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The quality of green coffee is influenced by the degree of ripeness of the fruit at harvest. The aim of this study was to identify chemical markers differentiating between degrees of ripeness. Two coffee varieties, Catuai and Tipica, from the same farm were analysed using the following parameters and methods: caffeine and chlorogenic acid content using high-performance liquid chromatography (HPLC), sucrose content using hydrophilic interaction chromatography, high-molecular weight fraction (HMW) using high-performance size-exclusion chromatography (HPSEC) and volatile compounds using headspace solid phase micro extraction gas chromatography/mass spectrometry. The best method for differentiating between degrees of ripeness was found to be principal component analysis (PCA) based on HPLC data. HPSEC showed differences in the HMW fraction for different degrees of ripeness and both coffee varieties. Volatile profiles allowed separation of both varieties; yet, except for ripe Catuai, no separation was achieved for the degree of ripeness.

This chapter describes the measurement of free radical processes in liquid coffee samples, and their impact on the quality and stability of the beverage. Free radicals generated during the roasting process are relatively stable and located in the polymeric melanoidins, but their concentrations change in coffee solutions via O2-independent decay and O2-dependent formation processes. In addition, the chemistry of coffee solutions is strongly influenced by highly unstable free radicals, presumably hydroxyl radicals generated via Fenton reaction chemistry. These radicals react virtually indiscriminately with organic molecules by hydrogen atom extraction, and can thus initiate progressive degradation of coffee brews. Identification of stable markers of such reactions are discussed along with possible strategies for slowing the rate of alteration of liquid coffee products during storage.

This chapter briefly reviews the roles played by free radical processes during the roasting and storage of coffee beans and solid coffee products. During roasting, free radical production occurs in distinct phases, possibly related to the Maillard and caramelization reactions. At the same time there is also generation of large quantities of molecules with antioxidant properties, thus demonstrating that antioxidant production does not necessarily equate to free radical scavenging, insofar as it is measured by current assays. Furthermore, with respect to chemical components that are associated with desirable sensory properties of coffee, free radical processes may have both beneficial and detrimental effects.

With the growing demand for high-quality coffee, it is becoming increasingly important to establish quantitative measures of the freshness of coffee, or the loss thereof, over time. Indeed, freshness has become a critical quality criterion in the specialty coffee scene, where the aim is to deliver the most pleasant flavor in the cup, from highest quality beans. A series of intensity ratios of selected volatile organic compounds (VOC) in the headspace of coffee (by gas chromatography–mass spectrometry) were revisited, with the aim to establish robust indicators of freshness of coffee – called freshness indices. Roasted whole beans in four different packaging materials and four commercial capsule systems from the Swiss market were investigated over a period of up to one year of storage time. These measurements revealed three types of insight. First, a clear link between barrier properties of the packaging material and the evolution of selected freshness indices was observed. Packaging materials that contain an aluminum layer offer better protection. Second, processing steps prior to packaging are reflected in the absolute values of freshness indices. Third, differences in the standard deviations of freshness-indices for single serve coffee capsule systems are indicative of differences in the consistency among systems, consistency being an important quality attribute of capsules.

Using proton-transfer-reaction time-of-flight mass-spectrometry (PTR-ToF-MS), we investigated the extraction dynamic of 95 ion traces in real time (time resolution: 1 second) during espresso coffee preparation. Fifty-two of these ions were tentatively identified. This was achieved by on-line sampling of the volatile organic compounds (VOCs) in close vicinity to the coffee flow, at the exit of the extraction hose of the espresso machine (single serve capsules). Ten replicates of six different single serve coffee types were extracted to a final volume of between 30 - 110 mL, according to the recommended cup size of the respective coffee capsule (Ristretto, Espresso and Lungo), and analyzed. The results revealed considerable differences in the extraction kinetics between compounds, which led to a fast evolution of the volatile profiles in the extract flow and consequently to an evolution of the final aroma balance in the cup. Besides exploring the time-resolved extraction dynamics of VOCs, the dynamic data also allowed the coffees types (capsules) to be distinguished from one another. Both Hierarchical Cluster Analysis (HCA) and Principal Component Analysis (PCA) showed full separation between the coffees types. The methodology developed provides a fast and simple means of studying the extraction dynamics of VOCs and differentiating between different coffee types.

