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Article

Catalytic Hydrodechlorination of Chlorophenols in a Continuous Flow Pd/CNT-Ni Foam Micro Reactor Using Formic Acid as a Hydrogen Source

by
Jun Xiong
*,† and
Ying Ma
†
School of Pharmacy, Zunyi Medical University, Guizhou 510640, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Catalysts 2019, 9(1), 77; https://doi.org/10.3390/catal9010077
Submission received: 16 December 2018 / Revised: 31 December 2018 / Accepted: 8 January 2019 / Published: 12 January 2019
(This article belongs to the Special Issue Catalytic Methods in Flow Chemistry)
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Abstract

:
Catalytic hydrodechlorination (HDC) has been considered as a promising method for the treatment of wastewater containing chlorinated organic pollutants. A continuous flow Pd/carbon nanotube (CNT)-Ni foam micro reactor system was first developed for the rapid and highly efficient HDC with formic acid (FA) as a hydrogen source. This micro reactor system, exhibiting a higher catalytic activity of HDC than the conventional packed bed reactor, reduced the residence time and formic acid consumption significantly. The desired outcomes (dichlorination >99.9%, 4-chlorophenol outlet concentration <0.1 mg/L) can be obtained under a very low FA/substrate molar ratio (5:1) and short reaction cycle (3 min). Field emission scanning electron microcopy (FESEM) and deactivation experiment results indicated that the accumulation of phenol (the main product during the HDC of chlorophenols) on the Pd catalyst surface can be the main factor for the long-term deactivation of the Pd/CNT-Ni foam micro reactor. The catalytic activity deactivation of the micro reactor could be almost completely regenerated by the efficient removal of the absorbed phenol from the Pd catalyst surface.

Graphical Abstract

1. Introduction

Chlorophenols (CPs), existing widely in polluted groundwater and the wastewater effluents of industry [1,2], have been listed as priority pollutants in many countries because of their high toxicity, adverse environmental impacts and poor biodegradability [3,4,5]. For the safe disposal of these highly toxic chlorinated organic pollutants, many detoxification techniques such as biodegradation [6], photochemical degradation [5], advanced oxidation [7,8] and catalytic hydrodechlorination [9,10] have been proposed. Among the available water treatment techniques mentioned above, hydrodechlorination (HDC) presents the advantages of greater flexibility, low energy consumption and relatively safe by-products, showing promising prospects in the treatment of wastewater containing chlorinated organic pollutants [11,12,13].
Molecular hydrogen (H2) is the most widely employed hydrogen source for HDC [10,14,15,16,17,18]. However, the low H2 utilization efficiency caused by its very low solubility in water (0.84 mM, at 288 K and PH2 = 100 kPa) [19,20], and the low process safety associated with hydrogen gas usage [21,22], may lead to some adverse influences during the treatment of wastewater on a large scale through HDC. To overcome these drawbacks, other potential hydrogen sources, including isopropanol, hydrazine, formic acid and formate, have been reported [19,20,23,24]. Formic acid, with high solubility in water, has been proven to be a promising alternative hydrogen source of HDC [14,20].
The HDC of chlorinated organic compounds are generally performed in a conventional batch reactor with a powder Pd catalyst [11,25,26,27,28]. A high formic acid (FA) consumption (FA/substrate molar ratio ≥35:1) and relatively long reaction time (tens of minutes or several hours) is required for a high dechlorination of the substrate during HDC, as FA is utilized to provide hydrogen [14,19,20,23]. Furthermore, the inherent difficulty of scale-up is still a challenge during the industrial application of a batch reactor system [29,30]. The application of a small-scale continuous flow reactor (micro reactor) system may offer some advantages, especially for heterogeneous catalytic reactions such as HDC, over a conventional batch reactor system [29]. The micro reactor, with short diffusion paths and large interfacial areas, can provide efficient mixing and fast mass transfer during HDC, contributing to the achievement of desired outcomes (e.g., high dechlorination, low FA consumption and short reaction cycle) [30,31,32]. Scaling up a continuous reactor system is also generally easier than scaling up a batch reactor system [30,33,34]. Thus, it is interesting to develop a new micro reactor system for HDC in continuous flow.
A carbon nanotube (CNT)-Ni foam-supported Pd catalyst has been found to be an excellent catalyst candidate for HDC [35]. Notably, this monolithic Pd/CNT-Ni foam composite catalyst can also be utilized as a micro reactor, due to its highly porous channel with a micrometer size and well-dispersed active Pd catalyst on the surface of the micro channel. Herein, we report the usage of a micro reactor system for conducting HDC in continuous flow for the first time. Our aim is to develop a new micro reactor system possessing a high catalytic HDC performance. The Pd/CNT-Ni foam micro reactor system was configured and its HDC of CPs was evaluated in detail by using the safe and efficient formic acid as a hydrogen source. Finally, the long-term deactivation and regeneration of the Pd/CNT-Ni foam micro reactor were investigated.

