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Article

Structural Evolution of Polyimide-Derived Carbon during Phosphoric Acid Activation

by
Alexander M. Puziy
1,*,
Olga I. Poddubnaya
1,
Barbara Gawdzik
2,
Magdalena Sobiesiak
2 and
Myroslav Sprynskyy
3
1
Department of Chemistry and Chemical Technology, National Aviation University, 1 Liubomyr Huzar Prospect, 03058 Kyiv, Ukraine
2
Department of Polymer Chemistry, Maria Curie-Skłodowska University, ul. Gliniana 33, 20-614 Lublin, Poland
3
Department of Environmental Chemistry and Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University in Torun, 7 Gagarina Str, 87-100 Torun, Poland
*
Author to whom correspondence should be addressed.
C 2022, 8(3), 47; https://doi.org/10.3390/c8030047
Submission received: 18 August 2022 / Revised: 10 September 2022 / Accepted: 14 September 2022 / Published: 19 September 2022
(This article belongs to the Special Issue Carbons for Health and Environmental Protection)
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Abstract

:
Carbon adsorbents were obtained by carbonization of polyimide polymer with and without the presence of phosphoric acid at temperatures in the range of 400–1000 °C. Carbons produced in the presence of phosphoric acid have been demonstrated to contain up to 13.2% phosphorus. The structure of phosphorus-containing compounds was investigated by XPS and 31P MAS NMR methods. Deconvolution of the P 2p peak with variable binding energy showed the presence of only phosphates/polyphosphates. However, a low value of the O/P ratio is an indirect indication of the possible presence of phosphonates. A 31P MAS NMR study revealed the existence of several kinds of phosphates as well as a minor quantity (1–9%) of phosphonates. All discovered phosphorus-containing compounds are acidic and therefore give carbon the ability to absorb metal cations. The study of copper ion adsorption demonstrated that phosphorus-containing carbon shows a significant adsorption capability even in extremely acidic conditions. At pH 3–6, phosphorus-containing carbon may completely remove copper from the aqueous solution. Phosphorus-containing carbon has a higher adsorption capacity for copper ions than ion exchange resins with carboxyl or sulfo groups.

Graphical Abstract

1. Introduction

The activation of various precursors with phosphoric acid is a widely used industrial process for the production of highly porous carbon adsorbents [1,2,3,4,5,6,7]. Phosphoric acid activation has several advantages, primarily high yields and low activation temperatures compared to physical activation [8,9,10]. In addition, phosphoric acid activation does not have the disadvantages, such as corrosion problems, insufficient recovery of the activator, and environmental problems inherent in the zinc chloride activation process [11].
Many scientists, however, are unaware of the possible inclusion of phosphorous compounds into the carbon structure during activation with phosphoric acid, which can modify the surface chemistry of the carbon adsorbent. Recently it was shown that phosphorus compounds, which are incorporated into the structure during activation with phosphoric acid, give an acidic character to the surface of activated carbon, which determines their catalytic properties and adsorption capacity for metal ions [12]. The XPS technique is most commonly used to identify the structure of phosphorus compounds in phosphorus-containing carbon materials [13,14,15,16,17]. However, there are disagreements in the literature regarding the interpretation of experimental XPS spectra, which may lead to different conclusions regarding the structure of phosphorus-containing compounds. On the one hand, some researchers conduct deconvolution of the P 2p peak with varying binding energy and assign the resulting values to specific substances with close binding energy. New peaks are added until there is no increase in the quality of fit [15,16,17,18,19,20,21,22]. On the other hand, other investigators perform deconvolution of the P 2p region to 3–4 peaks with a priori fixed binding energy values corresponding to certain phosphorus compounds [23,24,25,26,27,28]. Thus, different structures of phosphorus-containing compounds in activated carbon can be obtained from the same P 2p spectrum depending on the deconvolution scheme. The use of an auxiliary method, such as 31P NMR, can assist in identifying the structure of phosphorus compounds in carbon adsorbents and predicting their characteristics [22,29,30,31,32,33,34,35,36,37].
In this study, an analysis of the structure of phosphorus-containing compounds in activated carbons obtained from polyimides was carried out using XPS and NMR techniques and the relationship of the structure with acid-base characteristics and adsorption capacity for copper ions is established.

