Three-Dimensional Stretchable Microelectronics by Projection Microstereolithography (PμSL)

2021 ◽  
Vol 13 (7) ◽  
pp. 8901-8908
Author(s):  
Yuejiao Wang ◽  
Xiang Li ◽  
Sufeng Fan ◽  
Xiaobin Feng ◽  
Ke Cao ◽  
...  
Keyword(s):  
Three Dimensional ◽  
Projection Microstereolithography

Fabrication of chiral channel in three-dimensional photonic crystal using projection microstereolithography

Optik ◽  
2019 ◽  
Vol 185 ◽  
pp. 1045-1050
Author(s):  
En-Tao Liang ◽  
Wei-Xing Zhang ◽  
Yi-Gui Chen ◽  
Han Shen ◽  
Fu-Li Zhao ◽  
...  
Keyword(s):  
Photonic Crystal ◽  
Three Dimensional ◽  
Dimensional Photonic Crystal ◽  
Projection Microstereolithography

Three-dimensional grayscale for improving surface quality in projection microstereolithography

2012 ◽  
Vol 13 (2) ◽  
pp. 291-298 ◽  
Author(s):  
In-Baek Park ◽  
Young-Myoung Ha ◽  
Min-Sub Kim ◽  
Ho-Chan Kim ◽  
Seok-Hee Lee
Keyword(s):  
Surface Quality ◽  
Three Dimensional ◽  
Projection Microstereolithography

Material Property Manipulation of Photopolymer Vibration Energy Harvesters

2012 ◽  
Author(s):  
Evan Baker ◽  
Timothy Reissman ◽  
Fan Zhou ◽  
Cheng Sun
Keyword(s):  
Flexural Rigidity ◽  
Three Dimensional ◽  
Effective Elastic Modulus ◽  
Electrical Energy ◽  
Vibration Energy ◽  
Energy Harvesters ◽  
Post Process ◽  
Naturally Occurring ◽  
Output Increase ◽  
Projection Microstereolithography

The inefficiency in converting naturally occurring vibration frequencies (sub-100 Hz) to electrical energy continues to be a major obstacle for miniaturized vibration energy harvesters. In a recent work, we addressed this issue by introducing photopolymer-based designs, using projection microstereolithography which exhibited 61 Hz resonant frequencies due to low elastic moduli and low flexural rigidity using a three-dimensional, helical coil design. In this paper, we extend upon those findings to report on a post-process technique which uses ultraviolet exposure time to manipulate the material properties of photopolymer-based vibration energy harvesters. The results show with 1–3 minutes of post-exposure, an effective elastic modulus variation from 399–904 MPa and a parasitic damping change from 0.0595–0.0986 kgs−1. Likewise, resonant frequency shifts of 53.5–805 Hz and power output increase from 56.5 to 120.4 μW (when excited at a constant acceleration of 6.06±0.06 ms−2) are achieved, without geometry changes and using the same photopolymer material.

The orbit of Pluto over a long interval of time

1966 ◽  
Vol 25 ◽  
pp. 227-229 ◽  
Author(s):  
D. Brouwer
Keyword(s):  
Periodic Orbit ◽  
Numerical Integration ◽  
Restricted Problem ◽  
Three Dimensional ◽  
The Third ◽  
Circular Restricted Problem ◽  
Resonance Relation

The paper presents a summary of the results obtained by C. J. Cohen and E. C. Hubbard, who established by numerical integration that a resonance relation exists between the orbits of Neptune and Pluto. The problem may be explored further by approximating the motion of Pluto by that of a particle with negligible mass in the three-dimensional (circular) restricted problem. The mass of Pluto and the eccentricity of Neptune's orbit are ignored in this approximation. Significant features of the problem appear to be the presence of two critical arguments and the possibility that the orbit may be related to a periodic orbit of the third kind.

