Overview
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Key numbers
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- reduction of mercury in canned Albacore tuna by 25–35%, depending on the late, methylmercury remains a pressing
- water-based sauces. Thiolated silica was chosen due to strong in the solution keeping 80 wt% of the solution and as prepared
- veloped approach involves utilizing a simple, single-component umes (10–80 wt%) of the extracting solution and the variations in
- known and efficient mercury-binding agent (which is explained range between 1 to 12 h was also conducted. In this case, the fish
- component responsible for mercury capturing. Various param- tracting solution (1.2 wt% of cysteine) the samples were stored at
- glass jar and filled with the extracting solution (1.2 wt% of cys-
- European reference material of fish muscles ERM-BB422 with teine) keeping the 60 wt% of the solution in each sample. Then,
- was suspended in 0.5 m solution of NaOH for 1 h at room temper- obtained by storage of canned tuna in the 1.2 wt% solution of
-
- reading was assessed using certified fish protein standard to the minced sample. Nevertheless, a 36% reduction of mercury
- the average result was equal to 0.602 ± 0.031 mg kg−1 . S1b, Supporting Information). The 3–4% higher mercury extrac-
- capacity of mercury scavenging from the fish tissue. The effect of tive concentration of cysteine was found to be 1.2 wt% for both
- cysteine concentration on mercury extraction from four kinds of samples of canned fish, and 1.6 wt% in the case of fish protein
- lutions (80 wt% liquid content) for 1 h is presented in Figure 2. 3.2. Effect of Time and Extracting Solution Content
- centage of the removed mercury was between 71 and 13%. The possible efficiency. In this view, the duration and the working
- bacore tuna, packed it in jars containing 60 wt% of the 1.2 wt%
- core tuna using different volumes of the 1.2 wt% cysteine solution for 1 h. finding since in the case of preserved products storage time does
- content of 80 wt% used in our previous experiments was rela- cysteine had a chance to reach deeper trapped mercury. Another
- content in water-canned tuna is typically ca. 25–30 wt% based on sarcoplasmic proteins which is possible at the pH of the applied
- 8% for the level of 30% solution content. For the whole pieces pacity of methylmercury adsorption from the water solution onto
- of canned tuna, 45% solution content in the sample has been the base material—silica 6 h reached the level of about 100 mg
- extraction mechanism is schematically presented in Figure 4. and 1.2%. The results are presented in Figure 6a as the relation-
- teine solution (80 wt% of solution content, logarithmic scale of totally prevented the adsorption process. That was an expected re-
- 13% of mercury extraction yield was reached after 50 min, and tween mercury and sulfur-containing proteins are strong enough
- no changes were observed up to 4 h of storage. Then a rapid to keep mercury stable in the solution, thereby hindering the ad-
- positive effects. Mercury adsorption by silica 6 h raised from 0% However, a direct comparison of the results for silica 24 h (hydr)
- to 7% which is still a very low level. The next step was to look for presented in Figure 6b for canned tuna and Figure 6c for fresh
- removal level was 33% (silica 24 (hydr)). Two single-point adsorp- mercury stabilization or by directly affecting the adsorbent
- Figure 5. Time dependence of mercury extraction from a) whole canned tuna using 1.2 wt% cysteine solution, 80% of the solution, no pH adjustments
- (initial pH = 5.2); b) fresh tuna after precooking and pasteurization—black curve (1.2 wt%, no pH adjustment, 60% of solution), adsorption of Hg from
- silica 6 h). b) Adsorption of mercury from the extract obtained from a whole canned fish with the solution containing 1.2 wt% cysteine using different
- The results are presented in Table 1. Based on the results, it A new simple method for the removal of mercury from tuna
- like EDTA and citric acid do not exhibit this behavior. However, of 1.2 wt% cysteine solution enabled the reduction of mercury
- some experiments in the laboratory of the authors of this paper content in canned albacore tuna meat by 35% and its transfer
- Table 1. Mercury adsorption from the model solutions prepared according to the representative cases from the literature (Initial concentration
- Cys (g L−1 ) EDTA (g L−1 ) Citric acid (g L−1 ) NaCl (g L−1 ) % Hg removed % of Hg extraction Refs.
- 30%. However, research on more powerful materials effectively (accessed: June 2024).
- tuna at least by 30% by simply separating the medium from (8) Q. Nong, H. Dong, Y. Liu, L. Liu, B. He, Y. Huang f, J. Jiang g, T. Luan,
Methods (brief)
- tively reduce the methylmercury level in fish meat during the Then, the samples of fish including the whole pieces of fresh and
- evidence regarding the successful application of sulfur-modified samples were stored at room temperature for 1 h. Mercury con-
- The study proposes a potentially straightforward and applica- above-described experiment. In this case, the samples of whole
- component responsible for mercury capturing. Various param- tracting solution (1.2 wt% of cysteine) the samples were stored at
- were investigated to ascertain the most optimal conditions for tion was determined by Hg analysis in the fish samples collected
- moving the collected mercury via the adsorption process using in the extracting solutions was conducted. This was to mimic the
- European reference material of fish muscles ERM-BB422 with teine) keeping the 60 wt% of the solution in each sample. Then,
- a certified mercury content of 0.601 ± 0.030 mg kg−1 was pur- the samples were pasteurized to avoid spoilage and enable their
- defined storage time (1–9 weeks), the samples were collected, the and called silica 24 h (hydr).
- at 105 °C, and then the desiccated material was placed in a plastic volume and adsorbent mass. The as-prepared samples were then
- conducted at 50 °C for 60 min, using a water bath shaker. Follow- ing a direct mercury analyzer (DMA-80 Direct Mercury Analysis
- cysteine. For this purpose, the collected extract samples were ex-
- Mercury analysis in the fish samples was conducted as follows:
- process was repeated. The as-obtained samples were subjected to
- comparison of the control samples that had no contact with any itating effective contact between the material and the solution.
- additional solutions. Generally, five types of fish samples were ex- Moreover, when the fish material is completely dry, it efficiently
- core tuna canned in water sauce, fresh tuna steak, and fresh tuna the sample. Tests were furthermore done with real samples, first
- sis, fish samples were freeze-dried with a Labcono FreeZone tray efficiency was lower in comparison to the powdered proteins be-
Implications
This page makes the source discoverable for category-level evidence routing. Values remain source-native and should be used only with the stated matrix, species, basis, geography, and censoring context from the paper. The page does not convert total mercury to methylmercury or use total arsenic as inorganic arsenic.
Wiki pages this source may touch
- Canned seafood (with tin flag)
- Fish — marine, predatory (tuna, swordfish, shark, king mackerel)
- Fish — marine, non-predatory (sardines, anchovies, salmon, cod)
- Mercury
- Mercury
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Update history
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