2. Materials and Methods

2.1. Precursor Polymer

Porous polyimide copolymer, designated as BM-DVB, was chosen as the raw material for the production of carbon adsorbents in this study. The initial BM-DVB copolymer was obtained by suspension polymerization of 4,4′-bis(maleimidodiphenyl) methane (50 mol percent) and divinylbenzene (50 mol percent) in the presence of a pore former (a mixture of decyl alcohol and benzyl alcohol) [38]. The chemical structure of BM-DVB is shown in Figure 1.

2.2. Synthesis of Carbon Adsorbents

Carbon adsorbents were obtained by carbonization of BM-DVB porous copolymer impregnated with phosphoric acid (acid/precursor ratio 1:1) at temperatures 400–1000 °C in argon flow (H3PO4 series) [39,40,41,42,43]. After carbonization, carbons were thoroughly washed with hot water in the Soxhlet extractor until the wash waters reached neutral pH. To investigate the involvement of phosphoric acid in the polymer-to-carbon transition, the second series of carbons were produced at the same temperature range without the addition of phosphoric acid (Thermal series).

2.3. Porous Structure

The porous structure of carbons was characterized by nitrogen adsorption measured at −196 °C using the Autosorb-6 adsorption analyzer (Quantachrome, Boynton Beach, FL, USA). Pore size distribution was calculated by SAIEUS software version 2.0 (www.saieus.com (accessed on 2 March 2015)) using a slit pore model incorporating surface energetical heterogeneity and geometrical corrugation [44,45,46]. The specific surface area, ABET, was calculated by the BET method using nitrogen adsorption data in the relative pressure range chosen using consistency criteria [47]. The total, Vtot, micropore, Vmi, and mesopore, Vme, volumes were calculated from the cumulative pore size distributions as the volume of pores with sizes 50 nm, less than 2 nm, and between 2 and 50 nm, respectively.

2.4. XPS

XPS spectra were obtained using a high vacuum (<8 × 10−9 mbar) multi-chamber UHV system (Prevac, Poland) equipped with Al Kα line excitation source VG Scienta SAX 100 (12 kV, 30 mA), monochromator VG Scienta XM 780 and hemispherical analyzer Scienta R4000 (VG Scienta AB, Uppsala, Sweden). The pass energy and energy steps were 200 eV and 0.5 eV at the survey spectra and 50 eV and 0.1 eV at the detailed spectra. During the measurement of carbons obtained at 400–600 °C without phosphoric acid, flooding the sample with low-energy electrons was used to neutralize the surface charge. The spectra were calibrated for a carbon C 1s excitation at a binding energy of 284.7 eV.
The spectra were analyzed and processed with the use of CasaXPS software version 2.3.15 (Casa Software LTD., Teignmouth, UK, casaxps.com, accessed on 2 March 2015). After subtraction of the Shirley-type background, curve fitting was performed using a mixed 30% Gaussian–Lorentzian peak shape. The P 2p curves were fitted taking into account the spin-orbit splitting of 0.85 eV [48,49] and the intensity ratio of the 2p1/2:2p3/2 components as 1:2. The composition (in at%) was determined by considering the integrated peak areas of C 1s, N 1s, O 1s and P 2p from the survey spectra and the respective sensitivity factors [50].

2.5. 31P MAS NMR

Nuclear magnetic resonance (NMR) spectra were acquired in the solid state with magic angle spinning (MAS) using a Bruker Avance III HD 400WB spectrometer (Bruker, Billerica, MA, USA) at room temperature. 31P MAS NMR spectra were recorded in a single-pulse sequence with a pulse width of 2 ms, a relaxation time of 5 s, and a spinning frequency of 18 kHz. An 85% H3PO4 aqueous solution was used as an external reference for the 31P MAS NMR chemical shift.

2.6. Acid-Base Properties

Acid-base properties of polyimide-derived carbons were investigated by potentiometric titration [51] performed in a thermostatic vessel at 25 °C using a 672 Titroprocessor combined with 655 Dosimat (Metrohm, Herisau, Switzerland). To prevent contamination with CO2, the flow of pure argon was used throughout the titration. The proton concentration was monitored using an LL pH glass electrode (Metrohm, Herisau, Switzerland). Before experiments, the electrode electromotive force was calibrated to proton concentration by blank titration. Solution equilibria and a correction for possible carbonate and silicate contaminations were calculated using EST software [52]. Proton affinity distributions, F(pKa), were calculated from proton-binding isotherms by solving the adsorption integral equation using the CONTIN method [53,54,55,56].