2. Results and Discussion

2.1. Catalyst Characterization

Figure 1 presents Field emission scanning electron microcopy (FESEM) results of the Pd/CNT-Ni foam micro reactor. A highly porous Ni foam skeleton with irregular micro channels of about 150–500 µm in size (Figure 1a) was found in this monolithic micro reactor. Uniformly dispersed Pd nanoparticles were observed on the CNT surface of the fresh Pd/CNT-Ni foam micro reactor, and their amount increased significantly with the Pd loading (Figure 1b,c). The micro reactors were used for 76 h and deactivated with a high-concentration phenol solution, following which similar organic layers were observed on the Pd catalyst surface (Figure 1d,e). After regeneration treatment, the organic layer covered on the Pd catalyst surface disappeared (Figure 1f), indicating an efficient removal of the absorbed organic layer from the catalyst surface during regeneration.
The fresh and used Pd/CNT-Ni foam micro reactors were also investigated by TEM/HRTEM. Figure 2a shows that the Pd particles were well dispersed in a fresh Pd/CNT-Ni foam micro reactor, which is consistent with the FESEM observation. The average particle size was about 2.68 nm (Figure 2c). The nanoparticle composition was confirmed to be metal Pd by the HRTEM results and the corresponding fast Fourier transform (FFT). The lattice plane with the interplanar distance of 2.26 Å and its corresponding FFT pattern, assigned to the (111) plane of the face-centered cubic (fcc) Pd, are presented in Figure 2e [36,37]. The Pd particle characteristics including dispersion, size distribution and composition in the used micro reactor (Figure 2b,d,f) are almost the same as those presented in the fresh micro reactor, revealing the excellent stability of Pd particles during HDC.

2.2. HDC of 4-CP in Continuous Flow Micro Reactor and Packed Bed Reactor

For a comparison of the catalytic performance between the micro reactor and packed bed reactor, the HDC evaluations were controlled at analogous reaction conditions, such as the same reactor volume (about 4.8 mL), residence time and FA/substrate molar ratio. As shown in Figure 3, a significant increase in dechlorination and decrease in 4-CP outlet concentration was observed when switching from the packed bed reactor to the micro reactor. Desired outcomes (dichlorination >99.9%, 4-CP outlet concentration <0.1 mg/L) of HDC was obtained in the micro reactor. With the reduction of the FA/substrate molar ratio from 5:1 to 2:1, the enhancement of catalytic activity in the micro reactor would be increased.
For HDC with the alternative hydrogen source of FA (a typical liquid–solid heterogeneous catalytic process), the reaction rate depends on the concentration of the reactants (4-CP and FA) available on the catalyst surface sites, which means that the observed catalytic activity is influenced by both the surface hydrodechlorination reaction rate and the reactants’ mass transport rate from the liquid phase to the catalyst surface [34,38]. In this work, the reaction scale is reasonable enough to be the main difference between the micro reactor and packed bed reactor, because these two heterogeneous catalytic reactors possess the same catalyst characteristics, including active Pd loading (0.5 wt.%) and Pd particle size (about 2.68 nm). Generally, the reduction of the reaction channel to a micro size is beneficial for enhancing the mass transport rate of reactants significantly [29,31,32,39]. Therefore, a higher HDC activity was exhibited by the micro reactor. In HDC, by using FA as a hydrogen source, a higher FA concentration on catalyst surface sites is necessary to generate a sufficient Pd-H reactive species, due to the incomplete FA decomposition during reaction [14,23]. A micro reactor with a very short diffusion distance can undoubtedly improve the refill of FA on the catalyst surface, especially under a low FA/substrate molar ratio. That is why the more obvious advantage of the micro reactor was observed under a lower FA/substrate molar ratio.

