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Effects of gel depth and gel surface area on agar gel strength

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Date
1993
Author
de Castro, Teresa R.
Page views
2,914
ASFA keyword
agar ASFA
colloids ASFA
gels ASFA
seaweed products ASFA
AGROVOC keyword
Rhodophyta AGROVOC
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Abstract
Agar is a high priced phycocolloid extracted from red seaweeds (Rhodophyta) called agarophytes. It is a mixture of polysaccharides whose basic monomer is galactose (Armisen and Galatas 1987). Agar has many uses in the food and pharmaceutical industry, and the measure of its commercial value is based on its physical properties. One of the most important physical properties of commercial agar products is its gel strength (Chandrkrachang and Chinadit 1988). Gel strength is the force required to rupture the gel and it is measured through the use of gel testers available in the market, such as the Nikkan-sui, Rowerbal, and the Marine Colloids gel testers. Each instrument has built-in specifications for optimum use and results. Standard procedures used in the preparation of 1.5% agar gels for gel strength determination usually require 1.5 g of sample. Replication of samples in laboratory testing is however standard requirement and replication is constrained when sample extracts are scarce.

This paper discusses the effects on gel strength of different gel depths and gel surface areas. It aims to identify the minimum size of vessel and depth of gel that will give optimum results using a Marine Colloids Model GT-2 gel tester.
URI
http://hdl.handle.net/10862/1411
Suggested Citation
de Castro, T. R. (1993). Effects of gel depth and gel surface area on agar gel strength. The Philippine Scientist, 30, 100-103. http://hdl.handle.net/10862/1411
Type
Article
ISSN
0079-1466
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  • Journal Articles [1266]

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    Seasonality of yield and gel strength of agar from Gracilaria heteroclada was determined. Gel strength was high (510-794 gm cm-2) during early dry season (October-March) and low (43-101 gm cm-2) during the wet season (May-August). A negative correlation exist (P ≤ 0.05) between agar yield and gel-strength.
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    Agar production from Gracilariopsis heteroclada (Gracilariales, Rhodophyta) grown at different salinity levels 

    Hurtado-Ponce, A. Q. (Walter de Gruyter, 1994)
    Gracilariopsis heteroclada grown in fiber glass tanks at four salinity levels was treated with three different concentrations of aqueous NaOH. Yield, gel strength, gelling and melting temperatures of the extracted agar were determined. Plants grown at salinities of 24 and 32 ppt and treated with 3% NaOH produced the strongest gel (850 g cm-2) and weakest gel (300 g cm-2), respectively. Statistically significant differences in gel strength, dynamic gelling and melting temperatures were observed between the various treatments. The interactive effect of salinity and NaOH was significant in gel strength, gelling and melting temperatures of the gel from G. heteroclada.
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    Evaluation of agar from three species of Gracilaria from Panay and Guimaras islands 

    de Castro, Teresa R. (San Carlos Publications, University of San Carlos, 1993)
    Agar from three species of Gracilaria, G. changii G. coronopifolia, and Gracilariopsis heteroclada, collected form Panay and Guimaras islands was evaluated. Each species was pretreated with NaOH solution before extraction. Highest agar yields were obtained following alkaline pretreatment at the lowest concentration (1% NaOH) for all species. Highest gel strengths were obtained at different alkaline pretreatment conditions: 644 ± 3.4 g cm-2 at 3 % NaOH for 60 min for G. changii, 641 ± 11.9 g cm-2 at 5 % NaOH for 30 min for G. heteroclada, and 170 g cm-2 at 5 % NaOH for 30 min G. coronopifolia. Agar gelling temperatures ranged from 38.5-40ºC and agar melting temperature ranged from 80.5-85 ºC. Specific viscosity was highest for agar from G. changii at 18 cps. Moisture and ash contents ranged from 8.04-15.20 % and 4.32-4.98%, respectively. Based on the result for this study, G. heteroclada and G. changii are two species which merit further studies for their prospective commercial value to the different industries using agar.

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