2.7. Copper Binding

The batch technique was used for the determination of copper adsorption. Weighed amounts of adsorbent (0.1 ± 0.0001 g) were placed into Erlenmeyer flasks. A volume of 20 mL containing 0.1 M NaCl solution as background electrolyte and 0.001 M copper ion solution was added to each flask. Then different amounts of either 0.1 M HCl or 0.1 M NaOH were added to change the solution pH. To attain equilibrium the flasks were shaken for 24 h. After equilibration, the pH was measured with a glass electrode and the metal ion concentration was determined titrimetrically with EDTA. Copper binding is given in dimensionless units, defined as the quantity of adsorbed copper divided by the total amount of copper in the adsorption system.

3. Results and Discussion

3.1. Porous Structure

Nitrogen adsorption-desorption isotherm for parent BM-DVB copolymer belongs to type II of IUPAC classification [57] characteristic to adsorption on nonporous or macroporous adsorbents (Figure 2a). On the contrary, the isotherms for carbons obtained by carbonization of BM-DVB copolymer can be attributed to a combination of type I and IVa of IUPAC classification. A steep rise of nitrogen uptake at very low p/p0 is due to adsorption in narrow micropores with enhanced potential while the gradual increase in nitrogen adsorption at medium to high relative pressures corresponds to monolayer-multilayer adsorption in mesopores followed by capillary condensation accompanied by small hysteresis of type H4. The isotherms are typical of micro-mesoporous carbons.
The pore size distribution in the porous polymer BM-DVB reveals a developed mesoporous structure in the range of pores from 12 to 44 nm, with a maximum at 34 nm and the absence of micropores (Figure 2b). Carbonization of a porous polymer in the presence of phosphoric acid results in a complete restructuring of the porous structure, with well-developed porosity appearing in the range of micropores and small mesopores (0.5–5 nm) and the polymer’s developed mesoporous structure transforming into small rudimentary residues. Carbonization of a porous polymer without phosphoric acid, on the other hand, produces an increase in the size of mesopores and the emergence of a microporous structure. It should be noted that the microporous structure of carbon obtained without phosphoric acid is represented by pores in the range of 0.5–1.2 nm, while carbon obtained in the presence of phosphoric acid has additional pores in the range of 1.2–5 nm.
Carbons produced in the presence of phosphoric acid have a more developed porous structure than carbons formed in the absence of acid (Table 1). Phosphoric acid enhances the formation of a microporous structure during carbonation.

3.2. XPS

XPS is a powerful tool for studying the elemental composition and chemical state of phosphorus in carbon materials. An XPS survey scan revealed that both H3PO4 and the Thermal series of carbons contain C, O, and N (Table 2). The Thermal series has a greater carbon content at all temperatures due to the higher oxygen and phosphorus content in carbons activated with phosphoric acid (H3PO4 series), which decreases the proportion of carbon. Phosphorus is only found in carbons that have been activated with phosphoric acid. The phosphorus content increases to 13.2% when carbonization temperature rises to 800 °C and decreases at higher temperatures. This phenomenon is explained by the acceleration of the formation of phosphorus-carbon compounds when the activation temperature is raised to 800 °C and the breakdown of these compounds at higher temperatures [12]. The thermodynamic study discovered that phosphorus compound volatilization is favorable at temperatures greater than 750 °C [12,58]. Furthermore, the thermal gravimetric analysis showed that mass loss in the 800–900 °C temperature range is proportional to phosphorus content [12,59].
The C 1s peak was deconvoluted into the six components: C-C sp2 bonds at 284.7 eV; C-C sp3 at 285.2 eV; C-O at 286.3 eV; C=O at 287.4 eV; O=C-O- at 288.7 eV and shake-up peak that corresponds to π→π* type transitions at 290.5 eV (Figure 3). The content of sp2-hybridized carbon, which belongs to graphite-like fragments of activated carbon, may be obtained by such deconvolution [60,61,62,63]. Carbonization in the presence of phosphoric acid results in a significant increase in the content of sp2-hybridized carbon as the temperature rises from 400 to 500 °C, as seen in Figure 4a. On the contrary, when the BM-DVB copolymer is carbonized without phosphoric acid, the sp2-hybridized content increases over a larger temperature range—from 500 to 800 °C. This demonstrates that phosphoric acid facilitates the formation of the polyaromatic structure of carbon at lower temperatures.
The changes in concentration of π-electrons were also measured by XPS using the π→π* shake-up signal [64,65]. It is seen that the shake-up signal is consistently higher for phosphoric acid-activated carbons (Figure 4b). However, it should be noted, that the shake-up peaks are superimposed on the broad emission of inelastically scattered electrons, which occurs starting in about the same energy region [64].
Deconvolution of the P 2p envelope revealed only one peak with P 2p 3/2 binding energy of 133.1 ± 0.2 eV (Figure 5a). As the carbonization temperature increases, the binding energy shows some tendency to decrease from 133.4 to 132.8 eV. This peak is relatively narrow (FWHM 1.9 ± 0.1 eV), confirming the existence of only one type of phosphorus species. Analysis of the NIST X-ray Photoelectron Spectroscopy Database [49] shows that the detected range of binding energies is typical for phosphates and pyrophosphates (Figure 6). A similar classification was made for other phosphorus-containing carbons obtained by phosphoric acid activation of polymer and lignocellulosic materials [15,16,66].
However, the surface atomic O/P ratio reaches a value of 2.1 for carbon obtained at 600 °C, which suggests the presence of not only phosphates/pyrophosphates (oxyphosphorus compounds with P-O bonds) but also substituted phosphates such as carbophosphorus (P-C bonds) and azaphosphorus (P-N bonds) compounds (Figure 5b).

