Crab-shell chitin (SC-20) was evaluated for its ability to enhance biological denitrification in bench-scale tests. In the presence of SC-20, highly reducing conditions were generated, supporting both denitrification and sulfate reduction of aerated water. Rapid degradation of protein in SC-20 was observed to cause an initial high release of ammonium and carbon, while a slower, continuous release of calcium carbonate from the crab shell maintained the pH near 9 throughout the tests. In batch tests, denitrification rates of 2.4+/-0.2 mg N/L-d were obtained. Columns receiving a continuous nitrate load of 24.5 mg N/L-d sustained complete denitrification for an average of 149 d (250 pore volumes). The denitrification rates and longevity of SC-20 chitin are comparable to, or better than, those previously reported for other polymeric substrates. This, in addition to its particle size, non-swelling nature, and ease of delivery in slurry form make SC-20 an attractive electron donor source for groundwater bio-denitrification.
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http://dx.doi.org/10.1016/j.biortech.2008.06.052 | DOI Listing |
Curr Res Microb Sci
November 2024
Department of Biotechnology, Utkal University, Vani Vihar, Bhubaneswar 751004, Odisha, India.
Chitosan is a promising biopolymer with wide range of applications. It is the deacetylated product of chitin. Commercially, it is produced from chitin via a harsh thermochemical process that has several shortcomings and heterogenous deacetylation product.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
PG & Research Department of Physics, Sree Sevugan Annamalai College, (Affiliated to Alagappa University, Karaikudi), Devakottai 630 303, Tamil Nadu, India. Electronic address:
For biomedical applications, material scientists all over the world are working to develop cost-effective technologies and thereby synthesize new nanocomposite materials that are biocompatible, bioactive, scalable and naturally abundant. This study focuses on synthesizing and evaluating nanocomposites of zinc oxide (ZnO) and chitosan (CS) derived from crab shells, in three different weight proportions (1:0.5, 1:1, and 1:2).
View Article and Find Full Text PDFFoods
August 2024
Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL A1C 5S7, Canada.
The snow/pink crab () and Northern shrimp () are widely distributed in the North Atlantic Ocean. During processing/consumption, about 80% of the harvest is discarded as processing waste, which is a rich source of protein, chitin, minerals, and carotenoids. This study, for the first time, investigated the proximate composition and individual amino acids, minerals, and carotenoids from different body parts (carapace, shoulder, claw, tip, and leg) of snow crabs and shrimp shells.
View Article and Find Full Text PDFCarbohydr Polym
December 2024
Department of Molecular Sciences and Nanosystems, Università Ca' Foscari di Venezia, 30172 Venezia Mestre, Italy. Electronic address:
A green protocol to extract chitin from crab shells using water soluble ionic liquids (ILs) is here reported. Compared to conventional multistep acid-base extraction methods, this one-pot procedure achieves pulping of recalcitrant crustacean waste shells by employing ammonium acetate, ammonium formate and hydroxylammonium acetate as water-soluble, low-cost and easy to prepare ILs. An extensive parametric analysis of the pulping process has been carried out with different ILs, different ratios, temperature and time.
View Article and Find Full Text PDFInt J Biol Macromol
May 2024
Department of Life Sciences, Gachon University, Seongnamdaero 1342, Seongnam-si, Gyeonggi-do 461-701, Republic of Korea. Electronic address:
This investigation aimed to scrutinize the chemical and structural analogies between chitosan extracted from crab exoskeleton (High Molecular Weight Chitosan, HMWC) and chitosan obtained from mushrooms (Mushroom-derived Chitosan, MRC), and to assess their biological functionalities. The resulting hydrolysates from the hydrolysis of HMWC by chitosanase were categorized as chitosan oligosaccharides (csCOS), while those from MRC were denoted as mrCOS. The molecular weights (MW) of csCOS and mrCOS were determined using Matrix-Assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF) mass spectrometry.
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