Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Evaluation of Ozone Removal by Spent Coffee Grounds


Activated carbon is the most known material used to adsorb ozone. Activating carbonaceous materials by ozonation is commonly used to produce activated carbon, however, requiring sophisticated skills and professional equipment. This paper presents a reversed idea: to adsorb ozone using an unactivated carbonaceous material, coffee. Three powder adsorbents are presented: fresh coffee (unactivated), spent coffee grounds (unactivated), and activated carbon (commercially available). The test is conducted by measuring and comparing the ozone concentration in an ozone-supplied chamber with or without the ozone adsorbent. The results show that, at the specific conditions, the peak ozone concentration is lowered by 38% to 56% when the chamber has the activated carbon. At the same conditions, the peak ozone concentration is lowered by 25% to 43% when the chamber has the coffee powders (either fresh or spent). The elemental analysis demonstrates that the oxygen content after the ozone adsorption increases by 20%, 14.4%, and 34.5% for the fresh coffee, the spent coffee grounds, and the activated carbon, respectively. The characteristic analysis (the Fourier-transform infrared spectroscopy, the thermogravimetric, and the Brunauer-Emmett-Teller) suggests that the unactivated coffee is not porous, however, contains various organic compounds that could react with and consume ozone.


Ozone (O3) is smell-irritating, colorless, capable of oxidizing organic compounds, and one of the six criteria air pollutants set by the United States Environmental Protection Agency. Besides, ozone is able to react with terpenoids to form secondary organic aerosols1,2 that take a significant mass fraction of aerosol particles3. Long-term exposure to an unconditioned ozone environment can cause health problems such as asthma, allergic, airway issues, and even mortality4,5,6. To maintain air quality and to protect people, several countries have set the regulations of the maximum ozone concentration7,8.

Chemically, ozone is formed when an oxygen atom (O) attaches to an oxygen molecule (O2). However, ozone is unstable and the depletion of ozone is spontaneous in nature. Simply, the formation and the depletion of ozone are shown in Eq. (1) to Eq. (3).

$${\rm{e}}+{{\rm{O}}}_{2}\to 2{\rm{O}}\,\cdot +{\rm{e}}$$
$${\rm{O}}\,\cdot +{{\rm{O}}}_{2}\to {{\rm{O}}}_{3}$$
$${\rm{O}}\,\cdot +{{\rm{O}}}_{3}\to 2{{\rm{O}}}_{2}$$

Because of many known adverse health effects, controlling ozone concentration is required for certain environments such as aircraft cabins9 and offices/buildings that come with discharge-based devices10, e.g., laser printers11 and electrostatic precipitators12. Activated carbon is one of the commonly used ozone adsorbents because of its large surface area and specific chemical properties. Mueller et al. showed that applying the activated carbon filter in an 11.9 m3 aluminum room where has a working electric air cleaner lowers the ozone concentration by 90% in seven minutes13. Yang et al. presented a novel technique that combines the carbon nanotubes and the activated carbon filter to remove ozone and reported a removal efficiency of 99%14.

Activated carbon can be produced by chemically or physically activating carbonaceous materials such as coal, peat, rice husk, wood, and peach stone15,16,17. Coffee, one of the most common daily drinks in modern society, is essentially carbonaceous as well. A few researchers have successfully turned the coffee into the activated carbon. Boonamnuayvitaya et al. made the activated carbon from the coffee residues with the different activating agents and reported that the maximum specific surface area was about 914 m2 g−118. Kante et al. made the activated carbon from the spent coffee waste with an agent of zinc chloride under several treatment conditions, and the maximum specific surface area presented was up to 1,121 m2 g−119. Namane et al. demonstrated that the coffee-grounds made activated carbon has a promising removal efficiency for the phenol (>80%) and the dye (>90%) when compared to the commercial activated carbon20.