3.3. 31P MAS NMR

Figure 7a shows 31P MAS NMR spectra of polyimide-derived carbons obtained with phosphoric acid (H3PO4 series) at different temperatures. A sharp peak at about 0 ppm and a somewhat broad signal at 7–12 ppm are visible in the 31P NMR spectra. With confidence, phosphate structures may be attributed to the sharp peak. The second signal is rather broad and asymmetric, indicating the presence of a mixture of orthophosphates and/or quadruply attached phosphorus in an asymmetric environment. To reveal these components the spectra were deconvoluted into five peaks using a Lorentzian line shape (Figure 7b). The results of deconvolution are presented in Figure 7b. The peak P1 at around −10 ppm (Figure 8a) only shows up as a shoulder in the main peak P2. The peak P1 may be ascribed to polyphosphate end groups belonging mainly to PO4 groups linked by one bridging oxygen atom [16,32,35,67,68,69,70,71]. The content of polyphosphates is rather small but increases to 24–26% for carbons obtained at 800–900 °C (Figure 8b). The peak P2 around 0 ppm is sharp and with confidence may be ascribed to orthophosphate structural units linked to polyaromatic graphene framework [16,32,35,67,68,69,70]. The peak P2 shifts from 0 to −6.0 ppm with increasing carbonization temperature due to the increasing positive shielding from π-electrons of enlarged graphene layers [16,22,32] (Figure 8a). The peaks P3 and P4 could be ascribed to pyrophosphate diesters [72] and metal phosphates [73]. The formation of pyrophosphate diesters that crosslink the fragments of polymer structure at high temperature is reasonable and was proposed as activating mechanism of phosphoric acid [74]. The highest amount of pyrophosphate diesters is produced around 500 °C, however, when carbonization temperature rises above this point, cross-linking becomes less prominent until it nearly completely disappears at 800–1000 °C (Figure 8b). At high temperatures, orthophosphate structural units become the dominant structure of phosphorus compounds. The peak P5 at 25–30 ppm is ascribed to phosphonates [75]. The content of phosphonates is small at all temperatures and amounts to 1–9%. Thus, the 31P MAS NMR investigation revealed the existence of different types of phosphates as well as phosphonates in the structure of polyimide-derived carbon obtained with phosphoric acid at different temperatures (H3PO4 series).

