Application of Gas-Liquid Microextraction (GLME)/GC-MS for Flavour and Fragrance in Ice Cream Detection and Composition Analysis
1
College of Food Science and Engineering, Changchun University, Changchun 130022, China
2
Jilin Province Product Quality Supervision and Inspection Institute, Changchun 130023, China
3
Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing 100081, China
*
Authors to whom correspondence should be addressed.
Molecules 2023, 28(2), 522; https://doi.org/10.3390/molecules28020522
Submission received: 15 November 2022
/
Revised: 28 December 2022
/
Accepted: 29 December 2022
/
Published: 5 January 2023
Abstract
:Under gas-liquid microextraction (GLME) operating conditions (extraction temperature 270 °C, extraction time 7 min, condensation temperature −2 °C, and carrier nitrogen gas speed 2.5 mL/min), ice cream samples, as a representative food, were pre-treated. The volatile aroma components of each sample was qualitatively analysed using GC-MS. The principal component analysis was conducted to classify the functional groups, which showed that alcohols, acids, esters, ketones, and aldehydes were the main compounds responsible for the aroma of ice cream. It was found that furan-3-carboxaldehyde, 3-furanmethanol, 2(5H)-furanone, 5-methylfuranal, 2,5-diformylfuran, 3-hydroxy-2-methyl-4-pyrone, 5-hydroxymethylfurfural, ethyl maltol, and glycerol were routinely used flavour ingredients in ice cream.
1. Introduction
With the rapid development of modern society, people are no longer just looking for satiety, health, and nutrition, but also have higher requirements for the flavour of food. The use of flavourings in food products can improve the diversity of food flavours, while aroma components are used as an index to judge the use of flavourings in foods. Due to the complex and unstable composition of volatile substances responsible for flavour, oxidation, polymerization, and condensation, reactions may occur during the extraction of volatile substances.
Flavours and fragrances are usually attached to complex food matrices, which also affect the composition analysis of flavours and fragrances [1,2]. Steam distillation [3,4], simultaneous distillation [5,6], static-headspace distillation [7,8,9], vacuum distillation [10], supercritical CO2 extraction [11,12], and solid-phase microextraction [13,14] techniques were widely used to extract volatile substances [15]. Each extraction method has its own advantages and disadvantages. Yang C et al. [16] used optimised gas-liquid microextraction parameters and detected alkylphenols in seafood by liquid chromatography. Nan et al. [17] used gas-liquid microextraction and gas chromatography-mass spectrometry to create a method for the rapid detection of multiple organophosphorus pesticide residues in edible mushrooms. Maltol and ethyl maltol are often added as food flavour enhancers in baked goods, ice cream, and maltol candy. In this experiment, gas-liquid microextraction (GLME)/GC-MS for food flavour and fragrance detection and composition analysis. The method is simple, quick, and reproducible, and only requires several milligrams for each analysis, which takes only a few minutes. Ethyl maltol as representative substance is used as general additive in ice cream, and the gas-liquid microextraction GLME /GC-MS detection method for flavour and fragrance is established.
Compared with other conventional additives, there are few systematic studies on the flavours and fragrances in food. The flavours and fragrances mentioned in China GB 2760-2014 and encoded in the Flavor and Extract Manufacturers Association (FEMA) of the United States are used as the principal component analysis and research, the principal component analysis of ice cream with a high use rate of flavours and fragrances were conducted through classification of functional groups.
2. Results and Discussion
2.1. Optimization of GLME Operating Conditions
2.1.1. Extraction Temperature
The ethyl maltol standard solution was pre-treated via GLME with extraction time of 7 min, carrier gas (Nitrogen) speed of 2.5 mL/min, and condensation temperature of −2 °C conditions were unchanged, samples were extracted at 240, 250, 260, 270, 280, and 290 °C, respectively. The detection progress was monitored according to the GLME working principle and operation conditions in Section 3.6. Through the GC-MS analysis, the influence of different extraction temperatures on the spiked recovery of ethyl maltol was investigated. As shown in Figure 1a, the spiked recovery rate was shown an increasing trend when the extraction temperature was within the gradient of 240 °C–270 °C, while the spiked recovery rate of the ethyl maltol standards were shown a decreasing trend when the extraction temperature was within the gradient of 270 °C–290 °C. This phenomenon of increasing temperature and decreasing spiked recovery rate is related to the structural changes of the ethyl maltol standards, which may have been accompanied by cleavage reactions or formation of isomers while the temperature is increasing, thus the optimal extraction temperature should be around 270 °C.
2.1.2. Extraction Time
Ethyl maltol standards were extracted at 5, 6, 7, 8, and 9 min, respectively, according to the GLME working principle and operation conditions in Section 3.6. Through GC-MS analysis, the influence of different extraction time on the spiked recovery rate of ethyl maltol samples were investigated. As shown in Figure 1b, the spiked recovery rate of ethyl maltol standard was shown that a slow increase in the extraction time from 5 min to 7 min; after 7 min, the spiked recovery rate tended to level off. It was indicated that when the extraction time was used as a single variable, after the extraction time reached a certain threshold value, too much extraction time would not have a great impact on the experiment. Thus, the optimal extraction time should be around 7 min.
2.1.3. Carrier Gas Speed
According to the GLME working principle and operation conditions in Section 3.6. Ethyl maltol standards were extracted by carrier gas speed at 1.0 mL/min, 1.5 mL/min, 2.0 mL/min, 2.5 mL/min, and 3.0 mL/min, respectively. As shown in Figure 1c, within practice operation, the spiked recovery rate of ethyl maltol sample was significantly improved when the carrier gas speed was in the gradient range of 1.0–2.5 mL/min. When the gas flow rate exceeds over 2.5 mL/min, the spiked recovery rate of ethyl maltol sample was decreases. It has been demonstrated that, although a fast gas flow rate can theoretically increase the contact area, too fast a gas flow rate in a confined space makes the purge state unstable and prevents the volatile components in the sample from being trapped by the purge in a stable manner.
2.1.4. Condensation Temperature
The condensation temperature was changed at −5 °C, −4 °C, −3 °C, −2 °C, −1 °C, and 0 °C, respectively, according to the GLME working principle and operation conditions in Section 3.6. The effect of different condensation temperatures on the spiked recovery rate of the ethyl maltol samples were investigated by GC-MS analysis, as shown in Figure 1d. It can be known that the influence of condensation temperature on the extraction progress of GLME was more significant. When the condensation temperature were increased from −5 °C to −2 °C, the spiked recovery rate of the samples tended to increase obviously, and when the condensation temperature was at −2 °C, the spiked recovery rate was at the highest value, when the condensation temperature continued to increase, the spiked recovery rate was decreased, which indicated that the condensation temperature needs to reach a certain level in order to complete the sample transformation from gas phase to liquid phase in order for the volatile substances extracted by GLME to be received back as much as possible; thus −2 °C was chosen as the optimal condensation temperature in this study.