2.3. HDC of 4-CP in Micro Reactor with Different Pd Contents

Figure 4 shows 4-CP dechlorination in a continuous flow Pd/CNT-Ni foam micro reactor with different Pd contents. For the micro reactor without Pd, a very low dechlorination (<5%) of 4-CP was found. A significant decrease of 4-CP dechlorination from 80.2% to 47.8% during the first 6 h was presented by the micro reactor with 0.1 wt.% Pd. The catalytic activity and stability were obviously enhanced by the increase of Pd loading from 0.1 to 0.5 wt.%. A very highly efficient and stable HDC of 4-CP was exhibited by the micro reactor with 0.5 wt.% Pd. No significant changes of 4-CP dechlorination and catalytic stability were observed with the further increase of Pd content in the micro reactor from 0.5 to 2 wt.%.
In the HDC mechanism (Scheme 1) [38], the CPs (4-CP) were adsorbed on the surface sites of the Pd catalyst and consumed by the surface hydrodechlorination reaction, involving the adsorbed atomic hydrogen and adsorbed CPs. The accumulation of 4-CP on the catalyst surface may occur, as the surface reaction rate is very low. For the micro reactors with a lower Pd loading (less than 0.2 wt.%), the surface reaction rate is expected to be lower, due to the limited availability of active Pd sites (Figure 1b). Jadbabaei et al. [38] reported the obvious catalytic deactivation caused by the 4-CP accumulation on the surface of a catalyst with a low Pd loading (<0.44 wt.%) during the HDC of 4-CP. This phenomenon was also observed during our study. For the micro reactor with 0.1 wt.% Pd, the 4-CP dechlorination decreased rapidly from 80.2% to 47.8%. The catalyst active surface sites in the low Pd loading micro reactor were gradually covered by the accumulating 4-CP during the reaction, resulting in the reduction of the HDC catalytic activity. Thus, the micro reactors with lower Pd loadings (0.1 and 0.2 wt.%) present lower catalytic activity and stability. As the Pd loading in the micro reactor increased, the surface reaction could be accelerated by the increase in active Pd sites (Figure 1b,c) [40,41]. Additionally, the accumulation of 4-CP on the catalyst surface was alleviated or even eliminated. Therefore, high catalytic activity (dechlorination >99.9%) and stability was exhibited by the micro reactor with a relatively high Pd loading (≥0.5 wt.%).

2.4. HDC of 4-CP in Micro Reactor under Different FA/Substrate Molar Ratios

The FA decomposition rate is considered to be slower than the hydrodechlorination rate during HDC, although it can be stimulated by hydrodechlorination simultaneously [14,20]. A high FA/substrate molar ratio is required to provide sufficient active adsorbed atomic hydrogen for a highly efficient HDC process. The influence of the FA/substrate molar ratio on the dechlorination of 4-CP during HDC in continuous flow Pd/CNT-Ni foam micro reactor was evaluated. As shown in Figure 5, the catalytic activity and stability were enhanced significantly with the increase of the FA/substrate molar ratio from 1:1 to 5:1. The lower activity and stability under low FA/substrate molar ratios (1:1 and 2:1) may also be attributed to the low 4-CP consumption rate on the catalyst surface caused by the insufficiently active adsorbed atomic hydrogen under these conditions [19,38]. Notably, the FA/substrate molar ratio required for the almost complete dechlorination of 4-CP during HDC in our study was far less than that reported in other works [20,23].

