User:Mary Mendoza/Notebook/CHEM 581: Experimental Chemistry I/2014/10/31: Difference between revisions
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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span> | |style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span> | ||
|style="background-color: #F2F2F2" align="center"| | |style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]] }}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}} | ||
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== | ==Continuation of Bead Synthesis Trials== | ||
* | * The burette set-up utilized by Eleni, Melvin, and Becca's group will be used; details of their assembly can be found on Kalivas' entry for [[User:Eleni N. Kalivas/Notebook/CHEM-571/2014/10/29|10/29/2014]]. | ||
* The assembly was prepared as shown in the picture. | |||
[[Image:IMG 3226.JPG|thumb|center|600x600px]] | |||
==Description== | |||
# A column was set up with glutaraldehyde and hexane. Air is being bubbled through the column to mix the two liquids. | |||
# PVA-Clay will be dropped down the column | |||
<u>Hexane Trial</u> | |||
* The PVA-Clay formed beads within the hexane and floated down the column. They did not cross-link fast enough if at all and they dissolved into the glutaraldehyde. | |||
<u>Organic-Glutaraldehyde Solution</u> | |||
* We attempted to add acetone to glutaraldehyde and then add hexane to get rid of the solvent layers. The solution was not hydrophobic enough to form beads however. When only a slight layer of hexane and stirring were applied, it yielded no good results. | |||
# We have decided to abandon the beads and begin synthesis of ribbons | |||
## We filled a column with acetone and 1.5mL of Glutaraldehyde | |||
## we then dropped in the PVA-Clay | |||
==Trial of Several Organic Solvents== | |||
* ''I observed that as soon as the organic phase, formed bead comes into contact with the aqueous phase of the glutaraldehyde, the bead disperses into the aqueous solution. I decided to conduct my own trials and have my group members continue the burette-ribbon experiments.'' | |||
* ''I concluded that the dilemma in the formation of beads is the immiscibility of the organic phase which forms the beads and the aqueous phase that cross-links the beads.'' | |||
* ''Therefore, I thought, I can resolve this issue by choosing several organic solvents slightly miscible with water but hydrophobic enough to form the beads.'' | |||
* ''In an attempt to keep the reaction mixture homogenized, motion is required. Thus, the reaction should be kept stirring on a stir plate. Also, stirring prevents the formed beads from clumping together." | |||
* I used the solvent miscibility table provided by Dr. Hartings taken from chemical company, phenomenex, as shown in the picture. | |||
[[Image:Solvent miscibility chart.jpg|thumb|center|494x599px]] | |||
<u>Acetonitrile Trial</u> | |||
* A drop of the PVA-clay was added into 3 mL of acetonitrile contained in a 12x100 mm, 8 mL disposable test tube. | |||
* The PVA-clay did not form beads. | |||
* Acetonitrile was tested without the use of the solvent miscibility chart. Upon checking the chart, the solubility in water of acetonitrile (%w/w) is 100. | |||
<u>DMSO and Ethyl Acetate</u> | |||
* Hence, I selected the top 5 least immiscible organic solvent according to their solubility in water (%w/w) as shown in the picture. | |||
* I first tested dimethyl sulfoxide (DMSO) and ethyl acetate. For DMSO, a quick formation of bead was observed but readily dispersed as it settled on the bottom of the tube. On the other hand, as the drop of PVA-clay-HCl passed through the ethyl acetate, the bead retained its shape for at least 5 to 7 seconds and gradually dispersed. | |||
* Without testing the remaining organic solvents, I chose ethyl acetate as my organic solvent. It had the suitable features such that it enables the bead formation and its slight immiscibility with water. | |||
* Next, it was time to test ethyl acetate with glutaraldehyde. The following amounts for the ethyl acetate trial were not exactly measured but made by approximation. I took a 50 mL beaker with a magnetic stir bar. I approximately added 15-20 mL of ethyl acetate. In a drop wise manner, I added my PVA-clay-HCl solution using a pasteur pipette. I added at least 500 uL of glutaraldehyde. | |||
* With this experimental set-up, I was able to form beads but had to resolve the ratio of materials I used since everything was performed by approximation. | |||
[[Image:Solvents.png|center]] | |||
Latest revision as of 00:29, 27 September 2017
Project name | Main project page Previous entry Next entry |
Continuation of Bead Synthesis Trials
Description
Hexane Trial
Organic-Glutaraldehyde Solution
Trial of Several Organic Solvents
Acetonitrile Trial
DMSO and Ethyl Acetate
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