2.1.5. Response Surface Design Optimization
Design Experts 12 was used to optimize the design by response surface design, and the spiked recovery rate of ethyl maltol sample was used as the response variable. The four factors, extraction temperature (A), extraction time (B), carrier gas speed (C), and condensation temperature (D), had a large effect on the spiked recovery rate of ethyl maltol, and the experimental data were designed and processed.
In order to find the optimal GLME extraction conditions for the ethyl maltol samples, a binary multiple regression equation was constructed for the four factors, extraction temperature (A), extraction time (B), carrier gas speed (C), and condensation temperature (D), with the spiked recovery rate (Y) of ethyl maltol samples, as shown in the following Equation (1):
In the regression equation fitted by the response surface model, a positive coefficient of the linear phase indicates that the factor acts synergistically on the response value, a positive correlation between the response value and the factor. Conversely, a linear phase with a negative coefficient indicates an antagonistic effect on the response value, a negative correlation between the response value and the factor. From the above equation, it was clearly seen that A, B, C, D, AC, BC, BD, and CD acted synergistically on the spiked recovery rate of ethyl maltol samples.
The analysis of variance (ANOVA) in Design Expert 12 is mainly used to verify the significance and generalizability of the regression equation for the experimental data (Table 1). A larger F-value proves that the fit is more significant, and, when the p-value is less than 0.05, it can prove the goodness of fit of the model. The interaction factors with p-values less than 0.05 have AC, BD and CD (Figure 2), when the stronger the interaction between the two factors, the more significant the effect on the response value, the more curved and steep the fitted response surface is, the more dense the contours are, and the more elliptical the shape tends to be. The response value R2 was 0.9898, which proves that the model of response surface simulation was more reliable, and the predicted accuracy of each parameter of GLME operating conditions was more reliable.
The optimal GLME operating conditions were optimized and obtained according to the actual situation, namely: extraction temperature of 270 °C, extraction time of 7 min, gas flow rate of 2.5 mL/min, and condensation temperature of −2 °C. The average yield of response value ethyl maltol spiked recovery rate was 78.90%, which was consistent with the optimized result of response value of 78.90%.
2.2. Principal Components(Pcs) Analysis of Ice Cream
2.2.1. GC-MS Analysis
Ten ice cream samples were analysed by GC-MS to contain components with ≥80% similarity (Table 2), and the chromatogram of samples were obtained. In Figure 3, a total of 85 volatile components were detected in 10 ice cream samples. The identified components were grouped according to functional groups and the classification results were as follows: 8 alcohols, 13 acids, 22 esters, 8 aldehydes, 15 ketones, 3 phenols, 11 heterocycles, 3 alkanes, 2 amines, and 1 ether. Among the identified components, esters accounted for the largest proportion (25.58%), followed by ketones (17.44%), and acids (15.12%). Ether accounted for the smallest proportion (1.16%) (Figure 4a).
2.2.2. Analysis of Volatile Aroma Components
Among the 85 volatile components identified in the 10 ice cream samples, 13 co-occurring components were detected, namely formic acid, acetic acid, glycerol, 3-furanomethanol, acetone alcohol, furan-3-carboxaldehyde, 5-methylfurfural, 5-hydroxymethylfurfural, 5-acetoxymethyl-2-furaldehyde, methyl maltol, methylcyclopentenolone, 2(5H)-furanone, and methyl furfurate. Among them, acetic acid and glycerine are generally used as flavourings and fragrances in food to add flavour to ice cream, and are also common ingredients in food processing. Additionally, 3-Furanmethanol is not codified by FEMA; however, according to the literature review, this substance has the aroma of roasted potatoes [18]. Additionally, 3-Furfural has a sweet aroma similar to fermented bread with charred aroma [19]. In addition, 5-Methyl furfural has a caramel rich sweet aroma [20], and the source of this aroma is mainly the Maillard reaction [21], 5-hydroxymethyl furfural has a sweet characteristic flavour similar to caramel or coffee, 5-acetoxymethyl-2-furaldehyde has a floral aroma [22], methyl maltol embodies a creamy caramel sweet aroma, methyl cyclopentenol ketone will embody the aroma of liquorice after dilution, which is allowed to be used in foods, such as creamy hard candy in China’s GB 2760-2014; 2(5H)-furanone has a fruity sweet aroma [23]. When used as a synthetic flavouring, methyl furoate will embody different aromas at different dilutions, possessing the flavour of caramel at low dilutions, and releasing a fruity aroma at high dilutions [24].
In addition, among the 10 samples studied, some components, such as 4-hydroxy-2,5-dimethyl-3(2H)furanone, (+)-limonene, and pineapple ester, were also detected in individual ice cream samples. Upon review, 4-hydroxy-2,5-dimethyl-3(2H)furanone can impart baking and caramel aromas to foods, (+)-limonene has citrus and lemon aromas, which was associated with the orange flavour of the samples, pineapple ester, as implied by the name, can add pineapple aroma to foods [25]; therefore, this component was detected in the pineapple flavoured samples.
Statistical analysis of principal components(PCs) was performed on the processed data by SPSS 23.0 software.
In principal component analysis, factor analysis can simplify complex multivariate factors by using as few factors as possible to analyse the influence of volatile aroma components in samples (Figure 4b and Figure 5). Before the factor analysis of volatile aroma components in ice cream samples, the content of phenols, alkanes, ethers, and amines in all components was low, therefore, the above four substances were removed from the factor analysis before analysis was performed. The characteristic roots and contribution rate (percent variance) of the principal components (PCs) in the ice cream sample were used as the basis for selecting the principal components (PCs). It can be observed that the contribution of characteristic roots greater than 1 come from the first three factors. Through the contribution rate was shown that the total variance of the first three factors reached 78.170%. That is, a three-factor model explained 78.170% of the entire analysed data.
The functional groups with high positive correlation in the first principal factor (PC1) were aldehydes and heterocycles in Figure 4b, while alcohols showed high negative correlation, esters and acids showed high positive correlation in the second principal factor(PC2), and ketones showed high positive correlation in the third principal factor(PC3). It can be further inferred from the total variance contribution of the first two principal factors above 50% in Figure 4. that aldehydes, esters, alcohols, acids, ketones, and heterocyclic groups were the characteristic functional group categories in the volatile aroma of ice cream.
2.3. Quantitative Analysis of Samples
According to Section 3.8, the quantitative results of functional groups detected in randomly selected ice cream were calculated. Statistical analysis was conducted on functional groups categories and concentrations of each sample, as shown in Figure 6.