2.5. The Longevity, Deactivation and Regeneration of Pd/CNT-Ni Foam Micro Reactor

An HDC durability test was conducted for the evaluation of long-term catalytic stability in a continuous flow Pd/CNT-Ni foam micro reactor. Figure 6a shows the 4-CP dechlorination as a function of reaction time. The 4-CP dechlorination maintains a very high and stable value (≥99.9%) during the initial 30 h. However, a gradual loss of catalytic activity with reaction time was observed after 30 h. Only 60.9% dechlorination of 4-CP was found at the final 76th hour. The long-term deactivation of HDC could occur in a continuous flow Pd/CNT-Ni foam micro reactor.
HCl poisoning, which may induce severe Pd leaching and the alteration of Pd particles through corrosive action, has been widely reported as an important factor of Pd catalyst deactivation during HDC [12,38,42,43]. In our study, the continuous flow operation in the micro reactor achieved a more effective removal of HCl from the Pd catalyst surface, limiting the influences of HCl by-products during HDC [44]. Additionally, Pd particles with excellent stability, which may result from the strong interaction between the transition metal (Pd) atoms and sp2-hybridized carbon atoms [12,45], is expected to be resistant to HCl poisoning during the very short residence time (3 min). These inferences were supported by the Pd leaching measurement and TEM/HRTEM analysis. As illustrated in Figure 6b, Pd leaching in the effluents of the micro reactor was very low (<0.05 ppm) and almost undetectable (<0.01 ppm) after the 10th hour. The dispersion, distribution and composition of Pd particles were also largely unchanged during 76 hours of reaction time (Figure 2). Therefore, the influence of HCl poisoning on the catalytic stability was not significant during HDC in the Pd/CNT-Ni foam micro reactor.
The fresh and used Pd/CNT-Ni foam micro reactors were further investigated by FESEM. It was found that the Pd catalyst surface in the Pd/CNT-Ni foam micro reactors was covered by an organic layer after 76 h (Figure 1c,d). The used Pd/CNT-Ni foam micro reactor was soaked in ethanol for 4 h to perform an organics partial desorption test. Many phenols (about 37.8 mg/L in solution), the main product for the HDC of 4-CP, were detected. To confirm the role of phenol accumulation on the deactivation of the Pd/CNT-Ni foam micro reactor, a deactivation experiment with a high-concentration phenol solution (1 mol/L) treatment was carried out for 4 h. A similar organic layer to that caused by phenol accumulation was observed on the catalyst surface of the deactivated micro reactor (Figure 1e). According to the HDC performance results shown in Figure 7, serious deactivation of the Pd/CNT-Ni foam micro reactor was observed. The 4-CP dechlorination decreased remarkably from almost 100% to a very low level, less than 15%. Serious deactivation of HDC induced by phenol accumulation on the Pd catalyst surface was also observed in the work of Jadbabaei et. al. [38].
Lastly, a deactivated Pd/CNT-Ni foam micro reactor was regenerated for 3 h in an argon atmosphere (20 mL/min flow rate) at 250 °C. An almost complete recovery of the HDC catalytic activity was presented by the regenerated micro reactor (Figure 7), due to the efficient removal of the absorbed phenol layer from the Pd catalyst surface during the regeneration process (Figure 1f). This result demonstrated that the Pd/CNT-Ni foam micro reactor system can be regenerated efficiently through a simple heating process, facilitating its practical application significantly.

3. Materials and Methods

3.1. Preparation of Pd/CNT-Ni Foam Micro Reactor (Pd/CNT-Ni Foam Composite Catalyst)

A detailed preparation of the Pd/CNT-Ni foam micro reactor has been reported in the literature [35]. The active Pd was introduced into the micro channel of a monolithic CNT-Ni foam composite through the wetness incipient impregnation method. The pretreated CNT-Ni foam composite (about 15 wt.% CNTs) was impregnated with an acetone solution, then calcined at 300 °C for 2 h. Finally, the samples were reduced with 20 mL/min hydrogen flow at 300 °C for 2 h.

