High efficiency photoresist-free lithography of UO3 patterns from amorphous films of uranyl complexes

1998 ◽  
Vol 13 (5) ◽  
pp. 1379-1389 ◽  
Author(s):  
M. Gao ◽  
Ross H. Hill

The solid state photochemistry of uranyl carboxylate complexes is presented with the purpose of developing methods for optical lithography of uranium oxide films. These complexes of the general formula, UO2(OOCR)2 (R = i-C3H7, C5H11, CH2C6H5, CH2OC2H5, C2H4OC2H5), were all photosensitive as thin amorphous films. The primary photochemical reaction for each of these complexes was the extrusion of a CO2 from the ligand and the production of radicals which initiated a chain reaction. The nature of this chain reaction was dependent upon the identity of the organic substituents, R. In some cases the chain reaction required a photochemical step while others were entirely thermal in nature. Of importance are the potentially high quantum yields which can be associated with thermal chain reactions. Some of the systems presented here exhibit quantum yields in excess of 1. This process was shown to be compatible with optical lithography by the patterning of the uranium oxide product on silicon surfaces.

1973 ◽  
Vol 51 (9) ◽  
pp. 1410-1415 ◽  
Author(s):  
Donna D. Carlson ◽  
Arthur R. Knight

The photolysis of C2H5SH liquid at 2537 Å has been shown to give H2 and C2H5SSC2H5 at equal rates with a quantum yield of 0.25. The photolysis of ethanethiol – methyl disulfide liquid mixtures leads, via a chain reaction involving propagation by attack of thiyl radicals on the disulfide S—S bond, to the formation with high quantum efficiency of CH3SH, C2H5SSC2H5 and, as an intermediate that is consumed after long exposures, CH3SSC2H5. The net result of the sequence of exchange processes is the essentially irreversible conversion of the methyl disulfide into methanethiol. The same overall reaction occurs thermally at room temperature, but the rate is appreciably less than that of the photochemical process. The quantum yields of formation of the unsymmetrical disulfides arising from the photochemically initiated exchange reaction in equimolar mixtures of CH3SSCH3 + n-C3H7SSC3H7 and C2H5SSC2H5 + n-C3H7SSC3H7 have been shown to be 6.9 and 4.4, compared to 355 for CH3-SSCH3 + C2H5SSC2H5 mixtures. In all three types of system examined in this investigation all thiyl radicals can be accounted for stoichiometrically on the basis of exchange and combination reactions alone, indicating negligible disproportionation of these species in condensed phase.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Tsuyoshi Fukushima ◽  
Yosuke Tanaka ◽  
Keito Adachi ◽  
Nanami Masuyama ◽  
Akiho Tsuchiya ◽  
...  

AbstractCell behavior is controlled by complex gene regulatory networks. Although studies have uncovered diverse roles of individual genes, it has been challenging to record or control sequential genetic events in living cells. In this study, we designed two cellular chain reaction systems that enable sequential sgRNA activation in mammalian cells using a nickase Cas9 tethering of a cytosine nucleotide deaminase (nCas9-CDA). In these systems, thymidine (T)-to-cytosine (C) substitutions in the scaffold region of the sgRNA or the TATA box-containing loxP sequence (TATAloxP) are corrected by the nCas9-CDA, leading to activation of the next sgRNA. These reactions can occur multiple times, resulting in cellular chain reactions. As a proof of concept, we established a chain reaction by repairing sgRNA scaffold mutations in 293 T cells. Importantly, the results obtained in yeast or in vitro did not match those obtained in mammalian cells, suggesting that in vivo chain reactions need to be optimized in appropriate cellular contexts. Our system may lay the foundation for building cellular chain reaction systems that have a broad utility in the future biomedical research.


2020 ◽  
Vol 38 (1) ◽  
pp. 39-44 ◽  
Author(s):  
Shalom Eliezer ◽  
Jose M. Martinez-Val

AbstractUsing a combination of laser–plasma interactions and magnetic confinement configurations, a conceptual fusion reactor is proposed in this paper. Our reactor consists of the following: (1) A background plasma of boron11 and hydrogen ions, plus electrons, is generated and kept for a certain time, with densities of the order of a mg/cm3 and temperatures of tens of eV. Both the radiation level and the plasma thermal pressure are thus very low. (2) A plasma channel is induced in a solid target by irradiation with a high power laser that creates a very intense shock wave. This mechanism conveys the acceleration of protons in the laser direction. The mechanisms must be tuned for the protons to reach a kinetic energy of 300–1200 keV where the pB11 fusion cross section is significantly large (note that this value is not a temperature). (3) Those ultra-fast protons enter the background plasma and collide with boron11 to produce three alphas. Fusion born alphas collide with protons of the plasma and accelerate them causing a chain reaction. (4) A combination of an induction current and a magnetic bottle keeps the chain reaction process going on, for a pulse long enough to get a high energy gain. (5) Materials for the background plasma and the laser target must be replaced for starting a new chain reaction cycle.


