heavy walls, giving it mechanical strength, while retaining reasonable heat resistance. And, it is a glass that can be fabricated more easily than most other glasses, thus making it more economical.
Chemical Composition Composition (percent approx.)
Physical Properties
SiO2 |
81% |
B2O3 |
13.0% |
Na2O / K2O |
4.0% |
A12O3 |
2% |
Coeff. of Exp. |
32.5 x 10-7 cm/cm/°C |
Strain Point |
515°C |
Anneal Point |
565°C |
Soften Point |
820°C |
Density |
2.23 g/cm3 |
Temp. Limits |
490°C (Extreme Service) |
230°C (Normal Service) |
|
Max. Thermal |
Shock 160°C |
Applications
Designed for use in all products requiring very high resistance to strong acids, alkalis and products intended for use in heat applications such as autoclaves, hot plates and open flame.
Warnings
1. Thick-walled ware, such as bottles, jars and desiccators, should not be heated over a flame, a hot plate, or other comparable source of heat.
When chromic acid solution is used the item may be rinsed with the cleaning solution or it may be filled and allowed to stand.
The length of time it is allowed to stand depends on the amount of contamination on the glassware. Relatively clean glassware may require only a few minutes of exposure; if debris is present, such as blood clots, it may be necessary to let the glassware stand all night. Due to the intense corrosive action of the chromic acid solution, it is good practice to place the stock bottle, as well as the glassware being treated, in flat glass pans or pans made from lead or coated with lead, or plastic polymer pans determined compatible with the concentration of chromic acid you are using. Extra care must be taken to be sure chromic acid solution is disposed of properly. Special types of precipitates may require removal with nitric acid, aqua regia or fuming sulfuric acid. These are very corrosive substances and should be used only when required.
Removing Grease
Grease is best removed by boiling in a weak solution of sodium carbonate. Acetone or any other fat solvent may be used. Strong alkalis should not be used. Silicone grease is most easily removed by soaking the stopcock plug or barrel for 2 hours in warm decahydronaphthalene.
Drain and rinse with acetone or use fuming sulfuric acid for 30 minutes. Be sure to rinse off all of the cleaning agents.
Cleaning Glassware
Rinsing
It is imperative that all soap, detergents and other cleaning fluids be removed from glassware before use. This is especially important with the detergents, slight traces of which will interfere with serologic and cultural reactions.
After cleaning, rinse the glassware with running tap water. When test tubes, graduates, flasks and similar containers are rinsed with tap water, allow the water to run into and over them for a short time, then partly fill each piece with water, thoroughly shake and empty at least six times. Pipettes and burettes are best rinsed by attaching a piece of rubber tubing to the faucet and then attaching the delivery end of the pipettes or burettes to a hose, allowing the water to run through them. If the tap water is very hard, it is best to run it through a deionizer before using.
Rinse the glassware in a large bath of distilled water. Rinse with distilled water. To conserve distilled water, use a five gallon bottle as a reservoir. Store it on a shelf near your clean-up area. Attach a siphon to it and use it for replenishing the reservoir with used distilled water. For sensitive microbiologic assays, meticulous cleaning must be followed by rinsing 12 times in distilled water.
Sterilizing Contaminated Glassware
Glassware which is contaminated with blood clots, such as serology tubes, culture media, petri dishes, etc., must be sterilized before cleaning. It can best be processed in the laboratory by placing it in a large bucket or boiler filled with water, to which 1-2% soft soap or detergent has been added, and boiled for 30 minutes. The glassware can then be rinsed in tap water, scrubbed with detergent, rinsed again.
You may autoclave glassware or sterilize it in large steam ovens or similar apparatus. If viruses or spore- bearing bacteria are present, autoclaving is absolutely necessary.
Handling and Storing
To prevent breakage when rinsing or washing pipettes, cylinders or burettes, be careful not to let tips hit the sink or the water tap. Dry test tubes, culture tubes, flasks and other labware by hanging them on wooden pegs or placing them in baskets with their mouths downward and allowing them to dry in the air; or place them in baskets to dry in an oven. Drying temperatures should not exceed 140°C. Line the drying basket with a clean cloth to keep the vessel mouths clean.
Dry burettes, pipettes and cylinders by standing them on a folded towel. Protect clean glassware from dust. This is done best by plugging with cotton, corking, taping a heavy piece of paper over the mouth or placing the glassware in a dust-free cabinet. Store glassware in specially designed racks. Avoid breakage by keeping pieces separated.
Do not store alkaline liquids in volumetric flasks or burettes. Stoppers or stopcocks may stick.
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Glass Properties
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Glass Cleaning and Use