It could be seen that the quantities of aldehydes were the largest in all detected functional groups. All samples contained aldehydes, such as furfural, furan-3-carboxaldehyde, 5-methylfurfural and 5-hydroxymethylfurfural, which give them a sweet caramel flavour. Esters mostly contribute to a fruity fragrance [26,27].
3. Materials and Methods
3.1. Experimental Materials and Reagents
Different flavours and manufacturers of ice cream were purchased from a retail market.
Methanol (chromatographic purity, 95%) was purchased from TEDIA Co., Ltd (Tedia Way Fairfield, OH, USA). Anhydrous sodium sulphate (analytical purity) was purchased from Sinopharm Chemical Reagent Co., Ltd (Shanghai, China). It was heated at 400 °C for 12 h, then cooled, and stored in a dryer before use. Quartz wool (Aoreilong New Materials Technology Co., Ltd. Shandong, China) was activated at 400 °C for 10 h before use. A C19 normal alkane standard solution (chromatographic purity, 99.9%) was purchased from Aladdin (Shanghai, China). Dichloromethane (chromatographic purity, 95%) was purchased from TEDIA Co., Ltd. (Tedia Way Fairfield, OH, USA) Ethyl maltol (purity, 99%)was purchased from J&K Scientific Co., Ltd. (Beijing, China).
3.2. Experimental Instruments
Gas-liquid microextraction (ME-101) developed by the Key Laboratory of Changbai Mountain Biological Resources and Functional Molecules, the Ministry of Education, Yanbian University (Figure 7). Gas chromatography-mass spectrometry (GC-MS-QP2010), Shimadzu (Tokyo, Japan) was used.
3.3. GC-MS Conditions
3.3.1. Gas Chromatography Conditions
GC was performed using a 0.25 µm, 30 m × 0.25 mm J and W DB-5 quartz capillary column. The heating procedure involved holding at 40 °C for 2 min, and increasing to 150 °C at 5 °C/min, then heating to 280 °C at 15 °C/min and holding for 5 min.
3.3.2. Mass Spectroscopy Conditions
The carrier gas was helium (He), purity ≥99.999%, with a flow rate of 1.78 mL/min. The injection volume was 1.0 µL. The injection mode was non-shunt injection. The ionization mode was electron bombardment (EI). The impact power was 70 eV. The GC-MS interface temperature was 300 °C. The ion source temperature was 230 °C. The full-scan mode was used, with a mass scan range of m/z 29–500, and a solvent delay of 2.5 min.
3.4. Sample Preparation
The ice cream were homogenized as samples by homogenizer, and numbered ice cream separately from 01 to 10; these samples were stored at −4 °C.
3.5. Preparation of Standard Solution
Ethyl maltol reserve solution was prepared by precisely weighing 0.1 g ethyl maltol standards, which was then dissolved in methanol and constant volume in a 100 mL brown volumetric flask, to prepared 1000 mg/L standard solution.
C19 n-alkanes (0.0100 g) were accurately weighed in a 100 mL volumetric flask and dissolved in a fixed volume of dichloromethane to prepare 100.0 mg/L of the internal standard solution.
3.6. Glme Working Principle and Operation Conditions
A 10 µL ethyl maltol standard solution or a 0.100 g sample was precisely weighed into a sample tube filled with quartz glass wool and an appropriate amount of anhydrous sodium sulphate. Then, 10 µL of the internal standard solution was added to the sample tube. Afterwards, the sample tube was moved to the sample pool, and the sample pool was sealed with a rubber stopper. An amount of 50 µL methanol extraction phase was added to a 200 µL inner lining tube as the accepting phase and placed in the condensation tank. GLME conditions were set as: extraction temperature of 270 °C, carrier gas (Nitrogen) speed of 2.5 mL/min, condensation temperature of −2 °C, and extraction time of 7 min. After running the GLME program to the termination of the set time, the acceptor phase volume was eluted and fixed to 100 µL, and the sample was mixed by vortex shaking and finally examined by GC-MS analysis [28].
3.7. Principal Component Analysis
This study aims to use the idea of dimensionality reduction to transform multiple indicators into a few comprehensive indicators (i.e., principal components), where each principal component can reflect most of the information of the original variables, and the contained information does not repeat.
3.8. Quantitative Calculation of Samples
Calibration was performed using C19 as an internal standard to quantify the components containing standards. Assuming that the relative response factor was 1 and the recovery rate was 100%, the provisional determination of components without the standard was quantified relative to the internal standard. The specific formula used to calculate the compounds’ mass (Mi) from the peak area ratio is shown in Equation (2), and the specific formula used to calculate the concentration of substances is shown in Equation (3):
Mi = Ai/As × Fi × Ms
Ci = Mi/m
In Equations (2) and (3), represents the peak area of the designated component, is the peak area of the internal standard, is the mass of the designated component, is the mass of the internal standard, is the relative correction factor, which is assumed to be 1, is the concentration of the designated component, m is the mass of sample.
4. Conclusions
Qualitative and quantitative analyses of volatile flavours and fragrances in ice cream were conducted by a gas-liquid microextraction/GC-MS method. Statistically, it was found that alcohols, acids, esters, ketones, aldehydes, and heterocycles were the principal components in the aromas of ice cream samples. Additionally, Furan-3-carboxaldehyde, 3-furanmethanol, 2(5H)-furanone, 5-methylfurfural, 2,5-diformylfuran, 3-hydroxy-2-methyl-4-pyrone, 5-hydroxymethylfurfural, ethyl maltol, and glycerine were routinely used flavour components. The applicability and safety contents of these components can be obtained in China GB 2760-2014 and in the Flavor and Extract Manufacturers Association (FEMA) of the United States. We summarized the conventional flavours and fragrances used in casual foods, represented by ice cream, to provide an effective reference basis for future research on flavour and fragrance components in foods.
With the improvement of people’s living standards, the variety and taste of food is increasing. Thus, the use of flavours and fragrances will also increase. In future research work, it is possible to combine computer technology, statistics, and other methods to build a library of characteristic fingerprint profiles of flavours and fragrances in the context of a large amount of data, enabling the analysis of flavours and fragrances to reach a state of cloud sharing.
Author Contributions
Conceptualization, L.M. and G.L.; software, Y.L. and L.Y; formal analysis, Q.T. and L.Y; investigation, Q.T., Y.L., X.M. and P.H.; resources, L.M. and G.L; writing—original draft preparation, X.M. and L.Y.; supervision, G.L.; funding acquisition, L.M. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by Jilin Province Science and Technology Department Funding, grant number 20220101074JC and Climbing Project Fund of Changchun University Funding, grant number ZKP202121.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Data will be made available on request.
Conflicts of Interest
We declare that we have no conflicts of interest to this work. we do not have any commercial or associative interest that represents a conflict of interest in connection with the work submitted.