The homogeneous reaction between hydrogen and oxygen has been proved by the work of Hinshelwood, of Haber, and of Semenoff to be a chain reaction, which under certain conditions of temperature and pressure may pass over into an explosive combination. The reaction is subject to the kinetics characteristic of certain types of chain reactions, in that, for any particular temperature, there are upper and lower pressure limits for explosion, the former controlled by deactivation of the chains in the gas phase, and the latter by their termination at the surface. The conditions further point to a branching chain mechanism; below 300°C. there is no observable propagation of reaction chains. These facts seem to be well represented by the scheme of Bonhoeffer and Haber, which was put forward on the basis of a spectroscopic study of the dissociation of steam at high temperatures. H + H 2 + O 2 = HO + H 2 O + 102,000 cals. (1) HO + H 2 = H 2 O + H + 10,000 cals. (2) reaction (1) sometimes taking the alternative form H + H 2 + O 2 = OH + OH + H - 2000 cals. (1a) which accounts for the branching of the chains. Reaction (2) does not occur appreciably at temperatures below 300°C., but the OH radicles yield hydrogen peroxide which may be detected.


2021 ◽  
Author(s):  
Tsuyoshi Fukushima ◽  
Yosuke Tanaka ◽  
Keito Adachi ◽  
Nanami Masuyama ◽  
Shuhei Asada ◽  
...  

Abstract Cellular behavior is governed by the complex gene regulatory networks. Although studies have revealed diverse roles of individual genes, it has been a challenge to record or control the sequential genetic events in living cells. In this study, we designed two cellular chain reaction systems that enable sequential sgRNA expression in mammalian cells using a nickase Cas9 tethering of a cytosine nucleotide deaminase (nCas9-CDA). In these systems, the thymidine (T)-to-cytosine (C) substitutions in the scaffold region of sgRNA or TATA box containing loxP sequence (TATAloxP) are corrected by the nCas9-CDA, which leads to expression of next sgRNA. These reactions can proceed several times, thus generating cellular chain reactions. As a proof of the concept, we established a chain reaction through the repair of sgRNA scaffold mutations in 293T cells. Importantly, the results obtained in yeast or in vitro were not consistent with those in mammalian cells, suggesting that the in vivo chain reactions need to be optimized in appropriate cellular contexts. Our system may lay the foundation for building cellular chain reaction systems that have a broad utility in the future biomedical research.


1963 ◽  
Vol 10 (02) ◽  
pp. 400-405 ◽  
Author(s):  
B. A Amundson ◽  
L. O Pilgeram

SummaryEnovid (5 mg norethynodrel and 0.075 mg ethynylestradiol-3-methyl ether) therapy in young normal human subjects causes an increase in plasma fibrinogen of 32.4% (P >C 0.001). Consideration of this effect together with other effects of Enovid on the activity of specific blood coagulatory factors suggests that the steroids are exerting their effect at a specific site of the blood coagulation and/or fibrinolytic system. The broad spectrum of changes which are induced by the steroids may be attributed to a combination of a chain reaction and feed-back control.


2021 ◽  
Vol 11 (2) ◽  
pp. 77-93
Author(s):  
Khalid O. Alfarouk ◽  
Sari T. S. AlHoufie ◽  
Samrein B. M. Ahmed ◽  
Mona Shabana ◽  
Ahmed Ahmed ◽  
...  

COVID-19, occurring due to SARS-COV-2 infection, is the most recent pandemic disease that has led to three million deaths at the time of writing. A great deal of effort has been directed towards altering the virus trajectory and/or managing the interactions of the virus with its subsequent targets in the human body; these interactions can lead to a chain reaction-like state manifested by a cytokine storm and progress to multiple organ failure. During cytokine storms the ratio of pro-inflammatory to anti-inflammatory mediators is generally increased, which contributes to the instigation of hyper-inflammation and confers advantages to the virus. Because cytokine expression patterns fluctuate from one person to another and even within the same person from one time to another, we suggest a road map of COVID-19 management using an individual approach instead of focusing on the blockbuster process (one treatment for most people, if not all). Here, we highlight the biology of the virus, study the interaction between the virus and humans, and present potential pharmacological and non-pharmacological modulators that might contribute to the global war against SARS-COV-2. We suggest an algorithmic roadmap to manage COVID-19.


1980 ◽  
Vol 20 (18) ◽  
pp. 1197-1204 ◽  
Author(s):  
H. T. Chen ◽  
P. A. Chartier ◽  
S. Setthachayanon

Author(s):  
Shanzhong Duan ◽  
Kurt S. Anderson

Abstract The paper presents a new hybrid parallelizable low order algorithm for modeling the dynamic behavior of multi-rigid-body chain systems. The method is based on cutting certain system interbody joints so that largely independent multibody subchain systems are formed. These subchains interact with one another through associated unknown constraint forces f¯c at the cut joints. The increased parallelism is obtainable through cutting the joints and the explicit determination of associated constraint loads combined with a sequential O(n) procedure. In other words, sequential O(n) procedures are performed to form and solve equations of motion within subchains and parallel strategies are used to form and solve constraint equations between subchains in parallel. The algorithm can easily accommodate the available number of processors while maintaining high efficiency. An O[(n+m)Np+m(1+γ)Np+mγlog2Np](0<γ<1) performance will be achieved with Np processors for a chain system with n degrees of freedom and m constraints due to cutting of interbody joints.


Sign in / Sign up

Export Citation Format

Share Document