It is certain that activated carbon is capable of adsorbing ozone and can be made from spent coffee grounds by proper activation processes that, however, require sophisticated skills and professional equipment. This paper presents an idea to adsorb ozone by using two types of unactivated coffee powder: fresh coffee and spent coffee grounds. The commercially available activated carbon powder is also introduced for the comparison purpose. This paper presents the ozone concentration and ozone removal efficiency when there present the mentioned adsorbents in a chamber. Four characteristic analysis are then brought out to see how the coffee powders react with ozone, including the energy-dispersive X-ray spectroscopy (EDS), the Fourier-transform infrared spectroscopy (FTIR), the thermogravimetric analysis (TGA), and the specific surface area (Brunauer-Emmett-Teller, BET).

Material and Methods

The experimental setup includes three components connected in series. The ozone generator provides the ozone flow to a chamber that connects to an ozone analyzer (Ecotech Serinus 10) used to measure the ozone concentration. The ozone adsorbent under test is placed in the chamber to react with ozone.

Ozone generator

A dielectric barrier discharge based ozone generator is used to provide a stable ozone flow21,22. The ozone generator consists of an aluminum cylinder (electrode) and a quartz tube (dielectric material). A pump is used to supply air to the ozone generator at a constant rate of 4 × 10−5 m3 s−1 (2.4 liters per minute).


The chamber is made of 10-mm-thick transparent acrylic plates, as shown in Fig. 1. The exterior dimension of the chamber is 500 mm by 500 mm by 200 mm. There are four openings on the walls of the chamber. One is the ozone inlet (at the center of the wall), the one right opposite to the ozone inlet connects to the ozone analyzer, while the remaining two are open to the atmosphere to balance the flow and the pressure. The ozone adsorbent is placed in a shallow basin in the bottom center of the chamber.

Figure 1

The schematic and the dimension of the chamber.

Ozone adsorbent


This paper tests three powder adsorbents: fresh coffee, spent coffee grounds, and activated carbon. Table 1 summarizes the information and the conditions of these adsorbents. Note that all the coffee powders used in this paper are unactivated.

Table 1 The information and the conditions of the three ozone adsorbents.

All these powder adsorbents are prepared by grinding their fresh beans using the same grinder (Cuisinart DBM-8TW) at the same size setting (Medium). The spent coffee grounds are the wastes of brewing the fresh coffee powder by a regular coffee machine (Frigidaire FKC1151HS). Before getting tested, the spent coffee grounds are baked in an oven at 100°C for 6 hours.

To understand if the amount of the ozone adsorbent would affect the performance of the ozone removal, this paper tests the adsorbent at two weights. When the amount of the ozone adsorbent is 100 grams, one-third of the shallow basin (close to the ozone inlet) is evenly filled with the ozone adsorbent, while the remaining two-thirds is placed with the acrylic plates. When the amount of the ozone adsorbent is 300 grams, the entire shallow basin is evenly filled with the ozone adsorbent. Note that the entire shallow basin is placed with the acrylic plates when conducting the test that is without any ozone adsorbent.

Physical inspections

Figure 2 shows the particle size distribution in terms of equivalent sphere diameters using a particle size analyzer (Malvern Mastersizer 2000) and the shape inspection using a scanning electron microscope (SEM, JEOL JSM-6390LV).

Figure 2

The particle size distribution of the three ozone adsorbents.

Although the particle size distribution of these three ozone adsorbents is similar, the fresh coffee and the spent coffee grounds have some large debris. The spent coffee grounds have the largest volume-weighted mean diameter probably because some of the debris agglomerates to the bigger ones. On the other hand, the activated carbon bean has a higher Young’s Modulus and is thus more brittle when compared with the coffee bean23, making the activated carbon powder finer. Moreover, the SEM images show that the shape of all the ozone adsorbents is irregular, as expected.

