Spectrophotometric determination of the end groups of benzoic acid in polycaproamide

1980 ◽  
Vol 11 (4) ◽  
pp. 339-341
Author(s):  
L. P. Bakhmach ◽  
Z. S. Lapkina
Keyword(s):  
Benzoic Acid ◽  
Spectrophotometric Determination ◽  
End Groups

Spectrophotometric Determination of Some Preservatives in Milk

1977 ◽  
Vol 60 (5) ◽  
pp. 1175-1179
Author(s):  
Abdel-Aziz M Wahbi ◽  
Hassan Abdine ◽  
Salah M Blaih
Keyword(s):  
Benzoic Acid ◽  
Absorption Spectra ◽  
Spectrophotometric Determination ◽  
Sorbic Acid ◽  
Percentage Error ◽  
Milk Samples ◽  
First Derivative

Abstract Benzoic acid, propyl p-hydroxybenzoate, and sorbic acid in milk have been determined by using the corresponding first derivative curves of absorption spectra of clarified milk samples. The ΔA/Δλ curves were computed and the concentration of each preservative was calculated using 1 point, 2 points, and/or 3 points. In all cases, the percentage error was within 2.4%.

scholarly journals Spectrophotometric Determination of Palladium(II) Ions Using a New Reagent: 4-(N’-(4-Imino-2-oxo-thiazolidine-5-ylidene)-hydrazino)-benzoic Acid (p-ITYBA)

2020 ◽  
Vol 2020 ◽  
pp. 1-8 ◽  
Author(s):  
Oleksandr S. Tymoshuk ◽  
Orest S. Fedyshyn ◽  
Lesia V. Oleksiv ◽  
Petro V. Rydchuk ◽  
Vasyl S. Matiychuk
Keyword(s):  
Detection Limit ◽  
Complex Formation ◽  
Benzoic Acid ◽  
Spectrophotometric Determination ◽  
Spectrophotometric Method ◽  
Molar Absorptivity ◽  
Water Medium ◽  
Analytical Reagent ◽  
Optimal Ph

The simple, rapid spectrophotometric method for palladium(II) ions determination using a new analytical reagent is described. The interaction of Pd(II) ions with a reagent, of the class of azolidones, 4-(N′-(4-imino-2-oxo-thiazolidine-5-ylidene)-hydrazino)-benzoic acid, in water medium results in the formation of a complex. The Pd(II)-p-ITYBA complex shows maximum absorbance at a wavelength of 450 nm. The molar absorptivity is 4.30 × 103 L·mol−1·cm−1. The optimal pH for complex formation is 7.0. The developed method has a wide linearity range of 0.64–10.64 µg·mL−1 for Pd(II). The detection limit is 0.23 µg·mL−1. It was found that Co(II), Ni(II), Zn(II), Fe(III), Cu(II), Al(III), and many anions do not interfere with the Pd(II) determination. The proposed method was tested in the analysis of model solutions and successfully applied for the determination of palladium in catalyst. The obtained results show that this method can be used for serial determinations of palladium in various objects.

Enzymic Method for the Spectrophotometric Determination of Benzoic Acid in Soy Sauce and Pickles

The Analyst ◽  
1997 ◽  
Vol 122 (3) ◽  
pp. 259-262 ◽  
Author(s):  
Takashi Hamano ◽  
Yukimasa Mitsuhashi ◽  
Nobumi Aoki ◽  
Masanori Semma ◽  
Yoshio Ito
Keyword(s):  
Benzoic Acid ◽  
Spectrophotometric Determination ◽  
Soy Sauce

scholarly journals Investigation of Charge Transfer Complex Formation Between Fe(III) and 2,6-Dihydroxy Benzoic Acid and its Applications for Spectrophotometric Determination of Iron in Aqueous Media

2009 ◽  
Vol 6 (4) ◽  
pp. 985-992 ◽  
Author(s):  
Mohammad Saeid Hosseini ◽  
Sara Madarshahian
Keyword(s):  
Charge Transfer ◽  
Stability Constant ◽  
Benzoic Acid ◽  
Spectrophotometric Determination ◽  
Dynamic Range ◽  
Charge Transfer Complex ◽  
Aqueous Media ◽  
Acidic Media ◽  
Relative Standard

On the basis of affinity of Fe(III) ions toward functional groups of 2,6-dihydroxy benzoic acid (2,6-DHB), a charge transfer complex (CT) is formed between Fe(III) ion and 2,6-DHB in acidic media. The stoichiometry and stability constant of the complex was determined using both mole ratio and Job’s methods. The stability constant of 1:1 complex formed in acidic media is 2.55±0.14×105(mole ratio) or 2.70±0.12×105(Job), in which the quantities are in agreement with together. This method was used for spectrophotometric determination of Fe(III) in aqueous media. The dynamic range and detection limit (DL) were 1.2×10-5to 3.6×10-4M and 1.5×10-6M, respectively. The relative standard deviation (RSD) was found to be 0.76% in the replicate treatments (n=7) with 1.6×10-4M Fe(III). The practical applicability of the method was confirmed using a synthetic certificated reference material (CRM) and spiked natural water samples.

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