Examples of 'polymer of example' in a sentence
Meaning of "polymer of example"
Polymer of example describes a specific instance or representation of a polymer, which is a large molecule composed of repeating subunits. It implies that this specific case serves as an illustrative or representative example of the broader concept of polymers
How to use "polymer of example" in a sentence
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polymer of example
Optimum polycondensation conditions were determined for the polymer of Example III.
Polymer of Example.
A zinc object was coated with the polymer of example 1.
The polymer of example 5o showed wash persistence at least up to 5 shampoo washes.
A similar composition is prepared with the polymer of example 5.
By this procedure, the polymer of Example 8 was obtained in microporous form as flat disks.
Some devices were coated at this stage with the polymer of example 3.
The hold of the polymer of Example 1 is better than that of the comparative example.
Molecularly imprinted polymer of example 1.
The living PS. DVB polymer of Example 1 was employed as multifunctional initiator of anionic polymerization.
This polymer has similar properties as those described for the polymer of example 1.
The in vivo biodegradation of the polymer of Example 1 was determined over a four week period.
Study of the electrochemical behaviour of the polymer of Example 3.
EXAMPLE 4 The polymer of Example 2 was compounded and cured in a golf ball core formulation.
Films were prepared using the polymer of Example 2.
See also
The carbamate-functional polymer of Example E is a comparative polymer prepared by non-living radical polymerization.
The resulting polymer was as excellent in performance as the polymer of Example 4.
The polymer of the second metal-loaded polymer of Example 8 loaded with lanthanum and aluminum.
The studied gel is the gel comprising an absorbent polymer of Example 6.
The hydroxyl-functional polymer of Example A is a comparative polymer prepared by non-living radical polymerization.
A detergent formulation incorporating the polymer of Example 1 was also prepared.
The polymer of example 10 differs only from that of example 13 by its polymerization degree.
The specific extrusion conditions for the polymer of Example 4 are shown in Table 8a.
Example 8 The polymer of example 4 was used to coat arterial filter devices.
The polypropylene which was obtained was morphologically equivalent with the polymer of Example 1.
The carboxylic acid functional polymer of Example A is a comparative polymer prepared by non-living radical polymerization.
Thus substantial savings in line cost can be achieved when using the polymer of Example 1.
For blow moulding tests, the polymer of example 4 was produced.
FIG . 2 presents a plot of the molecular weight distribution of the polymer of Example 5.
By the same method, foams of polymer of example 7 can be produced.
FIG . 18 presents a plot of the short chain branching distribution of the polymer of Example 4.
G / dL solution of the polymer of Example 7 was prepared in methylene chloride.
Type 2 film properties an Collin laboratory line Polymer of Example.
The epoxy-reactive polymer of Example 7 was utilized to prepare the dispersion of Example 16.
One test blend contained the multiple function polymer of Example 1 and the other did not.
For instance, the polymer of Example 8 may be prepared utilizing the following process conditions,.
Similar composition is also prepared using the polymer of example 2 or 3 or 4.
The polymer of Example 32.5 had a broad molecular weight distribution as determined by gel permeation chromatography.
Inventive film 1 was made from a sample of the polymer of Example 2c.
The polymer of Example 4 was a substantially linear ethylene/1-butene copolymer prepared in a single solution polymerization reactor.
Inventive coating 1 was made from a sample of the polymer of Example 2c.
Antisoiling polymer of Example 2.
The polymer of Example 9 should be compared first with Comparative Example 2.
Example 8 utilizes the vinyl norbornene elastomeric polymer of Example 3 above.
Weight of polymer of Example 4.
The secondary extruder ( B ) melted and fed the sulfopolyester polymer of Example 8.
Then the olefin-carbon monoxide polymer of Example 4 was added and mixed.
Data The data in Tables 1-3 were generated utilizing the inverse emulsion polymer of Example 1.
The polymer of the first metal-loaded polymer of Example 8 loaded with palladium.
EXAMPLE 11, The polymer of Example 9 was obtained in an alternative microporous disc form.
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