Sample Availability
Not applicable.
References
- Shimoda, M.; Shiratsuchi, H.; Nakada, Y.; Wu, Y.; Osajima, Y. Identification and sensory characterization of volatile flavor compounds in sesame seed oil. J. Agric. Food Chem. 1996, 44, 3909–3912. [Google Scholar] [CrossRef]
- Schrankel, K.R. Safety evaluation of food flavorings. Toxicology 2004, 198, 203–211. [Google Scholar] [CrossRef] [PubMed]
- Wu, X.; He, W.; Yang, Q.; Xu, X.; Jin, Y. Study on extraction process of hyssopus essential oil by hydro-distillation. Food Res. Dev. 2016, 37, 39–41. [Google Scholar]
- Cecati, F.M.; Cid, F.D.; Ardanaz, C.; Kurina-Sanz, M. Eupatorium buniifolium aroma profile assessment by HS-SPME, steam distillation and organic solvent extraction. J. Essent. Oil Res. 2021, 33, 80–93. [Google Scholar] [CrossRef]
- Wu, T.; Mao, L. Influences of hot air drying and microwave drying on nutritional and odorous properties of grass carp (Ctenopharyngodon idellus) fillets. Food Chem. 2008, 110, 647–653. [Google Scholar] [CrossRef]
- Long, B.; Wang, X.; Zhang, F.; Cao, J.; Liu, Y. Analysis of volatile flavor compounds of farmed silurus meridionalischen meat by simultaneous distillation extraction and gas chromatography-mass spectrometry distillation extraction and gas chromatography-mass spectrometry. Food Sci. 2013, 34, 188–192. [Google Scholar]
- Peng, W.U.; Zhou, T.; Kou, L.J.; Wang, C. Automatic Static Headspace GC-MS Analysis of Flavor Compounds in Two Jiaozhou Chinese Cabbage Varieties and Tai an Chinese Cabbage. Food Sci. 2009, 30, 215–218. [Google Scholar]
- Jeleń, H.; Gracka, A.; Myśków, B. Static headspace extraction with compounds trapping for the analysis of volatile lipid oxidation products. Food Anal. Methods 2017, 10, 2729–2734. [Google Scholar] [CrossRef] [Green Version]
- Yatoo, G.N.; Wani, H.; Shah, S.A.; Zargar, M.I.; Rather, M.A.; Banday, J.A. Gas chromatographic-mass spectrometric analysis, antibacterial, antioxidant and antiproliferative activities of the needle essential oil of Abies pindrow growing wild in Kashmir, India. Microb. Pathog. 2021, 158, 105013. [Google Scholar]
- Kamimura, G.; Matsuura, H. Separation of ZnCl2 from less-volatile chlorides by vacuum distillation. Metall. Mater. Trans. B 2020, 51, 1395–1405. [Google Scholar] [CrossRef]
- Rong, L.I.; Jiang, Z.T. Analysis of chemical composition of volatile oil of natural spice, Origanum vulgare L.obtained by supercritical fluid extraction. China Condiment 2011, 36, 107–114. [Google Scholar]
- Conde-Hernández, L.A.; Espinosa-Victoria, J.R.; Guerrero-Beltrán, J.Á. Supercritical extraction of essential oils of Piper auritum and Porophyllum ruderale. J. Supercrit. Fluids 2017, 127, 97–102. [Google Scholar] [CrossRef]
- Cao, Y.P.; Zhang, D. Analysis of Volatile Compounds from Baked and Hot Air-dried Sichuan Pepper (Zanthoxylum piperitum DC.) Using Solid-phase Micro-extraction Coupled with Gas Chromatography-mass Spectrometry. Food Sci. 2011, 32, 190–193. [Google Scholar]
- Zheng, Y.; Xiu-Li, X.U.; Shun-Li, J.I.; Yuan, F.; Huang, Z.Q.; Yang, B.C.; Zhang, F. Determination of Three Restricted Flavor Additives in Cigarettes by Solid-phase Extraction with Gas Chromatography-Tandem Mass Spectrometry. J. Instrum. Anal. 2016, 35, 987–992. [Google Scholar]
- Nandiwale, K.Y.; Galande, N.D.; Bokade, V.V. Process optimization by response surface methodology for transesterification of renewable ethyl acetate to butyl acetate biofuel additive over borated USY zeolite. RSC Adv. 2015, 5, 17109–17116. [Google Scholar] [CrossRef]
- Yang, C.; Piao, X.; Qiu, J.; Wang, X.; Ren, C.; Li, D. Gas purge microsyringe extraction for quantitative direct gas chromatographic-mass spectrometric analysis of volatile and semivolatile chemicals. J. Chromatogr. A 2011, 1218, 1549–1555. [Google Scholar] [CrossRef]
- Nan, J.; Wang, J.; Piao, X.; Yang, C.; Wu, X.; Quinto, M.; Li, D. Novel and rapid method for determination of organophosphorus pesticide residues in edible fungus using direct gas purge microsyringe extraction coupled on-line with gas chromatography–mass spectrometry. Talanta 2015, 142, 64–71. [Google Scholar] [CrossRef]
- Wang, C.; Liu, W.; Wei, Y.; Song, H. Dynamic Changes of the Total Content of Glycoside Aroma Components in Tobacco Leaves in Different Producing Areas During the Late Growth Period. J. Plant Sci. 2018, 6, 164–172. [Google Scholar]
- Legako, J.F.; Cramer, T.; Yardley, K.; Murphy, T.J.; Gardner, T.; Chail, A.; Pitcher, L.R.; MacAdam, J.W. Retail stability of three beef muscles from grass-, legume-, and feedlot-finished cattle. J. Anim. Sci. 2018, 96, 2238–2248. [Google Scholar] [CrossRef] [Green Version]