3.2. Catalytic Performance Evaluation

The HDC performance evaluations in micro reactors were carried out in a continuous flow Pd/CNT-Ni foam micro reactor system (Figure 8a) at room temperature and atmospheric pressure. Seven pieces of 65 × 6 × 1.8 mm (L × W × H) Pd/CNT-Ni foam micro reactor (about 1.5 g) were embedded into the stainless steel reaction chamber (Figure 8b) to assemble the reactor system with two fixed stainless steel plates. The 4-CP (1 mmol/L) and FA aqueous solution with an appropriate flow rate was made to flow into a micro reactor through a micro pump. The effluent liquid products of the reactor were collected for further analysis.
We also evaluated the HDC performance in a continuous flow packed bed reactor with a Pd/CNT-Ni foam composite catalyst. Small pieces of Pd/CNT-Ni foam composite catalysts (3 × 3 × 1.8 mm) were packed into a 100-mm length of quartz tubing (8 mm I.D.) to assemble the packed bed reactor. The reagents aqueous solution was then pumped into the reactor, and the effluent liquid products of the reactor were collected for further analysis.
The effluent liquid samples were analyzed by high-performance liquid chromatography (HPLC) with a Zorbax XDB-C18 column (Agilent, USA) [1,12,35]. Inductively coupled plasma mass-spectrometry (ICP-MS) was employed to measure the Pd contents in the effluents.

3.3. Catalyst Characterization

A JSM-4800F electron microscope (JEOL Ltd., Tokyo, Japan) was employed for the field emission scanning electron microcopy (FESEM) analysis. To carry out transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM) on A JEOL-2100F electron microscope (JEOL Ltd., Tokyo, Japan), the powder Pd/CNTs sample was prepared by separating it from the Ni foam skeleton through hydrochloric acid (0.1 M) immersion and ultrasonic treatment. The tests of Pd concentration in the effluents were conducted through Agilent 7500a (Agilent, USA) inductively coupled plasma mass-spectrometry.

4. Conclusions

The HDC of CPs using FA as a hydrogen source was investigated for the first time in a continuous flow micro reactor. A continuous flow Pd/CNT-Ni foam micro reactor system was developed for the rapid and highly efficient HDC of CPs. This micro reactor system, providing a micro size reaction channel (100–500 µm) and well-dispersed Pd nanoparticles (2.68 nm), exhibited a higher catalytic activity of HDC compared with the conventional packed bed reactor.
The influences of the Pd content and FA/substrate molar ratio on HDC performance in a continuous flow micro reactor were discussed. A very low FA/substrate molar ratio (5:1) and short reaction time (3 min) were required to obtain the desired outcomes (dichlorination >99.9%, 4-CP outlet concentration <0.1 mg/L) for a micro reactor with 0.5 wt.% Pd loading. Moreover, the long-term deactivation of HDC, which can be mainly attributed to the phenol accumulation on the Pd catalyst surface, was observed. The catalytic activity deactivation of this micro reactor system can be almost completely recovered by the efficient removal of the absorbed phenol layer from the Pd catalyst surface, making it a promising candidate for the HDC of wastewater containing highly toxic chlorinated organic pollutants and other Pd-catalyzed hydrogenation reactions.
This work shows that the usage of a micro reactor system is practicable and highly efficient for HDC in continuous flow. Future plans involve the development of a new Pd-based micro reactor system with designable structures and unique physical and chemical properties, which could remove target contaminants and enable the in situ regeneration of active components simultaneously.

Author Contributions

This study was conducted through contributions of all authors. J.X. designed the study, performed the experiments, and wrote the manuscript. Y.M. was involved in performing the experiments.

Funding

This work was supported by the Natural Science Foundation of China (grant number 21463030) and the Guizhou Province Technology Department of China (grant number QKHLHZ-2014-7550).

