Sharra Grow Winterthur/University of Delaware Program in Art Conservation When New and Improved Becomes Outdated and Degraded: The Technical Study and Treatment of a 1964 Pop Art Painted Collage abstract



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Table 3. Scanning Electron Microscopy-Energy Dispersive Spectroscopy/Back Scattered Electron Imaging Results



Sample

Description

(cross section unless otherwise noted)



Results

(relevant elements in bold)



Colorants Inferred

S-G1

degraded green paint

C, O, Al, S, Cu, Zn, As, Cd

emerald green, cadmium yellow, zinc white

S-O1

orange paint layer

C, O, Mg, Al, Si, S, Se, Cd, Ba

cadmium orange or cadmium red lithopone, barium sulfate

white paint layer

C, O, Na, Mg, Al, Si, S, Cl, Ca, Ti

titanium white, calcium carbonate and/or calcium sulfate, alumino-silicate

S-S1

silver paint layer

Al

metallic aluminum

degraded green paint layer

C, O, Al, S, Cl, Cu, Zn, As, Cd

emerald green, cadmium yellow, zinc white

C1-ground

white ground layers

O, Na, Mg, Al, Si, S, Cl, K, Ca, Ti, Fe

titanium white, calcium sulfate, alumino silicates (possibly a clay extender)

S-DG1

dark green paint layer

Mg, Si, S, K, Ca, Ti, Cr, Fe, Zn, Cd

chromium oxide green, cadmium orange, titanium white

silver paint layer

Al

metallic aluminum

white paint layer

Mg, Al, Si, S, Cl, K, Ca, Ti, Fe, Cu, Ba

barium sulfate, alumino-silicate

S-B4

black paint layer

O, Na, Mg, Si, P, S, Cl, K, Ca, Fe

possibly bone black

silver paint layer

Al

metallic aluminum

white paint layer

C, O, Ti, Na, Mg, Si, S, Cl, Ca, Fe,

titanium white (possibly calcium sulfate, anhydrite)

Paper

brown paper sample, un-mounted

C, O, Na, Al, Si, S, Ca, Ti

alumino-silicates (clay), calcium carbonate, titanium white

Table 4. Information on filter cubes and fluorescent stains used during cross-sectional analysis



Microscope filter cubes used on the sample cross sections:

Blue Excitation: Nikon B-2A (ex. 450-490 nm, ba 520 nm)

Green Excitation: Nikon G-1B (ex. 546/10 nm, ba 590 nm)

Violet Excitation: Nikon BV-2A (ex 400-440 nm, ba 470nm)



Fluorescent stains used on the sample cross sections:

TTC (Triphenyl Tetrazolium chloride) with a concentration of 4.0% in anhydrous methanol (0.2g/5ml). Stains for Carbohydrates, reducing sugars, reducing compounds. Positive reading is red/brown using the UV-2A filter cube.


488 (Alexa Fluor 488) with a concentration of 0.02% in water (pH 9), 0.05%M borate and 5% DMF solution. Stains for proteins. Positive reading is yellow/yellow-green using the B-2A filter cube.

FITC (Fluorescein isothiocyanate) with a concentration of 0.2% in anhydrous acetone (0.01g/5ml). Stains for free amino containing groups (proteins). Positive reading is yellow/green using the B-2A filter cube.


FITC conjugated lyophilized powder with a concentration of 1% in water (pH 9), 0.05%M borate. Stains for chitin (mold). Positive reading is yellow/green using the B-2A filter cube.
DCF (2,7, Dichlorofluorescein) with a concentration of 0.02% in ethanol. Stains for saturated and unsaturated lipids (oils). Positive reading is pink for saturated lipids and yellow for unsaturated lipids using the B-2A filter cube.
RHOB (Rhodamine B) with a concentration of 0.06% in ethanol or 1:1 ethanol:xylene (0.003g/5ml). Stains for lipids (oils). Positive reading is red/orange using the G-1B filter cube.

XRF Sample Locations




SEM and Cross Section Sample Locations




GC/MS and FTIR Sample Locations







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