- Guo, B.B.; Zhang, X.; Meng, L.I.; Zhang, Y.Y.; Sun, B.G.; Chen, H.T.; Tian, H.Y. Analysis of Volatile Flavor Constituents of Wuxi Sauce Sparerib by SPME-GC-MS and SDE-GC-MS. Fine Chem. 2014, 31, 732–733. [Google Scholar]
- Wojdylo, A.; Figureiel, A.; Legua, P.; Lech, K.; Carbonell-Barrachina, A.A.; Hernandez, F. Chemical composition, antioxidant capacity, and sensory quality of dried jujube fruits as affected by cultivar and drying method. Food Chem. 2016, 207, 170–179. [Google Scholar] [CrossRef] [PubMed]
- Fan, W.; Qian, M.C. Headspace solid phase microextraction and gas chromatography− olfactometry dilution analysis of young and aged Chinese “Yanghe Daqu” liquors. J. Agric. Food Chem. 2005, 53, 7931–7938. [Google Scholar] [CrossRef] [PubMed]
- Yan, D.; Zheng, F.P.; Wang, N.; Chen, H.T.; Huang, M.Q.; Sun, B.G. Analysis of Volatiles in Sauced Beef by Microwave-Assisted Extraction Coupled with Solvent-Assisted Flavor Evaporation and Gas Chromatography-Mass Spectrometry. Food Sci. 2013, 34, 250–254. [Google Scholar]
- Mayuoni-Kirshinbaum, L.; Tietel, Z.; Porat, R.; Ulrich, D. Identification of aroma-active compounds in ‘Wonderful’ pomegranate fruit using solvent-assisted flavour evaporation and headspace solid-phase micro-extraction methods. Eur. Food Res. Technol. 2012, 235, 277–283. [Google Scholar] [CrossRef]
- Api, A.; Belsito, D.; Bhatia, S.; Bruze, M.; Calow, P.; Dagli, M.; Dekant, W.; Fryer, A.; Kromidas, L.; La Cava, S. RIFM fragrance ingredient safety assessment, allyl (cyclohexyloxy) acetate, CAS registry number 68901-15-5. Food Chem. Toxicol. 2015, 82, S59–S65. [Google Scholar] [CrossRef]
- Beiranvand, M.; Ghiasvand, A. Simple, Low-Cost and Reliable Device for Vacuum-Assisted Headspace Solid-Phase Microextraction of Volatile and Semivolatile Compounds from Complex Solid Samples. Chromatographia 2017, 80, 1771–1780. [Google Scholar] [CrossRef]
- Xiao, Z.J.; Gen-Rong, L.I.; Duan, Y.P.; Hua, H.U.; Zheng, H.L.; Zhu, Y.H.J.F.C. Analysis of Volatile Components from Essence of Soy Sauces and Caramels. Fine Chem. 2009, 26, 1200–1205. [Google Scholar]
- Yang, C.; Zhao, J.; Wang, J.; Yu, H.; Piao, X.; Li, D. Water-based gas purge microsyringe extraction coupled with liquid chromatography for determination of alkylphenols from sea food Laminaria japonica Aresh. J. Chromatogr. A 2013, 1300, 38–42. [Google Scholar] [CrossRef]
Figure 1.
Effect of four factors to spiked recovery rate: extraction temperatures (a), extraction time (b), carrier gas speed (c), and condensation temperature (d).
Figure 1.
Effect of four factors to spiked recovery rate: extraction temperatures (a), extraction time (b), carrier gas speed (c), and condensation temperature (d).
Figure 2.
Effect of factors AC, BD, and CD interaction response surface.
Figure 3.
Chromatograms of ice cream sample 1 (a) and sample 2 (b).
Figure 4.
Ratio of functional groups of ice cream samples (a) and Volatile aroma loading diagram of ice cream samples (b).
Figure 4.
Ratio of functional groups of ice cream samples (a) and Volatile aroma loading diagram of ice cream samples (b).
Figure 5.
Results of variance analysis of volatile aroma components in ice cream samples.
Figure 6.
Total quality concentrations of the functional groups in ice cream samples.
Figure 7.
Gas-liquid microextraction.
Table 1.
Response to ANOVA for the spiked recovery rate of ethyl maltol samples.
| Scheme | Sum of Squares | df | Mean SQUARE | F-Value | p-Value | |
|---|---|---|---|---|---|---|
| Model | 20.28 | 14 | 1.45 | 97.37 | <0.0001 | significant |
| A-Extraction temperature | 8.82 | 1 | 8.82 | 593.04 | <0.0001 | |
| B-Extraction time | 0.2791 | 1 | 0.2791 | 18.76 | 0.0007 | |
| C-Carrier gas speed | 1.45 | 1 | 1.45 | 97.39 | <0.0001 | |
| D-Condensation temperature | 0.1704 | 1 | 0.1704 | 11.45 | 0.0045 | |
| AB | 0.0121 | 1 | 0.0121 | 0.8132 | 0.3824 | |
| AC | 0.2916 | 1 | 0.2916 | 19.60 | 0.0006 | |
| AD | 0.0042 | 1 | 0.0042 | 0.2840 | 0.6025 | |
| BC | 0.0420 | 1 | 0.0420 | 2.82 | 0.1150 | |
| BD | 0.3600 | 1 | 0.3600 | 24.20 | 0.0002 | |
| CD | 0.6724 | 1 | 0.6724 | 45.19 | <0.0001 | |
| A² | 8.01 | 1 | 8.01 | 538.13 | <0.0001 | |
| B² | 0.2687 | 1 | 0.2687 | 18.06 | 0.0008 | |
| C² | 0.8690 | 1 | 0.8690 | 58.40 | <0.0001 | |
| D² | 0.3097 | 1 | 0.3097 | 20.82 | 0.0004 | |
| Residual | 0.2083 | 14 | 0.0149 | |||
| Lack of Fit | 0.2083 | 10 | 0.0208 | 1.041 × 105 | <0.0001 | significant |
| Pure Error | 8.000 × 10−7 | 4 | 2.000 × 10−7 | |||
| Cor Total | 20.49 | 28 |
Table 2.
Identification results of ice cream samples 1–10 by GC-MS.
