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<t>FT-IR</t> spectrum of Ba 2 Mg(BO 3 ) 2 indicating characteristic vibrational bands.
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<t>FT-IR</t> spectrum of Ba 2 Mg(BO 3 ) 2 indicating characteristic vibrational bands.
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Structural characteristics of MSYs supplemented with API. (A) Focused ion beam scanning electron microscopy images at 100× and 200× magnification, <t>(B)</t> <t>FT-IR</t> spectra, (C) protein secondary structure composition, (D) ζ-potential, and (E) free sulfhydryl content before and after fermentation. A0: MSY without API, A0.5: MSY supplemented with API 0.5%, A1: MSY supplemented with API 1%, A1.5: MSY supplemented with API 1.5%, A2: MSY supplemented with API 2%. For (D), a–e indicate significant differences among formulations ( p < 0.05). For (E), A–E and a–e indicate significant differences among formulations before and after fermentation, respectively ( p < 0.05). ⁎ , ⁎⁎ , and ⁎⁎⁎ indicate significant differences before and after fermentation within each formulation at p < 0.05, p < 0.01, and p < 0.001, respectively.
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Structural characteristics of MSYs supplemented with API. (A) Focused ion beam scanning electron microscopy images at 100× and 200× magnification, <t>(B)</t> <t>FT-IR</t> spectra, (C) protein secondary structure composition, (D) ζ-potential, and (E) free sulfhydryl content before and after fermentation. A0: MSY without API, A0.5: MSY supplemented with API 0.5%, A1: MSY supplemented with API 1%, A1.5: MSY supplemented with API 1.5%, A2: MSY supplemented with API 2%. For (D), a–e indicate significant differences among formulations ( p < 0.05). For (E), A–E and a–e indicate significant differences among formulations before and after fermentation, respectively ( p < 0.05). ⁎ , ⁎⁎ , and ⁎⁎⁎ indicate significant differences before and after fermentation within each formulation at p < 0.05, p < 0.01, and p < 0.001, respectively.
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Structural characteristics of MSYs supplemented with API. (A) Focused ion beam scanning electron microscopy images at 100× and 200× magnification, <t>(B)</t> <t>FT-IR</t> spectra, (C) protein secondary structure composition, (D) ζ-potential, and (E) free sulfhydryl content before and after fermentation. A0: MSY without API, A0.5: MSY supplemented with API 0.5%, A1: MSY supplemented with API 1%, A1.5: MSY supplemented with API 1.5%, A2: MSY supplemented with API 2%. For (D), a–e indicate significant differences among formulations ( p < 0.05). For (E), A–E and a–e indicate significant differences among formulations before and after fermentation, respectively ( p < 0.05). ⁎ , ⁎⁎ , and ⁎⁎⁎ indicate significant differences before and after fermentation within each formulation at p < 0.05, p < 0.01, and p < 0.001, respectively.
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Structural characteristics of MSYs supplemented with API. (A) Focused ion beam scanning electron microscopy images at 100× and 200× magnification, <t>(B)</t> <t>FT-IR</t> spectra, (C) protein secondary structure composition, (D) ζ-potential, and (E) free sulfhydryl content before and after fermentation. A0: MSY without API, A0.5: MSY supplemented with API 0.5%, A1: MSY supplemented with API 1%, A1.5: MSY supplemented with API 1.5%, A2: MSY supplemented with API 2%. For (D), a–e indicate significant differences among formulations ( p < 0.05). For (E), A–E and a–e indicate significant differences among formulations before and after fermentation, respectively ( p < 0.05). ⁎ , ⁎⁎ , and ⁎⁎⁎ indicate significant differences before and after fermentation within each formulation at p < 0.05, p < 0.01, and p < 0.001, respectively.
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FT-IR spectrum of Ba 2 Mg(BO 3 ) 2 indicating characteristic vibrational bands.

Journal: RSC Advances

Article Title: Adsorption of crystal violet and malachite green onto dibarium magnesium orthoborate (Ba 2 Mg(BO 3 ) 2 ): equilibrium, kinetics and thermodynamics

doi: 10.1039/d6ra03351b

Figure Lengend Snippet: FT-IR spectrum of Ba 2 Mg(BO 3 ) 2 indicating characteristic vibrational bands.

Article Snippet: Fourier Transform Infrared (FT-IR) spectroscopy of Ba 2 Mg(BO 3 ) 2 was performed using a JASCO FT/IR-4700 Type A instrument to identify functional groups present in the material.

Techniques:

Structural characteristics of MSYs supplemented with API. (A) Focused ion beam scanning electron microscopy images at 100× and 200× magnification, (B) FT-IR spectra, (C) protein secondary structure composition, (D) ζ-potential, and (E) free sulfhydryl content before and after fermentation. A0: MSY without API, A0.5: MSY supplemented with API 0.5%, A1: MSY supplemented with API 1%, A1.5: MSY supplemented with API 1.5%, A2: MSY supplemented with API 2%. For (D), a–e indicate significant differences among formulations ( p < 0.05). For (E), A–E and a–e indicate significant differences among formulations before and after fermentation, respectively ( p < 0.05). ⁎ , ⁎⁎ , and ⁎⁎⁎ indicate significant differences before and after fermentation within each formulation at p < 0.05, p < 0.01, and p < 0.001, respectively.

Journal: Food Chemistry: X

Article Title: Modulating protein–polysaccharide gel networks via almond protein to improve physicochemical stability of millet-based set yogurt

doi: 10.1016/j.fochx.2026.104535

Figure Lengend Snippet: Structural characteristics of MSYs supplemented with API. (A) Focused ion beam scanning electron microscopy images at 100× and 200× magnification, (B) FT-IR spectra, (C) protein secondary structure composition, (D) ζ-potential, and (E) free sulfhydryl content before and after fermentation. A0: MSY without API, A0.5: MSY supplemented with API 0.5%, A1: MSY supplemented with API 1%, A1.5: MSY supplemented with API 1.5%, A2: MSY supplemented with API 2%. For (D), a–e indicate significant differences among formulations ( p < 0.05). For (E), A–E and a–e indicate significant differences among formulations before and after fermentation, respectively ( p < 0.05). ⁎ , ⁎⁎ , and ⁎⁎⁎ indicate significant differences before and after fermentation within each formulation at p < 0.05, p < 0.01, and p < 0.001, respectively.

Article Snippet: FT-IR spectra of the lyophilized MSYs and native API were obtained using an FT-IR spectrophotometer (FT/IR-4100 type A, JASCO, Tokyo, Japan).

Techniques: Scanning Electron Microscopy, Formulation