Category: NRG

PDMS, diffusion and pressurization update

I’m having trouble getting the PDMS to cure on the NC. When I first started these experiments in August, the PDMS seemed to cure on the NC without a problem. Now, when I remove the PDMS + NC from the

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Original Contact Angle Study

This is the original contact angle study performed using the DeLouise Lab’s Rame-Hart contact angle measurement tool.   The entire study was performed on 8/1/06-8/10/06. Observations: Contact angles of non-plasma oxidized samples start ~60 degrees and increase over about 10 hrs

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Material changes

There’s been a flurry of activity regarding Jess’ recent discoloration post.  Specifically, there is a discussion about the recent materials changes that have taken place due to the rebuilt CVC sputterer.  This post is meant to supplement the ongoing materials

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Diffusion Separations w/ 670, 673

Wafers 670 and 673 were made to have different cutoffs. I set up diffusion experiments with two chips from each wafer using protein standards. However after removing samples after 24 hours I noticed that both chips from w670 had fully

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Pore processing influence on permeability results

I mostly finished re-processing the images with new method of using pore processor. The images of molar flow/porosity dependence with older and newer processed data are below. Older image: New image: They don’t look much different. Also you can not

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Negative Assay Follow Up

In yesterday’s post I showed that I was able to obtain good negative adsorption assay results, but there was one major problem. The cellulose and PES actually had higher protein concentrations after the assay. I suggested this was because they

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Negative Adsorption Assay

The Tecan Nanoquant plate is amazing.  For those of you who are unaware, we were able to demo a quartz plate that enabled absorbance measurements with only 2ul drops.  It took a little bit for me to figure it out,

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Tecan sensitivity

I did a quick experiment in order to show everyone what the Tecan allows us to do.  I made a dilution curve of rhodamine 6G in PBS and measured the absorbance and fluorescence with the fluorimeter. I first did an

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BSA detection on NC

Creating an array to hold a pnc-Si wafer to proving to be difficult. The PDMS spreads too rapidly though the NC to form a consistent array for the pnc-Si membrane (and eventually wafer) to rest on. I’m still running different

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Membranes with movable cutoff

Last week, we created a series of wafers that were RTPed at four different temperatures between 900 C and 1000 C.  Below is a comparison of the 900 C (left) vs. 1000 C RTP (right) wafer. We see that a

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