3.4. Acid-Base Properties

All phosphorus-containing surface compounds discovered by XPS and 31P MAS NMR techniques, including phosphates, pyrophosphates, and phosphonates, are acidic, and their presence in the carbon structure imparts an acidic character. Proton-binding isotherms show that the carbon obtained without phosphoric acid is amphoteric, that is, it is capable of both adsorption of protons in an acidic solution and dissociation of protons in an alkaline medium (Figure 9a). The point of zero charge (PZC), where the sorption of protons is zero, for this carbon is 8.6. On the contrary, the proton-binding isotherm for carbon obtained with phosphoric acid is located entirely in the negative region (Figure 9a). The point of zero charge for this carbon has not even been reached, but extrapolation gives a value of 2.3, which is close to the pKa of phosphoric acid.
The shape of the proton-binding isotherm for phosphorus-containing carbon is characteristic of multifunctional cation exchangers containing functional groups of different acid strengths. Proton affinity distributions of acid groups calculated by the CONTIN method show two types of acid surface groups for carbon obtained without phosphoric acid (Figure 9b). They can be classed as enol or lactone groups (0.090 mmol/g, pKa 9.7) and phenolic groups (0.266 mmol/g, pKa 11.7). Proton affinity distribution for carbon obtained with phosphoric acid shows six types of surface groups that may be classed as phosphates (0.799 mmol/g, pKa1 2.97, 0.515 mmol/g, pKa2 6.69), carboxylic (0.226 mmol/g, pKa 5.16), and two types of enol and/or lactone (0.107 mmol/g, pKa 8.21 and 0.494 mmol/g, pKa 9.33) and phenolic groups (1.118 mmol/g, pKa 11.16) (Figure 9b). This result shows radically different surface chemistry of carbon obtained with phosphoric acid compared to carbon prepared without acid.

3.5. Copper Binding

Figure 10 shows the pH dependence of copper binding by polyimide-derived carbons obtained with (H3PO4 series) and without phosphoric acid (Thermal series). Adsorption of copper ions on all studied adsorbents increases with an increase in the pH of the solution. The increase in copper adsorption with increasing pH occurs due to the deprotonation of surface functional groups and the formation of surface complexes with copper ions [76,77,78,79,80]. Carbon obtained without phosphoric acid shows very small adsorption of copper at pH < 5.3 and follows the precipitation curve at higher pHs. This behavior is expected since carbon obtained without phosphoric acid does not have surface groups capable of dissociation at pH less than 5–6.
On the contrary, the adsorption of copper on polyimide-derived carbon obtained with phosphoric acid is significant even at a very low pH (Figure 10). This carbon exhibits noticeably greater copper adsorption than the cation-exchange resin with carboxylic groups KB-4 (an analog of Amberlite IRC 86), which has a very high cation exchange capacity of 10 mmol/g. Adsorption of copper on the carbon is even greater than that on the very acidic cation exchange resin KU-23 containing sulfo groups (analog to Amberlyst-15) with a cation exchange capacity of 4.5 mmol/g. Despite having a lower cation-exchange capacity of 2.5 mmol/g, phosphorus-containing carbon removes more copper than ion-exchange resins. This shows that phosphorus-containing carbon has a higher affinity for copper ions than ion-exchange resins.
It is worth noting that polyimide-derived carbon obtained with phosphoric acid exhibits significant copper uptake at pH values lower than PZC (pH < 2.3), i.e., when the surface of carbon is positively charged, and therefore cation adsorption should be hindered. This phenomenon has been reported previously for the adsorption of Cd(II), Hg(II), and Cr(III) and has been explained as being due to an ion exchange reaction between the delocalized protonated π-electrons of the graphene layer of carbon (-Cπ-H3O+) and the metal cation [81,82,83,84,85]. The high adsorption capacity of polyimide-derived carbon obtained with phosphoric acid in an acidic environment indicates its potential for the extraction of heavy metal ions from acidic solutions, as well as its use as an enterosorbent for detoxification of the body from toxic metals in the acidic environment of the stomach.

4. Conclusions

Carbonization of porous polyimide copolymer results in the formation of carbon adsorbents with a developed porous structure (ABET is up to 891 m2/g). Carbons produced in the presence of phosphoric acid have a more developed porous structure than carbons formed in the absence of acid. Phosphoric acid enhances the formation of a microporous structure during carbonation.
The chemical structure of polyimide-derived carbons obtained with and without phosphoric acid has been investigated by XPS and 31P MAS NMR methods. Deconvolution of the P 2p peak with variable binding energy showed the presence of only phosphates/polyphosphates. However, a low value of the O/P ratio is an indirect indication of the possible presence of phosphonates. 31P MAS NMR study revealed the existence of several kinds of phosphates as well as a minor quantity (1–9%) of phosphonates.
All the structures of phosphorus compounds (phosphates and phosphonates) detected by XPS and 31P MAS NMR methods have acidic properties and therefore impart the carbon surface an acidic character. The presence of phosphorus-containing compounds gives carbon the ability to absorb metal cations. Polyimide-derived carbon obtained with phosphoric acid has a large sorption capacity for copper, which exceeds adsorption by ion-exchange resins with carboxyl or sulfo groups. Despite having a lower cation-exchange capacity, phosphorus-containing carbon removes more copper than ion-exchange resins. This shows that phosphorus-containing carbon has a higher affinity for copper ions than ion-exchange resins. Phosphorus-containing polyimide-derived carbon is a potential adsorbent for the concentration, separation, or removal of harmful metal contaminants from potable water, wastewater, and other aqueous environments due to its high adsorption capacity for metal cations.