Conformation of Ribosomes from Escherichia Coli

1974 ◽  
Vol 32 ◽  
pp. 210-211
Author(s):  
M. Boublik ◽  
W. Hellmann ◽  
F. Jenkins
Keyword(s):  
Binding Sites ◽  
Ribosomal Proteins ◽  
Fluorescent Dyes ◽  
Protein Biosynthesis ◽  
Three Dimensional ◽  
Spatial Arrangement ◽  
Dimensional Structure ◽  
Complete Understanding ◽  
And Function

The present knowledge of the three-dimensional structure of ribosomes is far too limited to enable a complete understanding of the various roles which ribosomes play in protein biosynthesis. The spatial arrangement of proteins and ribonuclec acids in ribosomes can be analysed in many ways. Determination of binding sites for individual proteins on ribonuclec acid and locations of the mutual positions of proteins on the ribosome using labeling with fluorescent dyes, cross-linking reagents, neutron-diffraction or antibodies against ribosomal proteins seem to be most successful approaches. Structure and function of ribosomes can be correlated be depleting the complete ribosomes of some proteins to the functionally inactive core and by subsequent partial reconstitution in order to regain active ribosomal particles.

Ultrastructural Investigations of the Contractile Filaments of Amoebae

1974 ◽  
Vol 32 ◽  
pp. 188-189
Author(s):  
P.L. Moore
Keyword(s):  
Cytoplasmic Streaming ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Amoeboid Movement ◽  
Different Types ◽  
Chemical Conditions ◽  
Complete Interpretation

Previous freeze fracture results on the intact giant, amoeba Chaos carolinensis indicated the presence of a fibrillar arrangement of filaments within the cytoplasm. A complete interpretation of the three dimensional ultrastructure of these structures, and their possible role in amoeboid movement was not possible, since comparable results could not be obtained with conventional fixation of intact amoebae. Progress in interpreting the freeze fracture images of amoebae required a more thorough understanding of the different types of filaments present in amoebae, and of the ways in which they could be organized while remaining functional.The recent development of a calcium sensitive, demembranated, amoeboid model of Chaos carolinensis has made it possible to achieve a better understanding of such functional arrangements of amoeboid filaments. In these models the motility of demembranated cytoplasm can be controlled in vitro, and the chemical conditions necessary for contractility, and cytoplasmic streaming can be investigated. It is clear from these studies that “fibrils” exist in amoeboid models, and that they are capable of contracting along their length under conditions similar to those which cause contraction in vertebrate muscles.

Structural organization of escherichia coli ribosomes as determined by immuno electron microscopy

1978 ◽  
Vol 36 (2) ◽  
pp. 166-167 ◽  
Author(s):  
G. Stöffler ◽  
R.W. Bald ◽  
J. Dieckhoff ◽  
H. Eckhard ◽  
R. Lührmann ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Escherichia Coli ◽  
Ribosomal Proteins ◽  
Structural Organization ◽  
Three Dimensional ◽  
Ribosomal Subunit ◽  
Spatial Arrangement ◽  
Small Subunit ◽  
Antibody Binding ◽  
Immuno Electron Microscopy

A central step towards an understanding of the structure and function of the Escherichia coli ribosome, a large multicomponent assembly, is the elucidation of the spatial arrangement of its 54 proteins and its three rRNA molecules. The structural organization of ribosomal components has been investigated by a number of experimental approaches. Specific antibodies directed against each of the 54 ribosomal proteins of Escherichia coli have been performed to examine antibody-subunit complexes by electron microscopy. The position of the bound antibody, specific for a particular protein, can be determined; it indicates the location of the corresponding protein on the ribosomal surface.The three-dimensional distribution of each of the 21 small subunit proteins on the ribosomal surface has been determined by immuno electron microscopy: the 21 proteins have been found exposed with altogether 43 antibody binding sites. Each one of 12 proteins showed antibody binding at remote positions on the subunit surface, indicating highly extended conformations of the proteins concerned within the 30S ribosomal subunit; the remaining proteins are, however, not necessarily globular in shape (Fig. 1).

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