Procedures for measuring ozone concentration

The ozone analyzer measures and records the ozone concentration of the chamber every 10 seconds and nonstop for 23 minutes, while the ozone generator turns on only for the first three minutes and then turns off. Note that although the ozone generator shuts down exactly at the third minute, the ozone concentration of the chamber read by the ozone analyzer still increases for another half a minute. This is because the chamber is big and the ozone analyzer needs some time to read the ozone concentration that represents the one after the ozone generator is turned off. In order to ensure the repeatability, five measurements are conducted for every testing leg.

Procedures for conducting characteristic analysis

This paper inspects the ozone adsorbent by the FTIR, the TGA, and the BET to identify the changes before and after the ozone adsorption.

For the FTIR analysis, the sample (ozone adsorbent) of one milligram is first dried out completely, and then, is mixed with 100 mg potassium bromide (KBr) to make a pellet. The pellet is compressed by a heavy hydraulic jack (12 Ton E-Z PressTM) at 10 ton cm−2 to make a thin film. The thin film sample is then analyzed immediately using the FTIR spectroscopy (Bio-Rad FTS-3500) to avoid possible humidity issues. The background spectrum is obtained using a pure KBr pellet by the same mass and the same manner mentioned above. The FTIR results are presented by the spectrums that are subtracted the background ones from the sample ones to highlight the changes.

The TGA analysis is carried out by the thermogravimetric analyzer (TA Instruments TGA Q500). One gram sample is heated in the temperature range of 0°C to 800°C at a rate of 20 °C min−1 under an airflow.

Before getting tested in the BET analyzer (MicrotracBEL BELSORP-max) with nitrogen, the sample is heated up to 150°C under a vacuum condition (<10−2 kPa) for four hours (MicrotracBEL BELPREP-vac II) in order to be completely dehydrated. The nitrogen adsorption-desorption isotherms are logged at 77 K. The specific surface area is calculated by the BET method, while the total pore volume is got based on the amount of the nitrogen adsorbed at a 0.99 relative pressure.

Results and Discussion

Ozone concentration

Figure 3 shows the ozone concentrations of the chamber over time, while the peak ozone concentrations are numerically labeled.

Figure 3

The ozone concentrations over time with and without the ozone adsorbent. The peak ozone concentrations are marked accordingly.

During the ozone generation period (before the 3rd minute), when the chamber comes with the ozone adsorbents, the rate of the ozone generation is not as linear as the case that comes without the ozone adsorbents, and the ozone concentration is thus suppressed. It is also apparent that the more the ozone adsorbents are presented in the chamber, the stronger the effects of the ozone suppression are. This is because when the chamber has more adsorbents, there are more surface areas that can react with ozone.

Although the fresh coffee, the spent coffee grounds, and the activated carbon do react with ozone, the capabilities of the ozone suppression of the fresh coffee and the spent coffee grounds look similar while the activated carbon works best as anticipated. The peak ozone concentration (at the 3.5th minute) is lowered by 26.4%, 24.4%, and 38.3% when the chamber presents 100 grams of the fresh coffee, the coffee ground, and the activated carbon, respectively. Furthermore, the peak ozone concentration is lowered by 43.8%, 42.3%, and 55.7% when the chamber presents 300 grams of the fresh coffee, the coffee ground, and the activated carbon, respectively.

Ozone removal efficiency

Figure 4 shows the time-dependent ozone removal efficiency ηremoval defined by Eq. (4), for the ozone depletion period (after the 3.5th minute).

$${\eta }_{{\rm{removal}}}=1-\frac{{C}_{{\rm{t}}}(t)}{{C}_{{\rm{i}}}}$$

where Ci is the initial ozone concentration and Ct(t) is the ozone concentration with respect to time.

Figure 4

The ozone removal efficiency over time with and without the ozone adsorbent.

All the ozone adsorbents do speed up the ozone removal, but the rate of the ozone removal declines and saturates over time. This is because the ozone desorption phase in a chamber theoretically decays over time in an exponential manner24 and the adsorption capability of a substance has a cap25.