Author Contributions

Investigation, O.I.P., M.S. (Magdalena Sobiesiak) and M.S. (Myroslav Sprynskyy); Supervision, A.M.P.; Writing—original draft, A.M.P.; Writing—review & editing, B.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

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Carbon 08 00047 g001 550
Figure 1. The chemical formula of 4,4′-bis(maleimidodiphenyl) methane.
Figure 1. The chemical formula of 4,4′-bis(maleimidodiphenyl) methane.
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Carbon 08 00047 g002 550
Figure 2. Nitrogen adsorption-desorption isotherms: (a) and pore size distributions; and (b) for parent BM-DVB copolymer and carbons obtained by carbonization at 600 °C of polyimide copolymer in the presence of phosphoric acid (H3PO4) and without acid (Thermal).
Figure 2. Nitrogen adsorption-desorption isotherms: (a) and pore size distributions; and (b) for parent BM-DVB copolymer and carbons obtained by carbonization at 600 °C of polyimide copolymer in the presence of phosphoric acid (H3PO4) and without acid (Thermal).
Carbon 08 00047 g002
Carbon 08 00047 g003 550
Figure 3. High-resolution X-ray photoelectron spectrum of C 1s peak of polyimide-derived carbon obtained with phosphoric acid at 800 °C.
Figure 3. High-resolution X-ray photoelectron spectrum of C 1s peak of polyimide-derived carbon obtained with phosphoric acid at 800 °C.
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Carbon 08 00047 g004 550
Figure 4. Temperature evolution of sp2-hybridized carbon content: (a) and π→π* shake-up signal (b) of polyimide-derived carbons obtained with (H3PO4-series) and without (Thermal-series) phosphoric acid at different temperatures.
Figure 4. Temperature evolution of sp2-hybridized carbon content: (a) and π→π* shake-up signal (b) of polyimide-derived carbons obtained with (H3PO4-series) and without (Thermal-series) phosphoric acid at different temperatures.
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Carbon 08 00047 g005 550
Figure 5. High-resolution X-ray photoelectron spectrum of P 2p peak of polyimide-derived carbon obtained with phosphoric acid at 800 °C (a) and temperature evolution of phosphorus content and atomic O/P ratio (b).
Figure 5. High-resolution X-ray photoelectron spectrum of P 2p peak of polyimide-derived carbon obtained with phosphoric acid at 800 °C (a) and temperature evolution of phosphorus content and atomic O/P ratio (b).
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Carbon 08 00047 g006 550
Figure 6. P 2p 3/2 binding energies of different types of phosphorus-containing compounds. Data from NIST X-ray Photoelectron Spectroscopy Database [49].
Figure 6. P 2p 3/2 binding energies of different types of phosphorus-containing compounds. Data from NIST X-ray Photoelectron Spectroscopy Database [49].
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Figure 7. 31P MAS NMR spectra of polyimide-derived carbons obtained with phosphoric acid (H3PO4-series) at different temperatures (a) and deconvolution of 31P MAS NMR spectrum of polyimide-derived carbon obtained with phosphoric acid at 600 °C (b).
Figure 7. 31P MAS NMR spectra of polyimide-derived carbons obtained with phosphoric acid (H3PO4-series) at different temperatures (a) and deconvolution of 31P MAS NMR spectrum of polyimide-derived carbon obtained with phosphoric acid at 600 °C (b).
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Carbon 08 00047 g008 550
Figure 8. Chemical shift (a) and relative area (b) of deconvoluted components of 31P MAS NMR spectra of polyimide-derived carbons obtained with phosphoric acid (H3PO4-series) at different temperatures.