A platform composed of three complementary and validated antioxidant assays is proposed for the routine and fast assessment of the antioxidant capacity of coffee brews. Firstly, a brief review of the principles underlying antioxidant measurements in foods, and the rationale behind the development of an analytical platform for measuring the antioxidant capacity of coffee is given. A range of complementary methods is described based on either hydrogen atom or electron transfer reactions. Secondly, three total antioxidant capacity (TAC) assays are recommended for the platform. Two are based on electron-transfer reactions—the Folin–Ciocalteu (FC) assay for total phenols, and the ABTS assay, which on oxidation forms the cationic chromophore, 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulphonate) (ABTS•+). The third, which is based on hydrogen-atom transfer, is the oxygen radical absorbance capacity (ORAC), in which the antioxidant and the substrate fluorescein compete for thermally generated peroxyl radicals after their formation by decomposition of 2,​2′-​azobis-​2-​amidinopropane,​dihydrochloride (AAPH). Finally, validated protocols for conducting these three assays, using flow injection analysis (FIA), are presented along with actual results to illustrate their reproducibility and robustness. The three assays are combined into an analytical platform to profile and compare the antioxidant potential of a series of roasted coffee samples. Antioxidant values obtained with the same dark-roast coffee are 2103, 710, and 5868 gallic acid equivalents (GAE) for the FC, ABTS, and ORAC assays, respectively. These numbers thus reflect the different types of chemical reaction that are performed, and illustrate the fact that assays for TAC are actually selective (and hence complementary) for specific types of antioxidant molecule.

Coffee is a major source of dietary antioxidants; some are present in the green bean, whereas others are generated during roasting. However, there is no single accepted analytical method for their routine determination. This paper describes the adaption of three complementary assays (Folin-Ciocalteu (FC), ABTS and ORAC) for the routine assessment of antioxidant capacity of beverages, their validation, and use for determining the antioxidant capacities of extracts from coffee beans at different stages in the roasting process. All assays showed a progressive increase in antioxidant capacity during roasting to a light roast state, consistent with the production of melanoidins having a higher antioxidant effect than the degradation of CGAs. However, the three assays gave different numbers for the total antioxidant capacity of green beans relative to gallic acid (GA), although the range of values was much smaller when chlorogenic acid (CGA) was used as reference. Therefore, although all three assays indicated that there was an increase in antioxidant activity during coffee roasting, and the large differences in responses to GA and CGA illustrate their different sensitivities to different types of antioxidant molecule.

During coffee roasting major changes occur in coffee bean composition. Among others dark coloured melanoidins are formed, which are high molecular weight Maillard reaction products. A new approach is presented here to monitor the influence of roasting conditions on the antioxidant capacity of melanoidins and chlorogenic acids (CGAs) in a coffee brew. Validated Folin–Ciocalteu (FC) and ABTS assays were used as on-line antioxidant assays coupled (post-column) with high performance size-exclusion chromatography (HPSEC). HPSEC enabled the separation of melanoidins from CGAs and the determination of the antioxidant capacity of each fraction, within a total elution time of 25 min. Besides the on-line assay measurements, both assays were also applied off-line with flow injection analysis (FIA). The maximum antioxidant capacity was determined to be at a light-to-medium roast degree, measured with both ABTS-FIA and FC-FIA assays as well as on-line ABTS assay. With FC on-line assay the maximum was found to be at a very light roast degree. Based on the peak areas obtained with the new coupled technique the roasting effects on the variability of melanoidin and CGA contents in coffee brews were studied. The majority of melanoidins are already formed in the early stage of the roasting process and the relative contribution of melanoidins to the total antioxidant capacity increases towards darker roasts, mainly because CGAs degrade during roasting. A new parameter, the ratio of melanoidin to CGA peak area, was introduced as a possible predictor of the roast degree.

Development of liquid coffee products of good quality with extended shelf lives is hampered by their rapid quality degradation as a result of both physical and flavor instability. One approach that is being considered for extending the shelf lives of liquid coffees is that of supplementing the beverage with a very mild and slow continuous extraction from intact roasted beans that are held within an aluminum can. This paper reports the use of electron paramagnetic resonance (EPR) spectroscopy to examine the effects of key parameters that affect the stability of liquid coffee prepared from aqueous extracts from whole roasted coffee beans, namely, the O2 content of the water and headspace during extraction and the temperature during storage. It was found that the magnitude of the free radical signal was sensitive to the O2 content of the water used for extraction and storage time and temperature, whereas the intensity of the Fe(III) (g = 4.3) signal was affected only by the O2 content of the water and the Mn signal was insensitive to the experimental parameters. The most critical factor was the O2 content of the water used for extraction, and careful control of O2 exposure at the extraction stage could be a crucial factor for generating products with resistance to oxidative processes during storage.