On the other hand, Fig. 4 also shows that the spent coffee grounds work as good as the fresh coffee, even better when the amount is low. This is because ozone is water-soluble, while the spent coffee grounds used in this case still contains some water. Such the results give one more reason to recycle the spent coffee grounds for ozone removal. Note that the mean diameters of these three adsorbents are different such that the results shown in Fig. 4 may favor the activated carbon because of its small mean diameter. In other words, if the mean diameter of the spent coffee grounds could be as small as that of the fresh coffee or even as that of the activated carbon, the capability of the ozone removal of the spent coffee grounds could be higher.

Characteristic analysis

Elemental analysis

Table 2 shows the elemental analysis by an EDS (JEOL JSM-6390LV). The majority of the elements of all the ozone adsorbents is carbon, and the percent weight of carbon does not change too much after adsorbing ozone (from 1.1% to 2.1%). The increasing of the oxygen after the ozone adsorption gives a clue that these three adsorbents do react with ozone, while the activated carbon changes the most and the spent coffee grounds change the least.

Table 2 The EDS results for the three ozone adsorbents before and after the ozone adsorption.

FTIR analysis

Figure 5 shows the analysis of all the ozone adsorbents before and after the ozone adsorption using the FTIR spectroscopy to check if there are any changes in the functional groups.

Figure 5

The FTIR results for the three ozone adsorbents (arbitrary adsorbance-axis).

The fresh coffee and the spent coffee grounds have nearly identical spectrums before and after the ozone adsorption. In other words, the functional groups of both the coffees are not chemically modified much after reacting with ozone for 23 minutes. On the contrary, the activated carbon has dramatically different spectrums before and after the ozone adsorption. This implies that the functional groups of the activated carbon have chemically changed after the ozone adsorption, coincidence with those reported in the literature25,26,27.

Furthermore, the most significant difference in the band between the coffees (both fresh coffee and spent coffee grounds) and the activated carbon is that the coffees have three major peaks (1745 cm−1, 2860 cm−1, and 2930 cm−1) and one minor peak (3390 cm−1) while the activated carbon does not. The types of vibrations responsible for the peaks mentioned above are C=O stretching, C–H stretching (aliphatic), and O–H/N–H stretching28. Such a difference indicates that the coffee comprises of many organic compounds that are highly oxidative29. This is believed to be one of the reasons that coffee helps consume ozone.

TGA analysis

The TGA analysis is to examine the pyrolytic behaviors of the ozone adsorbents. In general, there are three thermal stages for organic substances. The first stage is water removal. The second stage could consist of several sub-stages that associate with different chemical decompositions. The last stage is the complicated changes in the structure of the lignin. Figure 6 shows the TGA results for all the three ozone adsorbents.

Figure 6

The TGA results for the three ozone adsorbents.

It is not surprising that the results of the activated carbon agree well with those reported in the literature30,31. The following observations and the explanations are made to both the fresh coffee and the spent coffee grounds because they have similar behaviors. The water removal stage happens before ~200°C, during which ~8% of the weight is removed in this stage. The following two sub-stages that reduce 70% to 90% of the weight could be the thermal depolymerization of hemicelluloses and cellulose degradations32. In other words, these two sub-stages are the carbonization stage33, suggesting that the coffee is an organic compound rich substance. The last stage starts around ~500°C to ~550°C, turning the remaining mass into ashes.

BET analysis

This paper also evaluates the specific surface area and the total pore volume of all the testing ozone adsorbents using a BET analyzer, while the results are shown in Table 3. For the activated carbon after the ozone adsorption, the specific surface area and the total pore volume decrease, similar to the results reported in the literature34. For the unactivated coffee, both fresh and spent, the specific surface area is three orders smaller and the total pore volume is four orders smaller than those of the activated carbon. Therefore, unactivated coffee can be considered non-porous.

Table 3 The results of the BET analysis.

Before the ozone adsorption, both the specific surface and the total pore volume of the fresh coffee are larger than those of the spent coffee grounds. This is probably because the spent coffee grounds are water-reacted coffee powders such that some compounds might be formed, changing the amount of the surface area and the pore volume when compared with the fresh coffee.