Figure 8. Chemical shift (a) and relative area (b) of deconvoluted components of 31P MAS NMR spectra of polyimide-derived carbons obtained with phosphoric acid (H3PO4-series) at different temperatures.
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Figure 9. Proton-binding isotherms (a) and proton affinity distributions (b) for polyimide-derived carbons obtained with (H3PO4 series) and without (Thermal series) phosphoric acid at 800 °C.
Figure 9. Proton-binding isotherms (a) and proton affinity distributions (b) for polyimide-derived carbons obtained with (H3PO4 series) and without (Thermal series) phosphoric acid at 800 °C.
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Figure 10. Copper binding by polyimide-derived carbons obtained with (H3PO4-series) and without (Thermal-series) phosphoric acid at 800 °C. Copper binding by ion-exchange resins with carboxyl (KB-4) and sulfo groups (KU-23) is provided for comparison.
Figure 10. Copper binding by polyimide-derived carbons obtained with (H3PO4-series) and without (Thermal-series) phosphoric acid at 800 °C. Copper binding by ion-exchange resins with carboxyl (KB-4) and sulfo groups (KU-23) is provided for comparison.
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Table
Table 1. Porous structure parameters for parent porous copolymer BM-DVB and polyimide-derived carbons obtained with (H3PO4-series) and without (Thermal-series) phosphoric acid at different temperatures.
Table 1. Porous structure parameters for parent porous copolymer BM-DVB and polyimide-derived carbons obtained with (H3PO4-series) and without (Thermal-series) phosphoric acid at different temperatures.
Temperature °CABET m2/gVtot cm3/gVmi cm3/gVme cm3/g
BM-DVB
55.90.3380.006 (2%)0.332 (98%)
H3PO4 series
40011.50.0260.002 (9%)0.023 (91%)
500520.20.2630.197 (75%)0.066 (25%)
600891.10.4220.324 (77%)0.098 (23%)
700676.30.3360.259 (77%)0.078 (23%)
800599.40.3160.228 (72%)0.088 (28%)
900659.70.3370.255 (76%)0.082 (24%)
1000601.90.3200.231 (72%)0.090 (28%)
Thermal series
40036.50.2280.004 (2%)0.223 (98%)
50037.50.1820.006 (3%)0.176 (97%)
600491.30.3490.174 (50%)0.175 (50%)
700522.00.3280.194 (59%)0.134 (41%)
800356.50.1990.129 (65%)0.070 (35%)
900223.90.1710.080 (47%)0.090 (53)
100020.30.0730.002 (2%)0.071 (98)
Table
Table 2. Chemical composition (in mass%) of polyimide-derived carbons.
Table 2. Chemical composition (in mass%) of polyimide-derived carbons.
Temperature °CH3PO4 SeriesThermal Series
CONPCON
40081.212.62.62.279.7155.3
50074.215.22.36.684.210.45.4
60074.512.31.611.691.14.34.6
70068.9153.712.493.22.93.9
80066.117.13.613.293.33.43.3
90068.617.33.410.694.432.6
100075.814.11.78.3923.92.6
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Puziy, A.M.; Poddubnaya, O.I.; Gawdzik, B.; Sobiesiak, M.; Sprynskyy, M. Structural Evolution of Polyimide-Derived Carbon during Phosphoric Acid Activation. C 2022, 8, 47. https://doi.org/10.3390/c8030047

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Puziy AM, Poddubnaya OI, Gawdzik B, Sobiesiak M, Sprynskyy M. Structural Evolution of Polyimide-Derived Carbon during Phosphoric Acid Activation. C. 2022; 8(3):47. https://doi.org/10.3390/c8030047

Chicago/Turabian Style

Puziy, Alexander M., Olga I. Poddubnaya, Barbara Gawdzik, Magdalena Sobiesiak, and Myroslav Sprynskyy. 2022. "Structural Evolution of Polyimide-Derived Carbon during Phosphoric Acid Activation" C 8, no. 3: 47. https://doi.org/10.3390/c8030047

APA Style

Puziy, A. M., Poddubnaya, O. I., Gawdzik, B., Sobiesiak, M., & Sprynskyy, M. (2022). Structural Evolution of Polyimide-Derived Carbon during Phosphoric Acid Activation. C, 8(3), 47. https://doi.org/10.3390/c8030047

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