Mixed metal clusters of sodium and cesium with gold have been generated in a supersonic expansion from the mixed vapor phase. Their tendency towards binary cluster formation, relative thermodynamic stability, and ionization potentials have been experimentally and computationally investigated. The properties of the NaxAu clusters may be understood within an electronic shell model based on delocalized cluster orbitals, whereas the characteristics of CsxAu are indicative of substantial ionic interactions. Relativistic density functional calculations have been performed to elucidate the cluster electronic structure and to rationalize observed properties which may not be accounted for by the jellium model. The properties of these finite-size clusters are shown to be related to the known bulk intermetallic compounds sodium gold and cesium-gold (cesium aurid), respectively.

� 2016 IOP Publishing Ltd. The persistence of aroma compounds in breath after swallowing is an important attribute of the overall aroma experience during eating and drinking. It is mainly related to the coating of the oral tract with food residues and the interaction between volatile compounds and airway mucosa. We have studied the persistence of eight compounds (2,5-dimethylpyrazine, guaiacol, 4-methylguaiacol, phenylethylalcohol, ethylbutanoate, ethyloctanoate, isoamylacetate and 2-heptanone) both in-nose and in-mouth after administration of volatiles in gas phase (vapor) to five different panelists. By using volatiles in the gas phase, only the interaction with the mucosa is highlighted and the formation of a liquid coating in the oral and tracheal airway is avoided. The physicochemical properties of the compounds, mainly polarity and vapor pressure, determine the interactions of the volatiles with the airway mucosa. The use of different breathing protocols allowed the study of the differences between nasal and oral mucosa in volatile retention, with higher persistence of volatiles obtained in-mouth. Initial concentration also affected persistence, but only for compounds with high volatility and at low concentration.

The influence of roasting and storage conditions on free radical contents of individual Arabica coffee beans was examined during storage of whole, half and ground beans in air over a 1-month period. Free radical contents increased with increasing roasting time (roasting degree), but the atmosphere (air vs. N 2 ) used in the roasting and cooling process had little effect. There was a progressive increase in free radical contents with storage time, but the rate was much lower in whole beans than with half and fully ground beans, for which the rate was similar. These results suggest that exposure to O 2 , rather than physical grinding is the main mechanism for storage-related free radical generation, and strongly indicate that roasted coffee is best kept as whole beans in order to minimise changes during prolonged periods of aerobic storage. Furthermore, they demonstrate that EPR measurements can contribute to understanding the process and storage related changes in coffee.

The preferred fragmentation patterns of negatively charged carbon clusters, C−N have been investigated by cluster—beam impact methods using various surfaces and impact energies (Ei = 0-150 eV). Transitions from one type of cluster structure to another are inferred from the observed change in fragmentation patterns. The results are made possible by the high intact-scattering yield of C−N clusters, and by the competitiveness of fragmentation with electron emission for clusters N < 40. The main inferred structures and diagnostic fragmentation patterns are (i) chain structures (4 < N < 18), which fragment by C(0)3 loss; (ii) ring structures, N ≈ 17-32, reflected by preferential cleavage to give large neutral clusters C(0)14, and C(0)22, (iii) polycyclic or cage structures, which shatter to yield an array of small fragments; and (iv) fullerene-type structures, N > 33, for which electron emission dominates over fragmentation. These results are compared and contrasted with results obtained from other fragmentation and collisional methods.

Die Strukturbildung an Grenzflachen, deren Induktion und Charakterisierung, dadurch bewirkte Fortschritte in der heterogenen Katalyse und die Aufklarung der Struktur elektrochemischer Phasengrenzen sind Schwerpunkte dieses Trendberichts. Von hoher Aktualitat sind auch die zeitaufgeloste Untersuchung chemischer Reaktionen, die Nutzung der Dichtefunktionaltheorie fur neue quantenchemischen Methoden und die Cluster.

Among the 100 different known Coffea species, Coffea arabica L. (Arabica) and Coffea canephora Pierre (Robusta) are the only two of commercial interest. They differ in a range of agronomic, genetic, and chemical properties. Due to the significant price difference between Arabica and Robusta, there is an economic incentive to illicitly replace Arabica with Robusta. Therefore, it is crucial to have accurate methods to determine the Robusta-to-Arabica-ratio in blends. This paper presents the proof of principle of a new and fast approach to determine the Robusta fraction in a blend based on Raman spectroscopy. The oils of two references (a pure Robusta and pure Arabica coffee) and six blends thereof consisting of different Robusta and Arabica fractions were extracted using a Soxhlet system. The solutes were analyzed by means of Raman spectroscopy without further workup. Using the intensity ratio between two Raman peaks, one characteristic for kahweol and one characteristic for fatty acids, allowed determinination of the Robusta content in a given mixture. The intensity ratio is linearly dependent on the Robusta content of the compound. Above a Robusta content of 75 wt %, kahweol was not detectable. The Raman data are in agreement with results obtained from the very time-consuming multistep DIN 10777 procedures based on HPLC.

