Garment Pleats Modeling and Force Analysis Based on Different Yarn Directions

Blood fever and Chikungunya cases in Indonesia are increasing annually. For preventing the mosquios, people use mosquito coil which is contain dangerous chemical compound. This research has successly created a natural mosquito coil with gemor bark and hazelnut fruit shell as the main material. Gemor bark is positive containing alcaloid,tanin, phenolk, flvonoid, triterpnoid and glycocydic compounds which are natural bioinsecticide. As formulation the comparison of gemor bark and hazelnut shell as follow :100% : 0 % ; 80 % : 20 % ; 65 % : 35 % ; 50 % : 50 % ; 35 % : 65% and 20 % : 80% were used. Base one random variance analysis, the best formula was the using of gemor bark in 50%, 35% and 20% of concentration. The mosquitos killing force analysis was using the LT50 for 6 days with 5 diferent concentrations. The result showed that 50 % of gemor bark was significantly influenced in the killing force. From the economic view, the producion of this coil was cheaper then the same product in the maket. Base on all the result, the research product is applicable in mass producion and safe for human health and the environment.Keywords: gemor bark , hazelnut fruit shell , mosquito coil, natural , ecofriendly

Download Full-text

THE FORCE ANALYSIS OF THE CATERPILLAR EXCAVATOR STICK ARRANGEMENT MECHANISM WITH THREE DEGREES OF FREEDOM

MINING INFORMATIONAL AND ANALYTICAL BULLETIN ◽

10.25018/0236-1493-2018-1-0-133-142 ◽

2018 ◽

Vol 1 ◽

pp. 133-142 ◽

Cited By ~ 5

Author(s):

A.M. Busygin ◽

Keyword(s):

Degrees Of Freedom ◽

Force Analysis ◽

Three Degrees Of Freedom

Download Full-text

Intramolecular Proton Transfer in the Isomerization of Hydroxyacetone: A Detailed Characterization Based on Reaction Force Analysis and the Bond Fragility Spectrum

10.26434/chemrxiv.12049062 ◽

2020 ◽

Author(s):

Wallace Derricotte ◽

Huiet Joseph

Keyword(s):

Chemical Potential ◽

Reaction Force ◽

Intramolecular Proton Transfer ◽

Intermediate Energy ◽

Force Analysis ◽

Activation Energy Barrier ◽

Detailed Characterization ◽

Proton Transfers ◽

Reaction Force Constant

The mechanism of isomerization of hydroxyacetone to 2-hydroxypropanal is studied within the framework of reaction force analysis at the M06-2X/6-311++G(d,p) level of theory. Three unique pathways are considered: (i) a step-wise mechanism that proceeds through formation of the Z-isomer of their shared enediol intermediate, (ii) a step-wise mechanism that forms the E-isomer of the enediol, and (iii) a concerted pathway that bypasses the enediol intermediate. Energy calculations show that the concerted pathway has the lowest activation energy barrier at 45.7 kcal mol<sup>-1</sup>. The reaction force, chemical potential, and reaction electronic flux are calculated for each reaction to characterize electronic changes throughout the mechanism. The reaction force constant is calculated in order to investigate the synchronous/asynchronous nature of the concerted intramolecular proton transfers involved. Additional characterization of synchronicity is provided by calculating the bond fragility spectrum for each mechanism.

Download Full-text