After ozone adsorption, the specific surface area and the total pore volume of both types of coffee decrease, meaning that the pores of these two types of coffee are obstructed, physically or chemically. While the decreasing rates of both the specific surface area and the total pore volume of the fresh coffee are larger than those of the spent coffee grounds, the capability of the ozone adsorption of the spent coffee grounds is as good as that of the fresh coffee. A possible reason causing the above phenomena could also be the water content in the spent coffee grounds. The spent coffee grounds are not dried out before getting tested, while ozone is water-soluble. In other words, although water occupies some pores in the spent coffee grounds, water also helps dissolve ozone, making the spent coffee grounds adsorb ozone as good as the fresh coffee does.


This paper presents how the unactivated coffee powder helps ozone removal. The results show that having some fresh coffee or spent coffee grounds in an ozone-supplied chamber does suppress the ozone concentration by up to 43%, competitive to the performance of the commercial activated carbon (about 56%). Recycling spent coffee grounds to remove ozone could be further developed for specific purposes.

The characteristic analysis suggests that unactivated coffee is not highly porous but is an organic compound rich material. The FTIR analysis shows that the unactivated coffee contains a certain amount of hydrocarbon bonds that are the characteristics of organic compounds. Besides, the surface functional groups of the unactivated coffee do not change too much before and after the ozone adsorption because the FTIR spectrums do not change significantly. The TGA analysis indicates that the unactivated coffee has a clear carbonization stage, the proof of its unactivated characteristic and thus organic compound rich. On the other hand, the BET analysis demonstrates that the unactivated coffee is not as porous as the activated carbon is. The BET results also show that both the specific surface area and the total pore volume of the unactivated coffee significantly decrease after the ozone adsorption, implying that something created by the reactions between the ozone and the unactivated coffee obstructs the pores of the unactivated coffee.


  1. 1.

    Coleman, B. K., Lunden, M. M., Destaillats, H. & Nazaroff, W. W. Secondary organic aerosol from ozone-initiated reactions with terpene-rich household products. Atmos. Environ. 42, 8234–8245 (2008).

    ADS  CAS  Article  Google Scholar 

  2. 2.

    Li, T., Blande, J. D. & Holopainen, J. K. Atmospheric transformation of plant volatiles disrupts host plant finding. Sci. Rep. 6, 33851 (2016).

    ADS  CAS  Article  Google Scholar 

  3. 3.

    Baltensperger, U. et al. Combined determination of the chemical composition and of health effects of secondary organic aerosols: The POLYSOA project. Journal of Aerosol Medicine and Pulmonary Drug Delivery 21, 145–154 (2008).

    CAS  Article  Google Scholar 

  4. 4.

    Sheffield, P. E., Zhou, J., Shmool, J. L. C. & Clougherty, J. E. Ambient ozone exposure and children’s acute asthma in New York City: a case-crossover analysis. Environmental Health 14, 25 (2015).

    Article  Google Scholar 

  5. 5.

    Salonen, H., Salthammer, T. & Morawska, L. Human exposure to ozone in school and office indoor environments. Environ. Int. 119, 503–514 (2018).

    CAS  Article  Google Scholar 

  6. 6.

    Hata, H. & Tonokura, K. Impact of next-generation vehicles on tropospheric ozone estimated by chemical transport model in the Kanto region of Japan. Sci. Rep. 9, 3573 (2019).

    ADS  Article  Google Scholar 

  7. 7.

    Wen, T. Y. High-efficiency electrostatic precipitators PhD Dissertation thesis, University of Washington (2015).

  8. 8.

    Lange, S. S. Comparing apples to oranges: Interpreting ozone concentrations from observational studies in the context of the United States ozone regulatory standard. Sci. Total Environ. 644, 1547–1556 (2018).

    ADS  CAS  Article  Google Scholar 

  9. 9.