Because of the roles of free radicals in the formation of Maillard reaction products and as markers of oxidation processes in foods, the dynamics of free radical generation during the roasting of coffee beans have been measured, and some exploratory investigations conducted on the extent to which these are influenced by the bean type, and the atmosphere (air vs. N2), in which the beans were roasted and cooled. The intensities of the free radical signals from individual Arabica and Robusta coffee beans were measured continuously in an EPR spectrometer, whilst beans underwent heating/cooling cycles in air or N2 atmospheres. Additional EPR measurements were performed on the products of coffee beans roasted in a laboratory, convectional hot air roaster. Two sets of experiments were performed: (i) single/half bean roasting in air or N2, and real time, in situ EPR analysis of the free radical content – with a very high flow of roasting gas (convective roasting); (ii) batch roasting in air or N2, and EPR measurements of individual roasted beans – in a rather low flow of gas. Large differences in intermediate and final free radical EPR signal intensities were observed between the specimens of Arabica and Robusta beans that were investigated, irrespective of the roasting atmosphere. During the heating phase of the roasting process, only minor differences were observed between beans of the same type roasted in air or nitrogen, but the presence of oxygen in the cooling cycle resulted in major increases of free radical levels compared to those observed in an inert atmosphere, although this O2-related effect was not observed in beans from the convectional hot air roaster. Large bean to bean variations were observed with a standard blend roasted in the convectional hot air roaster, but much smaller variations were observed with beans from a single batch. Three major conclusions can be drawn from this study: (i) when roasting with a very strong flow of hot gas, the atmosphere (air vs. N2) had a very limited impact (during the heating phase) on free radical formation, but a dramatic and fast increase during the cooling phase, irrespective of the type of coffee beans. (ii) It appears that the relative masses of coffee beans and air during the roasting process are critical for oxidation and hence the free radical content of the final product. Indeed, the dramatic increase in free radicals during air-cooling was only observed if roasting was performed with a very high flow of hot air. (iii) There are wide variations in the free radical dynamics of different types of coffee bean. Arabica beans showed stronger free radical formation during roasting and higher EPR intensities at the end of the roasting cycle, than did Robusta beans. Yet, as the sampling over different Arabicas and Robustas was limited here, a more systematic study is needed to ascertain this observation.

An experimental technique is investigated to separate/enrich fullerenes of metallofullerenes, exploiting differences in sublimation temperatures without the use of solvents. Fullerenes are sublimed out of the soot and deposited on a quartz rod along a temperature gradient (gradient sublimation). In a position-sensitive experiment the composition of the deposit on the rod is monitored by laser-desorption mass spectrometry. Strongly enriched regions containing specific fullerene molecules (i.e., C[sub 84] or LaC[sub 82]) are observed. Furthermore, C[sub 74], which could not be extracted from the soot by organic solvents, sublimes out of the soot. 26 refs., 6 figs.

The authors report the formation of fullerenes from graphite by sputtering and electron beam evaporation. Under conditions that differ dramatically from those in the previously known fullerene production processes, the new methods preferentially yield the soluble higher fullerenes C{sub 70}, C{sub 76}, C{sub 78}, and C{sub 84} in addition to minor amounts of C{sub 60} only. Upon passage of carbon particles formed by electron beam evaporation through an electrostatic field, fullerenes are mainly isolated from the cathode, not from the anode, which supports the formation of cationic intermediates in fullerene growth mechanisms. The variables thought to be important for fullerene production can be controlled efficiently in the new processes. 18 refs., 3 figs.

Surface collisions of negatively charged atomic clusters C N - and Si N - , N

The authors report the formation of fullerenes from graphite by sputtering and electron beam evaporation. Under conditions that differ dramatically from those in the previously known fullerene production processes, the new methods preferentially yield the soluble higher fullerenes C{sub 70}, C{sub 76}, C{sub 78}, and C{sub 84} in addition to minor amounts of C{sub 60} only. Upon passage of carbon particles formed by electron beam evaporation through an electrostatic field, fullerenes are mainly isolated from the cathode, not from the anode, which supports the formation of cationic intermediates in fullerene growth mechanisms. The variables thought to be important for fullerene production can be controlled efficiently in the new processes. 18 refs., 3 figs.