| Sample | 1 | Sample | 2 | ||||
|---|---|---|---|---|---|---|---|
| Retention time/min | CAS | Compound | FEMA | Retention time/min | CAS | Compound | FEMA |
| 3.395 | 623-53-0 | Ethyl-methylcarbonate | - | 3.55 | 64-18-6 | Formic Acid | 2487 |
| 3.55 | 64-18-6 | Formic Acid | 2487 | 3.825 | 64-19-7 | Acetic acid | 2006 |
| 3.68 | 56-81-5 | Glycerol | 2525 | 3.995 | 116-09-6 | Acetol | 4462 |
| 3.850 | 64-19-7 | Acetic acid | 2006 | 4.6 | 56-81-5 | Glycerol | 2525 |
| 3.99 | 57-55-6 | Propylene Glycol | 2940 | 4.935 | 57-55-6 | Propylene Glycol | 2940 |
| 4.1 | 116-09-6 | Acetol | 4462 | 5.35 | 625-86-5 | 2,5-Dimethylfuran | 4106 |
| 4.59 | 68-12-2 | N, N-Dimethylformamide | - | 5.75 | 498-60-2 | 3-Furaldehyde | 3737 |
| 4.975 | 107-92-6 | Butyric Acid | 2221 | 6.8 | 4412-91-3 | 3-Furancarbinol | - |
| 5.485 | 98-01-1 | Furfural | 2489 | 7 | 1759-71-3 | cis-1,2-Cyclohexanediol diacetate | - |
| 5.58 | 498-60-2 | Furan-3-carboxaldehyde | 3737 | 7.775 | 1192-62-7 | 1-(Furan-2-yl)ethanone | 3163 |
| 6.085 | 4412-91-3 | 3-Furanmethanol | - | 8.1 | 497-23-4 | 2(5H)-Furanone | 4138 |
| 6.24 | 98-00-0 | Furfuryl alcohol | 2491 | 9.305 | 620-02-0 | 5-Methyl furfural | 2702 |
| 6.86 | 606-45-1 | Methyl 2-methoxybenzoate | 2717 | 10.02 | 924-88-9 | Diisopropyl succinate | - |
| 7.195 | 108-94-1 | Cyclohexanone | 3909 | 11.45 | 80-71-7 | Methyl cyclopentenolone | 2700 |
| 7.64 | 1192-62-7 | 2-Acetylfuran | 3163 | 13.135 | 611-13-2 | Methyl 2-furoate | 2703 |
| 8.4 | 591-11-7 | BETA-ANGELICA LACTONE | 4438 | 14.14 | 118-71-8 | Maltol | 2656 |
| 8.96 | 16867-04-2 | 2,3-Dihydroxypyridine | - | 16.535 | 124-07-2 | Octanoic acid | 2799 |
| 9.175 | 620-02-0 | 5-Methyl furfural | 2702 | 17.6 | 4412-96-8 | 3-Methyl-2-furoic acid | - |
| 9.8 | 925-15-5 | Dipropyl succinate | - | 19.06 | 67-47-0 | 5-Hydroxymethylfurfural | - |
| 11.84 | 110-13-4 | Acetonyl acetone | - | 19.97 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - |
| 12.485 | 3658-77-3 | 4-Hydroxy-2,5-dimethyl-3(2H)furanone | 3174 | 20.625 | 4282-34-2 | 2,5-Thiophenedicarboxylic acid dimethyl ester | - |
| 12.835 | 504-15-4 | Orcinol | 3102 | 21.86 | 334-48-5 | Decanoic acid | 2364 |
| 13.07 | 696-11-7 | 1-methyl-1,3-diazinane-2,4-dione | - | 24.275 | 706-14-9 | γ-Decanolactone | 2360 |
| 15.025 | 28564-83-2 | 4H-pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl- | - | 26.275 | 143-07-7 | Lauric acid | 2614 |
| 16.245 | 1073-96-7 | 3,5-dihydroxy-2-methylpyran-4-one | - | 27.1 | 4437-22-3 | 2,2’-(Oxybis(methylene)) difuran | 3337 |
| 16.49 | 4940-11-8 | Ethyl maltol | 3487 | 27.395 | 77-93-0 | Triethyl citrate | 3083 |
| 17.845 | 67-47-0 | 5-Hydroxymethylfurfural | - | 28.635 | 544-63-8 | Myristic acid | 2764 |
| 19.83 | 10551-58-3 | 5-Acetoxymethyl-2-Furaldehyde | - | ||||
| 23.145 | 2705-87-5 | Allyl cyclohexylpropionate | 2026 | ||||
| Sample | 3 | Sample | 4 | ||||
| Retention time/min | CAS | Compound | FEMA | Retention time/min | CAS | Compound | FEMA |
| 3.57 | 64-18-6 | Formic Acid | 2487 | 3.415 | 64-18-6 | Formic Acid | 2487 |
| 3.855 | 64-19-7 | acetic acid | 2006 | 3.71 | 64-19-7 | acetic acid | 2006 |
| 4.1 | 116-09-6 | acetol | 4462 | 3.92 | 116-09-6 | acetol | 4462 |
| 4.61 | 56-81-5 | glycerol | 2525 | 4.46 | 56-81-5 | glycerol | 2525 |
| 5.13 | 617-35-6 | Ethylpyruvate | 2457 | 5.315 | 98-01-1 | Furfural | 2489 |
| 5.35 | 2041-15-8 | 1,3,5-Cyclohexanetriol | - | 5.77 | 498-60-2 | 3-Furaldehyde | 3737 |
| 5.75 | 498-60-2 | 3-Furaldehyde | 3737 | 6.7 | 4412-91-3 | 3-Furancarbinol | - |
| 6.75 | 4412-91-3 | 3-Furancarbinol | - | 7.75 | 1192-62-7 | 1-(Furan-2-yl)ethanone | 3163 |
| 8.05 | 497-23-4 | 2(5H)-Furanone | 4138 | 8.01 | 497-23-4 | 2(5H)-Furanone | 4138 |
| 8.96 | 16867-04-2 | hydroxypyridone | - | 8.985 | 2361-27-5 | 2-Thiophenecarbohydrazide | - |
| 9.255 | 620-02-0 | 5-Methyl furfural | 2702 | 9.285 | 620-02-0 | 5-Methyl furfural | 2702 |
| 10.025 | 924-88-9 | Diisopropyl succinate | - | 10 | 925-15-5 | Dipropyl succinate | - |
| 10.46 | 765-70-8 | Maple lactone | - | 10.475 | 637-88-7 | 1,4-Cyclohexanedione | - |
| 11.235 | 5989-27-5 | (+)-Limonene | 2633 | 11.445 | 80-71-7 | Methyl cyclopentenolone | 2700 |
| 11.405 | 80-71-7 | Methyl cyclopentenolone | 2700 | 11.975 | 110-13-4 | Acetonylacetone | - |
| 11.985 | 3128-07-2 | 6-Oxoheptanoic acid | - | 12.96 | 823-82-5 | 2,5-Furandicarbaldehyde | - |
| 12.46 | 1192-62-7 | 1-(Furan-2-yl)ethanone | 3163 | 13.115 | 611-13-2 | Methyl 2-furoate | 2703 |
| 12.975 | 3658-77-3 | 4-Hydroxy-2,5-dimethylfuran-3(2H)-one | 3174 | 14.11 | 118-71-8 | Maltol | 2656 |
| 13.1 | 611-13-2 | Methyl 2-furoate | 2703 | 16.19 | 1193-79-9 | 1-(5-Methylfuran-2-yl)ethanone | 3609 |