    Gao, K., Xie, J. & Yang, X. Estimation of the contribution of human skin and ozone reaction to volatile organic compounds (VOC) concentration in aircraft cabins. Build. Environ. 94, 12–20 (2015).

    Article  Google Scholar 

  10. 10.

    Jung, J. S. & Moon, J. D. Corona discharge and ozone generation characteristics of a wire-plate discharge system with a glass-fiber layer. J. Electrostat. 66, 335–341 (2008).

    CAS  Article  Google Scholar 

  11. 11.

    Barrese, E. et al. Indoor pollution in work office: VOCs, formaldehyde and ozone by printer. Occupational Diseases and Environmental Medicine 2, 49 (2014).

    Article  Google Scholar 

  12. 12.

    Tanasomwang, L. & Lai, F. C. Long-term ozone generation from electrostatic air cleaners. Industry Applications Conference 3, 2037–2044 (1997).

    Google Scholar 

  13. 13.

    Mueller, F. X., Loeb, L. & Mapes, W. H. Decomposition rates of ozone in living areas. Environ. Sci. Technol. 7, 342–346 (1973).

    ADS  CAS  Article  Google Scholar 

  14. 14.

    Yang, S., Zhu, Z., Wei, F. & Yang, X. Carbon nanotubes/activated carbon fiber based air filter media for simultaneous removal of particulate matter and ozone. Build. Environ. 125, 60–66 (2017).

    Article  Google Scholar 

  15. 15.

    Wigmans, T. Industrial aspects of production and use of activated carbons. Carbon 27, 13–22 (1989).

    Article  Google Scholar 

  16. 16.

    Sugashini, S. & Begum, K. M. M. S. Preparation of activated carbon from carbonized rice husk by ozone activation for Cr (VI) removal. Carbon 93, 1086–1087 (2015).

    Article  Google Scholar 

  17. 17.

    Maponga, T. C. & Mahamadi, C. Efficient Au(CN)2-12 adsorption using peach stone-derived granular activated carbon. Sci. Rep. 9, 3373 (2019).

    ADS  Article  Google Scholar 

  18. 18.

    Boonamnuayvitaya, V., Sae-ung, S. & Tanthapanichakoon, W. Preparation of activated carbons from coffee residue for the adsorption of formaldehyde. Sep. Purif. Technol. 42, 159–168 (2005).

    CAS  Article  Google Scholar 

  19. 19.

    Kante, K., Nieto-Delgado, C., Rangel-Mendez, J. R. & Bandosz, T. J. Spent coffee-based activated carbon: specific surface features and their importance for H2S separation process. J. Hazard. Mater. 201, 141–147 (2012).

    Article  Google Scholar 

  20. 20.

    Namane, A., Mekarzia, A., Benrachedi, K., Belhaneche-Bensemra, N. & Hellal, A. Determination of the adsorption capacity of activated carbon made from coffee grounds by chemical activation with ZnCl2 and H3PO4. J. Hazard. Mater. 119, 189–194 (2005).

    CAS  Article  Google Scholar 

  21. 21.

    Eliasson, B., Hirth, M. & Kogelschatz, U. Ozone synthesis from oxygen in dielectric barrier discharges. J. Phys. D: Appl. Phys. 20, 1421 (1987).

    ADS  CAS  Article  Google Scholar 

  22. 22.

    Kogelschatz, U. Dielectric-barrier discharges: their history, discharge physics, and industrial applications. Plasma Chem. Plasma Process. 23, 1–46 (2003).

    CAS  Article  Google Scholar 

  23. 23.

    Lee, H. K., Park, Y. G., Jeong, T. & Song, Y. S. Green nanocomposites filled with spent coffee grounds. J. Appl. Polym. Sci. 132, 42043 (2015).

    Google Scholar 

  24. 24.

    Yu, K. P., Lee, G. W. M., Hsieh, C. P. & Lin, C. C. Evaluation of ozone generation and indoor organic compounds removal by air cleaners based on chamber tests. Atmos. Environ., 45 (2011).