The yield of C60+ ions reflected from the surface of graphite is found to be a bimodal function of the energy of impact. Below 140 eV (6 km/s), the yield decreases with energy and the scattering time-of-flight peak is sharp. Above 170 eV, the yield increases, but the peak is broad and asymmetric, corresponding to delayed electron emission from an impact-heated, neutralized cluster. There is also evidence for fragmentation to C58 and C56. The emission process may be analogous to that reported for scattered C60-. Application of statistical rate theory to either observation (C60± ) gives an estimated 25-30 percent transfer of impact energy into cluster internal modes. The decreasing yield at highest energies (>400 eV) may result from adhesion processes (C60-surface bonding) that could also account for the absence of delayed electron emission in C60-silicon collisions.

A robust and reproducible model was developed to predict the sensory profile of espresso coffee from instrumental headspace data. The model is derived from 11 different espresso coffees and validated using 8 additional espressos. The input of the model consists of (i) sensory profiles from a trained panel and (ii) on-line proton-transfer reaction mass spectrometry (PTR-MS) data. The experimental PTR-MS conditions were designed to simulate those for the sensory evaluation. Sixteen characteristic ion traces in the headspace were quantified by PTR-MS, requiring only 2 min of headspace measurement per espresso. The correlation is based on a knowledge-based standardization and normalization of both datasets that selectively extracts differences in the quality of samples, while reducing the impact of variations on the overall intensity of coffees. This work represents a significant progress in terms of correlation of sensory with instrumental results exemplified on coffee.

Interest in on-line measurements of volatile organic compounds (VOCs) is increasing, as sensitive, compact, and affordable direct inlet mass spectrometers are becoming available. Proton-transfer reaction mass spectrometry (PTR-MS) distinguishes itself by its high sensitivity (low ppt range), high time resolution (200 ms), little ionization-induced fragmentation, and ionization efficiency independent of the compound to be analyzed. Yet, PTR-MS has a shortcoming. It is a one-dimensional technique that characterizes compounds only via their mass, which is not sufficient for positive identification. Here, we introduce a technical and analytical extension of PTR-MS, which removes this shortcoming, while preserving its salient and unique features. Combining separation of VOCs by gas chromatography (GC) with simultaneous and parallel detection of the GC effluent by PTR-MS and electron impact MS, an unambiguous interpretation of complex PTR-MS spectra becomes feasible. This novel development is discussed on the basis of characteristic performance parameters, such as resolution, linear range, and detection limit. The recently developed drift tube with a reduced reaction volume is crucial to exploit the full potential of the setup. We illustrate the performance of the novel setup by analyzing a complex food system.

Personal dietary choices are largely based on flavor preferences. Thus understanding individual flavor perception and preference is vital to understanding the basis of human diet selection. We have developed novel tools to measure in real time and at an individual level volatile aroma compounds delivered breath-by-breath to the nose while eating and drinking. The same food may deliver different aromas to different people, due the specificities of their in-mouth environment (inter-individual differences). Moreover, a person may eat a given food in a different manner, leading to variations in the aroma profile reaching the nose (intra-individual differences). Understanding the basis of these differences opens the door to an individualized aroma science and the road to delivering nutritional value and health through products consumers prefer. The challenge to the food industry is to align what the consumer wants with what the consumer needs, delivering nutritional value and health through products they prefer.

The objective of the project is to develop on-line, real-time, and noninvasive process control tools of coffee roasting that help deliver a consistent and high-quality coffee aroma. The coffee roasting process was analyzed by direct injection of the roaster gas into a time-of-flight mass spectrometer and ionized either by resonance enhanced multiphoton ionization (REMPI) at 266 and 248 nm or vacuum ultraviolet single-photon ionization (VUV-SPI) at 118 nm. The VUV ionization scheme allows detecting mainly the most volatile and abundant compounds of molecular mass below 100 m/z, while REMPI ionizes mainly aromatic compounds of molecular mass larger than 100 m/z. Combining the compounds ionized by resonant and single-photon ionization, approximately 30 volatile organic compounds are monitored in real time. Time-intensity profiles of 10 important volatile coffee compounds were discussed in connection with their formation chemistry during roasting. Applying multivariate statistics (principle component analysis) on time-intensity traces of nine volatile coffee compounds, the roasting degree could be traced as a consistent path in the score plot of the two most significant principle components (including 68% of the total variance), for a range of roasting temperatures (200-250 degrees C).