| 13.635 | 590-86-3 | Isovaleraldehyde | 2692 | 19.225 | 67-47-0 | 5-hydroxymethylfurfural | - |
| 13.92 | 98-00-0 | Furfuryl alcohol | 2491 | 20 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - |
| 14.055 | 118-71-8 | Maltol | 2656 | 20.99 | 102-76-1 | Triacetin | 2007 |
| 17.4 | 18720-62-2 | 2-methylheptan-3-ol | - | 25.855 | 498-07-7 | Levoglucosan | - |
| 17.56 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - | 28.605 | 544-63-8 | Myristic acid | 2764 |
| 18.85 | 67-47-0 | 5-hydroxymethylfurfural | - | 29.52 | 84-69-5 | Diisobutyl phthalate | - |
| 21.76 | 112-37-8 | Undecanoic acid | 3245 | ||||
| 23.16 | 2705-87-5 | Allyl 3-cyclohexylpropionate | 2026 | ||||
| 27.09 | 3777-69-3 | 2-Amylfuran | 3317 | ||||
| 28.605 | 544-63-8 | Myristic acid | 2764 | ||||
| Sample | 5 | Sample | 6 | ||||
| Retention time/min | CAS | Compound | FEMA | Retention time/min | CAS | Compound | FEMA |
| 3.155 | 64-18-6 | Formic Acid | 2487 | 3.055 | 64-18-6 | Formic Acid | 2487 |
| 3.43 | 64-19-7 | acetic acid | 2006 | 3.33 | 116-09-6 | acetol | 4462 |
| 3.635 | 116-09-6 | acetol | 4462 | 3.615 | 627-03-2 | Ethoxyacetic acid | - |
| 3.94 | 79-09-4 | Propionic acid | - | 3.94 | 56-81-5 | glycerol | 2525 |
| 4.19 | 3393-64-4 | 4-hydroxy-3-methylbutan-2-one | - | 4.22 | 3121-61-7 | 2-Methoxyethyl acrylate | - |
| 4.245 | 56-81-5 | glycerol | 2525 | 4.475 | 1117-97-1 | N-methoxymethanamine | - |
| 5.31 | 98-01-1 | Furfural | 2489 | 5.385 | 498-60-2 | 3-Furaldehyde | 3737 |
| 5.71 | 498-60-2 | 3-Furaldehyde | 3737 | 5.65 | 98-01-1 | Furfural | 2489 |
| 6.555 | 4412-91-3 | 3-Furancarbinol | - | 6.375 | 4412-91-3 | 3-Furancarbinol | - |
| 7.73 | 1192-62-7 | 1-(Furan-2-yl)ethanone | 3163 | 6.93 | 930-60-9 | 2-Cyclopentene-1,4-dione | - |
| 7.89 | 497-23-4 | 2(5H)-Furanone | 4138 | 7.73 | 497-23-4 | 2(5H)-Furanone | 4138 |
| 8.995 | 16867-04-2 | hydroxypyridone | - | 8.85 | 5380-42-7 | 2-(Carbomethoxy)thiophene | - |
| 9.27 | 620-02-0 | 5-Methyl furfural | 2702 | 8.975 | 16867-04-2 | hydroxypyridone | - |
| 9.81 | 53119-25-8 | 1-thiophen-2-ylpentan-1-one | - | 9.235 | 620-02-0 | 5-Methyl furfural | 2702 |
| 9.95 | 925-15-5 | Dipropyl succinate | - | 9.6 | 675-10-5 | triacetate lactone | - |
| 11.35 | 80-71-7 | Methyl cyclopentenolone | 2700 | 9.75 | 88-15-3 | 2-Acetylthiophene | - |
| 11.945 | 1117-31-3 | 1,3-butanediol diacetate | - | 11.275 | 80-71-7 | Methyl cyclopentenolone | 2656 |
| 12.965 | 504-15-4 | Orcinol | - | 11.885 | 110-13-4 | Acetonylacetone | - |
| 13.07 | 611-13-2 | Methyl 2-furoate | 2703 | 12.035 | 19432-69-0 | Methyl 5-methylthiophene-2-carboxylate | - |
| 13.9 | 98-00-0 | Furfuryl alcohol | 2491 | 12.755 | 3658-77-3 | 4-Hydroxy-2,5-dimethylfuran-3(2H)-one | 3174 |
| 14.11 | 118-71-8 | Maltol | 2656 | 12.855 | 823-82-5 | 2,5-Furandicarbaldehyde | - |
| 14.65 | 7492-38-8 | 2-methyloctan-4-one | - | 12.985 | 611-13-2 | Methyl 2-furoate | 2703 |
| 15.32 | 1540-29-0 | Ethyl 2-acetylhexanoate | 4452 | 13.44 | 110-62-3 | Valeraldehyde | 3098 |
| 18.9 | 67-47-0 | 5-hydroxymethylfurfural | - | 13.935 | 118-71-8 | Maltol | 2656 |
| 19.36 | 6434-78-2 | trans-2-nonene | - | 14.625 | 629-62-9 | pentadecane | - |
| 19.96 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - | 16.395 | 501-30-4 | kojic acid | - |
| 20.635 | 4282-34-2 | 2,5-Thiophenedicarboxylic acid dimethyl este | - | 17.505 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - |
| 26.215 | 498-07-7 | Levoglucosan | - | 18.38 | 67-47-0 | 5-hydroxymethylfurfural | - |
| 27.63 | 6968-62-3 | D-ERYTHRO-l-TALO-OCTONIC ACID, γ-LACTONE | - | 20.6 | 4282-34-2 | 2,5-Thiophenedicarboxylic acid dimethyl este | - |
| 29.525 | 84-69-5 | Diisobutyl phthalate | - | 20.905 | 102-76-1 | Triacetin | 2007 |
| 25.5 | 498-07-7 | Levoglucosan | - | ||||
| 25.89 | 2311-46-8 | propan-2-yl hexanoate | 2950 | ||||
| 26.15 | 143-07-7 | Lauric acid | 2614 | ||||
| 28.595 | 544-63-8 | Myristic acid | 2764 | ||||
| 29.52 | 84-69-5 | Diisobutyl phthalate | - | ||||
| Sample | 7 | Sample | 8 | ||||
| Retention time/min | CAS | Compound | FEMA | Retention time/min | CAS | Compound | FEMA |
| 3.25 | 64-18-6 | Formic Acid | 2487 | 3.305 | 64-18-6 | Formic Acid | 2487 |
| 3.38 | 141-46-8 | Glycolaldehyde | - | 3.52 | 64-19-7 | acetic acid | 2006 |
| 3.46 | 64-19-7 | acetic acid | 2006 | 3.81 | 116-09-6 | acetol | 4462 |
| 3.68 | 116-09-6 | acetol | 4462 | 4.04 | 623-53-0 | Ethyl-methylcarbonat | - |
| 3.945 | 623-53-0 | Ethyl-methylcarbonat | - | 4.305 | 56-81-5 | glycerol | 2525 |
| 4.235 | 56-81-5 | glycerol | 2525 | 4.6 | 4254-15-3 | (S)-(+)-1,2-Propanediol | - |
| 4.565 | 4254-15-3 | (S)-(+)-1,2-Propanediol | - | 5.3 | 98-01-1 | Furfural | 2489 |
| 5.3 | 98-01-1 | Furfural | 2489 | 5.71 | 498-60-2 | 3-Furaldehyde | 3737 |
| 5.675 | 498-60-2 | 3-Furaldehyde | 3737 | 6.6 | 4412-91-3 | 3-Furancarbinol | - |
| 6.575 | 4412-91-3 | 3-Furancarbinol | - | 7.915 | 497-23-4 | 2(5H)-Furanone | 4138 |
| 7.885 | 497-23-4 | 2(5H)-Furanone | 4138 | 8.995 | 16867-04-2 | hydroxypyridone | - |
| 8.85 | 22913-26-4 | Methyl thiophene-3-carboxylate | - | 9.26 | 620-02-0 | 5-Methyl furfural | 2702 |
| 8.985 | 16867-04-2 | hydroxypyridone | - | 9.965 | 924-88-9 | Diisopropyl succinate | - |
| 9.235 | 620-02-0 | 5-Methyl furfural | 2702 | 11.325 | 80-71-7 | Methyl cyclopentenolone | 2700 |
| 9.96 | 924-88-9 | Diisopropyl succinate | - | 12.94 | 823-82-5 | 2,5-Furandicarbaldehyde | - |
| 12.935 | 504-15-4 | Orcinol | - | 13.03 | 611-13-2 | Methyl 2-furoate | 2703 |
| 13.045 | 611-13-2 | Methyl 2-furoate | 2703 | 13.93 | 118-71-8 | Maltol | 2656 |
| 17.52 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - | 17.515 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - |
| 18.74 | 67-47-0 | 5-hydroxymethylfurfural | - | 18.695 | 67-47-0 | 5-hydroxymethylfurfural | - |
| 19.93 | 118-71-8 | Maltol | 2656 | 20.605 | 4282-34-2 | 2,5-Thiophenedicarboxylic acid dimethyl este | - |
| 20.945 | 102-76-1 | Triacetin | 2007 | 25.52 | 498-07-7 | Levoglucosan | - |
| 25.52 | 498-07-7 | Levoglucosan | - | 29.52 | 84-69-5 | Diisobutyl phthalate | - |
| 29.525 | 84-69-5 | Diisobutyl phthalate | - | ||||
| Sample | 9 | Sample | 10 | ||||
| Retention time/min | CAS | Compound | FEMA | Retention time/min | CAS | Compound | FEMA |
| 3.54 | 64-18-6 | Formic Acid | 2487 | 4.01 | 64-18-6 | Formic Acid | 2487 |
| 3.795 | 64-19-7 | acetic acid | 2006 | 4.205 | 64-19-7 | acetic acid | 2006 |
| 4.06 | 116-09-6 | acetol | 4462 | 4.46 | 116-09-6 | acetol | 4462 |
| 4.3 | 79-09-4 | Propionic acid | 2924 | 4.635 | 56-81-5 | glycerol | 2525 |
| 4.635 | 56-81-5 | glycerol | 2525 | 5.18 | 4254-15-3 | (S)-(+)-1,2-Propanediol | - |
| 4.935 | 4254-15-3 | (S)-(+)-1,2-Propanediol | - | 5.795 | 498-60-2 | 3-Furaldehyde | 3737 |
| 5.79 | 498-60-2 | 3-Furaldehyde | 3737 | 6.92 | 4412-91-3 | 3-Furancarbinol | - |
| 6.74 | 4412-91-3 | 3-Furancarbinol | - | 8.095 | 497-23-4 | 2(5H)-Furanone | 4138 |
| 7.78 | 1192-62-7 | 2-Acetylfuran | 3163 | 8.765 | 591-12-8 | a-Angelic lactone | 3293 |
| 8.04 | 497-23-4 | 2(5H)-Furanone | 4138 | 8.895 | 16867-04-2 | hydroxypyridone | - |
| 9.015 | 16867-04-2 | hydroxypyridone | - | 8.99 | 22913-26-4 | Methyl thiophene-3-carboxylate | - |
| 9.28 | 620-02-0 | 5-Methyl furfural | 2702 | 9.28 | 620-02-0 | 5-Methyl furfural | 2702 |
| 10.04 | 924-88-9 | Diisopropyl succinate | - | 10.025 | 925-15-5 | Dipropyl succinate | - |
| 11.4 | 80-71-7 | Methyl cyclopentenolone | 2700 | 11.95 | 110-13-4 | Acetonylacetone | - |
| 12.96 | 504-15-4 | Orcinol | - | 12.765 | 3658-77-3 | 4-Hydroxy-2,5-dimethylfuran-3(2H)-one | 3174 |
| 13.09 | 611-13-2 | Methyl 2-furoate | 2703 | 12.945 | 504-15-4 | Orcinol | - |
| 16.63 | 4940-11-8 | Ethyl maltol | 3487 | 13.07 | 611-13-2 | Methyl 2-furoate | 2703 |
| 17.55 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - | 13.885 | 98-00-0 | Furfuryl alcohol | 2491 |
| 19.1 | 67-47-0 | 5-hydroxymethylfurfural | - | 17.54 | 10551-58-3 | (5-Formyl-2-furyl)methyl acetate | - |
| 19.95 | 118-71-8 | Maltol | 2656 | 19.14 | 67-47-0 | 5-hydroxymethylfurfural | - |
| 25.57 | 498-07-7 | Levoglucosan | - | 25.715 | 498-07-7 | Levoglucosan | - |
| 29.52 | 84-69-5 | Diisobutyl phthalate | - | ||||
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Mu, L.; Tong, Q.; Liu, Y.; Meng, X.; He, P.; Li, G.; Ye, L. Application of Gas-Liquid Microextraction (GLME)/GC-MS for Flavour and Fragrance in Ice Cream Detection and Composition Analysis. Molecules 2023, 28, 522. https://doi.org/10.3390/molecules28020522
AMA Style
Mu L, Tong Q, Liu Y, Meng X, He P, Li G, Ye L. Application of Gas-Liquid Microextraction (GLME)/GC-MS for Flavour and Fragrance in Ice Cream Detection and Composition Analysis. Molecules. 2023; 28(2):522. https://doi.org/10.3390/molecules28020522
Chicago/Turabian StyleMu, Li, Qi Tong, Yuhang Liu, Xianglong Meng, Peng He, Gang Li, and Linyang Ye. 2023. "Application of Gas-Liquid Microextraction (GLME)/GC-MS for Flavour and Fragrance in Ice Cream Detection and Composition Analysis" Molecules 28, no. 2: 522. https://doi.org/10.3390/molecules28020522
APA StyleMu, L., Tong, Q., Liu, Y., Meng, X., He, P., Li, G., & Ye, L. (2023). Application of Gas-Liquid Microextraction (GLME)/GC-MS for Flavour and Fragrance in Ice Cream Detection and Composition Analysis. Molecules, 28(2), 522. https://doi.org/10.3390/molecules28020522