  25. 25.

    Valdes, H., Sanchez-Polo, M., Rivera-Utrilla, J. & Zaror, C. A. Effect of ozone treatment on surface properties of activated carbon. Langmuir 18, 2111–2116 (2002).

    CAS  Article  Google Scholar 

  26. 26.

    Chiang, H. L., Huang, C. P. & Chiang, P. C. The surface characteristics of activated carbon as affected by ozone and alkaline treatment. Chemosphere 47, 257–265 (2002).

    ADS  CAS  Article  Google Scholar 

  27. 27.

    Subrahmanyam, C., Bulushev, D. A. & Kiwi-Minsker, L. Dynamic behaviour of activated carbon catalysts during ozone decomposition at room temperature. Appl. Catal., B 61, 98–106 (2005).

    CAS  Article  Google Scholar 

  28. 28.

    Socrates, G. Infrared and Raman characteristic group frequencies: tables and charts. 3rd edn, (John Wiley and Sons, 2004).

  29. 29.

    Rivera-Utrilla, J. & Sanchez-Polo, M. Ozonation of 1, 3, 6-naphthalenetrisulphonic acid catalysed by activated carbon in aqueous phase. Appl. Catal., B 39, 319–329 (2002).

    CAS  Article  Google Scholar 

  30. 30.

    Suarez-Ojeda, M. E. et al. Catalytic wet air oxidation of substituted phenols using activated carbon as catalyst. Appl. Catal., B 58, 105–114 (2005).

    CAS  Article  Google Scholar 

  31. 31.

    Amankwah, R. K., Pickles, C. A. & Yen, W. T. Gold recovery by microwave augmented ashing of waste activated carbon. Miner. Eng. 18, 517–526 (2005).

    CAS  Article  Google Scholar 

  32. 32.

    Garcia-Garcia, D., Carbonell, A., Samper, M. D., Garcia-Sanoguera, D. & Balart, R. Green composites based on polypropylene matrix and hydrophobized spend coffee ground (SCG) powder. Composites Part B 78, 256–265 (2015).

    CAS  Article  Google Scholar 

  33. 33.

    Jutakridsada, P., Prajaksud, C., Kuboonya-Aruk, L., Theerakulpisut, S. & Kamwilaisak, K. Adsorption characteristics of activated carbon prepared from spent ground coffee. Clean Technol. Environ. Policy 18, 639–645 (2016).

    CAS  Article  Google Scholar 

  34. 34.

    Alvarez, P. M., Garcia-Araya, J. F., Beltran, F. J., Masa, F. J. & Medina, F. Ozonation of activated carbons: Effect on the adsorption of selected phenolic compounds from aqueous solutions. J. Colloid Interface Sci. 283, 503–512 (2005).

    ADS  CAS  Article  Google Scholar 

Download references


The authors would like to thank Prof. Chao-Chang Chen (NTUST-ME), Prof. Pen-Chi Chiang (NTU-ENEV), Prof. Ming-Jer Lee (NTUST-ChE), Ms. Mei-Hsing Chang (NTUST-ChE), Ms. Wen-Yi Su (NTUST-ChE), and Ms. Wen-Yuan Wu (NTUST-MSE) for the equipment support and the advice on the experimental results. This work was financially supported by the High Speed 3D Printing Research Center from the Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE) in Taiwan. This work was also supported by the Ministry of Science and Technology, Taiwan (MOST 106-2221-E-011-088).

Author information




P.F.H. and T.Y.W. designed the research. P.F.H. conducted the experiments. P.F.H. and T.Y.W. interpreted the results. T.Y.W. wrote the paper.

Corresponding author

Correspondence to Tsrong-Yi Wen.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Hsieh, PF., Wen, TY. Evaluation of Ozone Removal by Spent Coffee Grounds. Sci Rep 10, 124 (2020).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing