Malargüe seismic array: Design and deployment of the temporary array

2012 ◽  
Vol 127 (10) ◽  
Author(s):  
E. Ruigrok ◽  
D. Draganov ◽  
M. Gómez ◽  
J. Ruzzante ◽  
D. Torres ◽  
...  
Keyword(s):  
1971 ◽  
Author(s):  
R. R. Blandford ◽  
D. M. Clark
Keyword(s):  

Geophysics ◽  
2001 ◽  
Vol 66 (4) ◽  
pp. 1195-1207 ◽  
Author(s):  
Albin K. Kerekes

Deriving the response of an array is one thing, designing an array to match a desired response is quite another. The first is easy, the second is not. Given a selected pass and reject requirement in the spatial frequency domain, an array can be obtained that best matches such requirement within the limits of available hardware. Optimum spatial arrays for 2‐D and 3‐D/4‐D seismic surveys can be designed using the technique of spatial convolution. Such a technique relies upon uniform arrays of differing shapes and sizes as building blocks. These building blocks are convolved in space because their selected responses matching notch points against side lobes to achieve a desired end result in the spatial frequency domain. The final array design can be made optimum for a given set of requirements, such as signal preservation within the passband, attenuation within the reject band, and azimuthal distribution for 3‐D/4‐D seismic surveys. For any given design, solely the number and the spacing of the elements limit the optimization. A rule of thumb has been observed which shows that the required number of elements in a 2‐D array for 3‐D/4‐D seismic is equal to the square of the number of elements in a 1‐D equivalent array for 2‐D seismic. It is also observed that for a given number of elements, narrow azimuth designs can offer greater attenuation than wide azimuth designs.


1975 ◽  
Vol 65 (3) ◽  
pp. 787-788
Author(s):  
R. R. Blandford ◽  
D. M. Clark
Keyword(s):  

Author(s):  
Krishna Rudraraju Chaitanya ◽  
P. Mallikarjuna Rao ◽  
K. V. S. N. Raju ◽  
G. S. N. Raju

Author(s):  
Poovi Ganesan ◽  
N Damodharan

Background: A better understanding of the biopharmaceutical and physicochemical properties of drugs and the pharmaco-technical factors would be of great help for developing pharmaceutical products. But, it is extremely difficult to study the effect of each variable and interaction among them through the conventional approach Objective: To screen the most influential factors affecting the particle size (PS) of lipid nanoparticle (LNPs) (solid lipid nanoparticle (SLN) and nanostructured lipid carrier (NLC)) for poorly water-soluble BCS class-II drug like tamoxifen (TMX) to improve its oral bioavailability and to reduce its toxicity to tolerable limits using Taguchi (L12 (2 11)) orthogonal array design by applying computer optimization technique. Results: The size of all LNPs formulations prepared as per the experimental design varied between 172 nm and 3880 μm, polydispersity index between 0.033 and 1.00, encapsulation efficiency between 70.8% and 75.7%, and drug loading between 5.84% and 9.68%. The study showed spherical and non-spherical as well as aggregated and non-aggregated LNPs. Besides, it showed no interaction and amorphous form of the drug in LNPs formulation. The Blank NLCs exhibited no cytotoxicity on MCF-7 cells as compared to TMX solution, SLNs (F5) and NLCs (F12) suggests that the cause of cell death is primarily from the effect of TMX present in NLCs. Conclusions: The screening study clearly showed the importance of different individual factors significant effect for the LNPs formulation development and its overall performance in an in-vitro study with minimum experimentation thus saving considerable time, efforts, and resources for further in-depth study.


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