The formation of 4-vinylguaiacol, guaiacol, and phenol during coffee roasting was monitored in real-time, using resonance enhanced multiphoton ionization and time-of-flight mass spectrometry. A model is proposed, based on two connected reaction channels. One channel, termed the “low activation energy” channel, consists of ester hydrolysis of 5-FQA followed by decarboxylation of the ferulic acid to form 4-vinylguaiacol, and finally polymerization at the vinyl group to form partly insoluble polymers (coffee melanoidins). The second “high activation energy” channel opens up once the beans have reached higher temperatures. It leads to formation of guaiacol, via oxidation of 4-vinylguaiacol, and subsequently to phenol and other phenolic VOCs. This work aims at developing strategies to modify the composition of coffee flavor compounds based on the time−temperature history during roasting. Keywords: Coffee; aroma; roasting; real-time analysis; mass spectrometry; resonant laser ionization

Recently we introduced a dynamic approach to determine Henry’s law constants (HLCs) of volatile organic compounds (VOCs) in water, and applied it to a series organic compounds dissolved in pure water. Here, we first discuss a further development of the original approach such that it can be applied to complex liquid food systems (coffee). Second, we examine the impact of non-volatile constituents on the HLC. More specifically, we evaluate the impact of non-volatile coffee constituents on the HLC of 2-methylpropanal, 3- and 2-methylbutanal, dimethylsulfide, dimethyldisulfide and ethyl-2-methylbutyrate. Finally, we demonstrate that the concentration on the VOC in solution does not affect the HLC, over the investigated concentration range of 10−4 to 10 ppm.

Aroma is central to a pleasurable eating/drinking experience but is one of the most labile components of food. Coffee is an outstanding example. Attempts to avoid or control aroma degradation are often frustrated by ignorance of the microscopic mechanisms that are responsible for it. One of the processes most frequently invoked is radical formation, yet the identity of the radicals and their involvement in aroma degradation are poorly understood at the molecular level. Here a step forward in the fundamental understanding of this complex problem is taken by identifying the most relevant radicals and their products using first-principles calculations. Over 100 radicals originating from key aroma compounds found in coffee and other foods have been studied and classified according to an unambiguous criterion: their thermodynamic stability relative to common radical sources. This classification scheme predicts that most aroma molecules are resistant to both peroxidation and attack from phenolic antioxidants but are unstable with respect to radicals such as •OH. Dimers – generated from radical reactions – were also considered, and the most volatile species, which may further contribute to coffee aroma degradation, were focused on. Those – which are very few indeed – that have this potential have been identified.

An extensive analysis of the headspace (HS) of coffee brew using proton-transfer-reaction mass-spectrometry (PTR-MS) is presented. In particular, we present a set of methods that link mass spectral peaks, as observed in PTR-MS, to chemical compounds in the HS of coffee. Combining all this information, a tentative assignment and rough quantification of liquid coffee HS is presented. Coffee was chosen because it contains a large number of chemically diverse volatile organic compounds (VOCs), representing a challenging system for on-line analysis by PTR-MS.

EPR spectra of soluble coffee display single-line free radical signals in both the solid state and aqueous solution, along with signals from the paramagnetic ions Fe(III) and Mn(II). The intensity of the free radical signal in the pure solid was estimated to be ca. 7.5 x 10(16) unpaired electrons/g, and there was no significant change on dissolution in water. In aqueous solutions, however, the free radical signal declined rapidly over ca. 10-15 min in the temperature range 20-65 degrees C, after which only slow changes were observed. This decline, which was essentially independent of atmosphere, was greatest for the lowest temperatures used, and the intensity after 1 h fitted well to an exponential curve with respect to temperature. The free radicals responsible for the single-peak EPR signal did not react with any of the spin traps tested in the present experiments, but unstable free radicals with parameters consistent with adducts of C-centered radicals were detected in coffee solutions in the presence of PBN and 4-POBN spin traps. The presence of oxygen in the solutions increased the initial rate of formation of these free radical adducts. No adducts were detected when DEPMPO was used as spin trap. However, *OH adducts of DEPMPO were shown to be unstable in the presence of coffee, a fact which illustrates the strong free radical scavenging ability of coffee solutions.

The stability of the coffee flavor compound furfuryl mercaptan has been investigated in aqueous solutions under Fenton-type reaction conditions. The impact of hydrogen peroxide, iron, ascorbic acid, and ethylenediaminetetraacetic acid was studied in various combinations of reagents and temperature. Furfuryl mercaptan reacts readily under Fenton-type reaction conditions, leading to up to 90% degradation within 1 h at 37 degrees C. The losses were lower when one or more of the reagents was omitted or the temperature decreased to 22 degrees C. Volatile reaction products identified were mainly dimers of furfuryl mercaptan, difurfuryl disulfide being the major compound. In addition, a large number of nonvolatile compounds was observed with molecular masses in the range of 92-510 Da. The formation of hydroxyl and carbon-centered radicals was indicated by electron paramagnetic resonance spectra using alpha-(4-pyridyl-1-oxide)-N-tert-butylnitrone or 5-(diethoxyphosphoryl)-5-methyl-1-pyrroline-N-oxide as spin traps. Whereas *OH was generated by Fenton-type reactions, the C-centered radical is probably a secondary product of the reaction of *OH with various organic molecules, the reaction with furfuryl mercaptan appearing to be the most important. No evidence for S-centered radicals was seen in the spin-trapping experiments, but a sulfur-containing radical was detected when measurements were made at 77 K in the absence of spin traps.

Erworben im Rahmen der Schweizer Nationallizenzen (http://www.nationallizenzen.ch), Volatile organic compounds (VOCs), emitted from green coffee beans, during coffee roasting and from a cup of coffee, were all analysed by proton-transferreaction mass spectrometry. Firstly, the headspace (HS) of green beans was investigated. Alcohols dominate the HS, but aldehydes, hydrocarbons and organic acids were also abundant. Secondly, we roasted coffee under two different conditions and monitored on-line the VOCs emitted during the process. In a first roasting series, a batch of beans was roasted. After an initial drying phase, dominated by evaporation of water and methanol, the HS concentrations of VOCs such as acetic acid, acetaldehyde, pyridine and methylbutanal rapidly increased and went through a maximum at medium roast level. In a second series, just six beans were roasted. We observed sporadic bursts of some volatiles (furans, butanal, 2,3- pentanedione), coinciding with popping sounds. Other VOCs showed smooth time-intensity profiles (pyridine, pyrazine). These experiments gave a real-time insight into the complex processes taking place during roasting. Finally, the HS of coffee extracts, prepared from beans roasted to different roast levels, were analysed. Most VOCs showed a maximum concentration at medium roast level (e.g. pentanedione, furfural, 5-methyl furfural), while others showed a gradual increase (e.g. pyrrol) or decrease (e.g. methanol).

In the 1990s we began to understand that free radical damage is involved in artery-clogging atherosclerosis and health problems like vision loss, cancer or chronic diseases. Studies have shown that the damage especially affects people with a low consumption of antioxidant-rich fruits, vegetables...and coffee. Is this just a fairy tale promoted by the coffee industry? Scientists at the Zurich University of Applied Sciences (ZHAW) in Wädenswil wanted to get to the bottom of the question.

Flavour research is a demanding domain in terms of analytical methodology as key odorants usually occur in trace amounts, often embedded in extracts containing volatile compounds at much higher concentrations. Since its early days, GC-MS has been a key tool in flavour laboratories enabling characterisation of thousands of volatile components in food products. However, as flavour chemists delve deeper into the understanding of flavour generation and delivery, there is a need for more powerful methodologies adapted to their specific needs. This paper will present two techniques that allow flavour separation and characterisation, namely GC-TOFMS and MS/MS. Moreover, APCI-MS, PTR-MS and REMPI-TOFMS will be discussed as they enable direct investigation of volatile compounds without any chromatographic step, thus studying release of flavour compounds during food processing or food consumption.

Erworben im Rahmen der Schweizer Nationallizenzen (http://www.nationallizenzen.ch), The aromas of a reference green Mexican coffee (Arabica) and of a coffee from the same origin, but having a pronounced earthy/mouldy off-taint, were characterised. From comparison of the two aroma profiles, the compounds causing the defect were detected by gas chromatography olfactometry, isolated and concentrated by preparative bi-dimensional gas chromatography, and characterised by gas chromatography mass spectrometry. Six compounds participated in the off-flavour. Geosmin, 2-methylisoborneol, 2,4,6-trichloroanisole were found to be the main culprits, while three methoxy pyrazines (2-methoxy-3-isopropyl/-3-sec-butyl/-3-isobutyl pyrazine) contributed to a lesser extent to the earthy/ green undertone. The occurrence of the off-flavour could tentatively be linked to post-harvest drying.

REMPI@266nm-TOFMS is used for on-line analysis of the coffee roasting process. Volatile and flavor active compounds of coffee were ionized by REMPI@266nm and monitored on-line and in real-time by TOFMS during the coffee roasting process. The phenol and 4-vinylguaiacol time-intensity profiles, for example, show typical behavior for different roasting temperatures and provide an indicator to the achieved degree of roasting. The impact of the moisture level of the green coffee beans on the time shift of a typical (commercial) roasting time, correlates with REMPI-TOFMS measurements and literature data.

