Impedance and Photosensitivity Spectra of Nanocomposite Structures Based on Layered Semiconductor InSe and Ionic Salt RbNO3

2018 ◽  
Vol 215 (24) ◽  
pp. 1800460
Author(s):  
Anatoliy P. Bakhtinov ◽  
Volodymyr M. Vodopyanov ◽  
Volodymyr I. Ivanov ◽  
Ivan G. Tkachuk ◽  
Viktor V. Netyaga ◽  
...  
2015 ◽  
Vol 273 ◽  
pp. 59-65 ◽  
Author(s):  
A.P. Bakhtinov ◽  
V.M. Vodopyanov ◽  
Z.R. Kudrynskyi ◽  
Z.D. Kovalyuk ◽  
V.V. Netyaga ◽  
...  

Agronomy ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 435
Author(s):  
Agnieszka Ludwiczak ◽  
Monika Osiak ◽  
Stefany Cárdenas-Pérez ◽  
Sandra Lubińska-Mielińska ◽  
Agnieszka Piernik

Salinization is a key soil degradation process. An estimated 20% of total cultivated lands and 33% of irrigated agricultural lands worldwide are affected by high salinity. Much research has investigated the influence of salt (mainly NaCl) on plants, but very little is known about how this is related to natural salinity and osmotic stress. Therefore, our study was conducted to determine the osmotic and ionic salt stress responses of selected C3 and C4 cultivated plants. We focused on the early growth stages as those critical for plant development. We applied natural brine to simulate natural salinity and to compare its effect to NaCl solution. We assessed traits related to germination ability, seedlings and plantlet morphology, growth indexes, and biomass and water accumulation. Our results demonstrate that the effects of salinity on growth are strongest among plantlets. Salinity most affected water absorption in C3 plants (28% of total traits variation), but plant length in C4 plants (17–27%). Compensatory effect of ions from brine were suggested by the higher model plants’ growth success of ca 5–7% under brine compared to the NaCl condition. However, trait differences indicated that osmotic stress was the main stress factor affecting the studied plants.


2015 ◽  
Vol 39 ◽  
pp. 25-33
Author(s):  
Ahmet GÜLTEK ◽  
Davut AKSÜT ◽  
Turgay SEÇKİN ◽  
Emre BİRHANLI ◽  
Mert Olgun KARATAŞ ◽  
...  

2014 ◽  
Vol 9 (12) ◽  
pp. 1024-1030 ◽  
Author(s):  
Xidong Duan ◽  
Chen Wang ◽  
Jonathan C. Shaw ◽  
Rui Cheng ◽  
Yu Chen ◽  
...  

1996 ◽  
Vol 53 (22) ◽  
pp. 14806-14817 ◽  
Author(s):  
H. C. Hsueh ◽  
M. C. Warren ◽  
H. Vass ◽  
G. J. Ackland ◽  
S. J. Clark ◽  
...  

2004 ◽  
Vol 9 (1-3) ◽  
pp. 177-196 ◽  
Author(s):  
Rohitkumar H. Vora ◽  
P. Santhana Gopala Krishnan ◽  
S. Veeramani
Keyword(s):  

2012 ◽  
Vol 1421 ◽  
Author(s):  
Russell J. Bailey ◽  
Remco Geurts ◽  
Debbie J. Stokes ◽  
Frank de Jong ◽  
Asa H. Barber

ABSTRACTThe mechanical behavior of nanocomposites is critically dependent on their structural composition. In this paper we use Focused Ion Beam (FIB) microscopy to prepare surfaces from a layered polymer nanocomposite for investigation using phase contrast atomic force microscopy (AFM). Phase contrast AFM provides mechanical information on the surface examined and, by combining with the sequential cross-sectioning of FIB, can extend the phase contract AFM into three dimensions.


1998 ◽  
Vol 76 (12) ◽  
pp. 1844-1852
Author(s):  
Fernande D Rochon ◽  
Robert Melanson ◽  
Margaret M Kayser

At lower temperatures stabilized ylides react with unsymmetrically substituted phthalic anhydrides to give two acyclic adducts. When the reactions are allowed to proceed at higher temperature enol lactones are formed. Identification of the acyclic intermediates was necessary to understand the mechanism of these Wittig reactions. The transient species trapped in the reaction with trimethyloxonium tetrafluoroborate were unambiguously identified by crystallographic methods. The crystal structures of the tetrafluoroborate salt of methyl(triphenylphosphoranyl idene)- acetate (8), methyl(3-methoxy,2-methoxycarbonylbenzoyl)triphenylphosphoranylideneacetate (6β), and methyl(2-methoxycarbonyl,6-nitrobenzoyl)triphenylphosphoranylideneacetate (7α) were studied by X-ray diffraction. The ionic salt (8) is monoclinic, P21c,a= 12.640(5), b = 13.945(9), c = 14.825(6) Å, β = 125.32(3)°, Z = 4, and R = 0.065 (F >5.4 σ(F)). Crystal 6 β is monoclinic, P21c,a = 16.391(16), b = 9.029(6), c = 19.835(19) Å, β = 116.60(6)°, Z = 4, and R = 0.070 (F > 4.6 σ(F)), while crystal 7α is also monoclinic, P21c,a = 9.513(5), b = 9.361(3), c = 30.908(13) Å, β = 98.42(3)°, Z = 4, and R = 0.057 (F >5 σ(F)). In the BF 4- salt (12), the four P-C distances are equal (1.791(5)-1.801(7) Å) with identical tetrahedral angles. For the two triphenylphosphoranylideneacetate compounds, the fourth P-C(1) bond is shorter (1.762(6)-1.734(5) Å) than the three P-C(Ph) bonds (avg. 1.809(5) Å). The angles C(1)-P-C(Ph) are also larger (avg. 112.9(2)° for 6β and 111.9(2)° for 7α) than the C(Ph)-P-C(Ph) angles (avg. 105.8(2)° for 6 β and 106.9(2)° for 7α). These values suggest a multiple nature for the P-C(1) bond. In the nitro derivative, the nitro and the ester groups are disordered equally in positions 2 and 6. Key words: Wittig reactions, cyclic anhydrides, stabilized ylide, phosphoranylidenes, crystal structures.


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