◽  
D J Freeman

Abstract We describe a rapid, simplified isocratic "high-performance" liquid-chromatographic method for simultaneous measurement of the antiarrhythmic drug amiodarone and its major metabolite, desethylamiodarone, in small volumes of sera (100 microL). Compared with liquid-liquid extraction, the solid-phase method of extraction saves time and glassware and improves reproducibility for small sample volumes. Amiodarone and desethylamiodarone could be measured at concentrations as low as 250 micrograms/L. Standard curves for the drug and metabolite are linear over the range of concentrations found in our patients. Within-run CVs (n = 6) ranged from 2.7% to 4.5% for amiodarone and from 4.0% to 5.7% for desethylamiodarone over the range of 250 to 4000 micrograms/L. Between-run CVs (n = 12) were 8.3% and 5.7% for amiodarone and desethylamiodarone, respectively. Commonly used cardiovascular medications do not interfere with the assay.


RSC Advances ◽  
2016 ◽  
Vol 6 (70) ◽  
pp. 65644-65653 ◽  
Author(s):  
Xiaohong Wang ◽  
Fangsheng Wu ◽  
Yawei Duan ◽  
Yingying Wang ◽  
Chen Hao ◽  
...  

CuO nanostructures were successfully synthesized using NaOH and Cu(NO3)2 as starting materials by an aminated lignin (AL)-assisted solid-phase method.


2017 ◽  
Vol 5 (21) ◽  
pp. 10261-10268 ◽  
Author(s):  
Pingyuan Feng ◽  
Wei Wang ◽  
Kangli Wang ◽  
Shijie Cheng ◽  
Kai Jiang

Na3V2(PO4)3/C, as a high-performance cathode material for sodium ion batteries, was synthesized via a facile agarose-assisted solid-phase method.


Author(s):  
V.A. Artyukh ◽  
◽  
V.N. Borsch ◽  
V.S. Yusupov ◽  
S.Ya. Zhuk ◽  
...  

1988 ◽  
Vol 53 (11) ◽  
pp. 2914-2919 ◽  
Author(s):  
Pierrette Maes ◽  
Annie Ricouart ◽  
Emmanuel Escher ◽  
André Tartar ◽  
Christian Sergheraert

Analogs of angiotensin II in which phenylalanine in position 8 was replaced with cymantrenylalanine or with its triphenylphosphine photosubstitution product were synthesized by the solid-phase method. On rabbit aorta strips, these peptides were found to be pure antagonists of angiotensin II. Their relative affinities are higher than most other analogs substituted in position 8 with bulky amino-acids.


1991 ◽  
Vol 56 (2) ◽  
pp. 491-498 ◽  
Author(s):  
Bernard Lammek ◽  
Izabela Derdowska ◽  
Tomasz M. Wierzba ◽  
Witold Juzwa

In an attempt to determine some of the structural features in position 1 that account for V1 antagonism, four new analogues of arginine-vasopressin were synthesized and the effect of the modifications on the vasoconstrictor activity was checked using isolated mesenteric arterial vessels of rats. The protected precursors required for these analogues were synthesized by a solid phase method of peptide synthesis. One of the reported analogues, namely [1-(4-mercapto-4-tetrahydrothiopyraneacetic acid)., 2-O-methyltyrosine, 8-arginine]vasopressin appears to be a potent competitive antagonist of the vasoconstrictor effect by AVP.


1981 ◽  
Vol 362 (2) ◽  
pp. 833-840 ◽  
Author(s):  
Eric ATHERTON ◽  
Willy HÜBSCHER ◽  
Robert C. SHEPPARD ◽  
Vivienne WOOLLEY

2001 ◽  
Vol 10 (2) ◽  
pp. 89-92 ◽  
Author(s):  
T. Abiko ◽  
R. Ogawa

Two {Met(0)6}deacetyl-thymosin β4analogs containing Phe(4F) or Tyr(Me) at position 12 were synthesized by the manual solid-phase method, and their anti-inflammatory effect on carrageenin-induced edema in the mouse paw was studied. Fluorination of the para-position of Phe12resulted in a marked antiinflammatory effect on carrageenin-induced edema in the mouse paw compared with that of our synthetic {Met(0)6}deacetyl-thymosin β4, but the other analog, {Met(0)6, Tyr(Me)12}deacetyl-thymosin β4, showed a marked reduction of the anti-inflammatory effect.


1994 ◽  
Vol 59 (2) ◽  
pp. 461-466 ◽  
Author(s):  
Vladimir A. Basiuk ◽  
Taras Yu. Gromovoy

The "gas solid-phase" method is used for the preparation of both symmetric and asymmetric 2,5-dioxopiperazines via cyclization of vaporous linear dipeptides in the presence of silica.


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