The technique of carbon-arc evaporation has been successfully utilized to encapsulate a wide variety of rare-earth species in carbon cages. The authors have observed M{sub m} @ C{sub n} (M = Ce, Nd, Sm, Eu, Gd, Tb, Dy, Ho, or Er) species present in the toluene extracts of the carbon soot using laser desorption mass spectrometry. The presence of multiple-metal species appears to depend strongly on the metal-to-carbon atom ratio found in the starting rods, with the higher metal concentrations favoring multiple-metal incorporation. One often observed dimetallofullerene is M{sub 2}{degrees}C{sub 80}. Molecular orbital arguments are presented to support a possible icosahedral structure for C{sub 80}. 27 refs., 2 figs., 1 tab.

Using REMPI@266 nm or 248 nm several phenolic compounds, such as Phenol or the flavor-active 4-vinylguaiacol, can be detected in the roast off-gas.

Resonance-enhanced multi-photon ionization time-of-flight mass spectrometry (REMPI/TOFMS) has been applied to the detection of volatiles in the headspace of brewed coffee and in the coffee roasting process-gas. A frequency quadrupled Nd:YAG laser (266 nm) was used for REMPI ionization (REMPI@266nm) of the volatiles in an effusive molecular beam inside the ion source of a linear TOF mass spectrometer. A special sampling system provided a time correlated sampling. Under these circumstances REMPI@266nm is highly selective for ionization of phenolic compounds. Several phenolic compounds, such as the flavour-active 4-vinylguaiacol, can be detected in the headspace of coffee brew as well as in the roast off-gas with the application of this approach. Moreover, the nitrogen heterocyclic compounds, indole and caffeine, were detected in both cases. During the roasting process the relative changes in concentration of some volatile components of coffee have been recorded by EMPI@266nm with a time resolution of 1 Hz. The different volatiles exhibit characteristic concentration profiles as a function of the roast time. These results demonstrate the applicability of REMPI-TOFMS for on-line monitoring of coffee processing technologies. Such an on-line monitoring technique is of particular interest for process-control purposes, e.g. quality-protection or feedback process control. For example, monitoring of off-gases from the coffee roast process or monitoring of certain unit operations during the instant-coffee manufacturing could be promising industrial applications.

Density functional studies of the abundant cluster Na6Pb and of its analogue Na6Mg are reported. The structure of Na6Pb has been optimized for a series of symmetry constraints (Oh, D3d, D3h, C5v, C3v and C2v). The resulting binding energies fall within a narrow range of less than 0.1 eV whereas a spread of more than 0.5 eV is calculated for Na6Mg. These findings indicate a high structural flexibility of Na6Pb. The Pb atom exhibits a propensity to occupy a highly coordinated site in contrast to Mg which, in the most stable structures, is attached to the ‘outside’ of a Na6 moiety. Analysis of the bonding mechanism revealed two major contributions which increase the atomization energy of Na6Pb compared to Na6Mg: an enhanced charge transfer from the Na6 subsystem and a stronger polarization of the Pb atom. A significant contribution to the overall cluster stability comes from the interaction between the alkali atoms.

Recently we reported on vibrationally resolved spectra of the ionic ground state of Ag 2 + via ZEKE spectroscopy. The vibronic intensity distributions could not be interpreted within the Franck-Condon scheme. Here, we show that it is possible to overcome this discrepancy by invoking the breakdown of the Born-Oppenheimer approximation in the ZEKE states of silver dimer. A comparison of the spectral structure of the direct ion signal with simultaneously recorded ZEKE band profiles further illustrates this non-Franck-Condon behavior.

Mass-spectral results on alkali clusters containing one host-atom with ns2 valence-shell configuration (Mg, Ca, Sr, Ba, Zn, Eu, and Yb) are presented. They allow uncoupling of the number of atoms in the cluster from the number of its valence electrons by probing with elements with more than one valence electron and different ionization potential and atomic radius. Prominent intensity maxima for specific cluster sizes are observed. Based on an electronic shell model, a systematic interpretation of the intensity maxima as a function of the incorporated heteroatom is presented. Although most of the gross features can be rationalized within a purely electronic model, a more refined analysis prompts one to geometric structure effects which have to be included to more fully describe the spectra.

We report on mass-analyzed ZEKE spectra of Ag+2 via resonance-enhanced two-color excitation. To the best of our knowledge, this is the first metal dimer and at the same time the heaviest system (218 amu) ever investigated by mass-analyzed ZEKE. The adiabatic ionization potential, vibrational energies for v+ = 1, 2, 3 and 4 as well as the vibrational constants ωe, ωeχe of the ionic ground state X2Σ+g are determined with high accuracy. The surprising intensity pattern of vibrational progressions cannot be rationalized within a Franck—Condon picture and points to the unique properties of ZEKE states.