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Field emission scanning electron microcopy (FESEM) images of 0.5 wt.% fresh (a,c), 0.2 wt.% fresh (b), 0.5 wt.% used (d), 0.5 wt.% deactivated with phenol (e) and 0.5 wt.% regenerated (f) Pd/carbon nanotube (CNT)-Ni foam micro reactors. The inset in (a) is the photograph of the Pd/CNT-Ni foam micro reactor.
Figure 1. Field emission scanning electron microcopy (FESEM) images of 0.5 wt.% fresh (a,c), 0.2 wt.% fresh (b), 0.5 wt.% used (d), 0.5 wt.% deactivated with phenol (e) and 0.5 wt.% regenerated (f) Pd/carbon nanotube (CNT)-Ni foam micro reactors. The inset in (a) is the photograph of the Pd/CNT-Ni foam micro reactor.
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Figure 2. TEM (a,b) images and HRTEM (e,f) images of the fresh and used Pd/CNT-Ni foam micro reactors, respectively. (c,d) The corresponding particle size distribution of (a,b). The insets in (e,f) are the fast Fourier transform (FFT) patterns corresponding to the labeled regions.
Figure 2. TEM (a,b) images and HRTEM (e,f) images of the fresh and used Pd/CNT-Ni foam micro reactors, respectively. (c,d) The corresponding particle size distribution of (a,b). The insets in (e,f) are the fast Fourier transform (FFT) patterns corresponding to the labeled regions.
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Figure 3. Hydrodechlorination (HDC) performance under 2:1 formic acid (FA)/substrate molar ratio (a) and 5:1 FA/substrate molar ratio (b) in different continuous flow reactors. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), 4-chlorophenol concentration (1 mmol/L).
Figure 3. Hydrodechlorination (HDC) performance under 2:1 formic acid (FA)/substrate molar ratio (a) and 5:1 FA/substrate molar ratio (b) in different continuous flow reactors. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), 4-chlorophenol concentration (1 mmol/L).
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Figure 4. Dechlorination of 4-CP during an HDC reaction in a Pd/CNT-Ni foam micro reactor with different Pd loadings. Reaction conditions: residence time (3 min), FA/substrate molar ratio (5:1), 4-chlorophenol concentration (1 mmol/L).
Figure 4. Dechlorination of 4-CP during an HDC reaction in a Pd/CNT-Ni foam micro reactor with different Pd loadings. Reaction conditions: residence time (3 min), FA/substrate molar ratio (5:1), 4-chlorophenol concentration (1 mmol/L).
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Scheme 1. Mechanism of HDC on the Pd catalyst surface.
Scheme 1. Mechanism of HDC on the Pd catalyst surface.
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Figure 5. Dechlorination of 4-CP during HDC reaction in a Pd/CNT-Ni foam micro reactor under different FA/substrate molar ratios. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), 4-chlorophenol concentration (1 mmol/L).
Figure 5. Dechlorination of 4-CP during HDC reaction in a Pd/CNT-Ni foam micro reactor under different FA/substrate molar ratios. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), 4-chlorophenol concentration (1 mmol/L).
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Figure 6. Dechlorination of 4-CP (a) and Pd outlet concentration (b) as a function of reaction time during HDC reaction in a Pd/CNT-Ni foam micro reactor. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), FA/substrate molar ratio (5:1), 4-chlorophenol concentration (1 mmol/L).
Figure 6. Dechlorination of 4-CP (a) and Pd outlet concentration (b) as a function of reaction time during HDC reaction in a Pd/CNT-Ni foam micro reactor. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), FA/substrate molar ratio (5:1), 4-chlorophenol concentration (1 mmol/L).
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Figure 7. Dechlorination of 4-CP during HDC reaction in fresh, used and deactivated Pd/CNT-Ni foam micro reactors. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), FA/substrate molar ratio (5:1), 4-chlorophenol concentration (1 mmol/L).
Figure 7. Dechlorination of 4-CP during HDC reaction in fresh, used and deactivated Pd/CNT-Ni foam micro reactors. Reaction conditions: residence time (3 min), Pd loading (0.5 wt.%), FA/substrate molar ratio (5:1), 4-chlorophenol concentration (1 mmol/L).
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Figure 8. Sketched configuration of the continuous flow Pd/CNT-Ni foam micro reactor system (a) and the reaction chamber embedded with a Pd/CNT-Ni foam micro reactor (b).
Figure 8. Sketched configuration of the continuous flow Pd/CNT-Ni foam micro reactor system (a) and the reaction chamber embedded with a Pd/CNT-Ni foam micro reactor (b).
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MDPI and ACS Style

Xiong, J.; Ma, Y. Catalytic Hydrodechlorination of Chlorophenols in a Continuous Flow Pd/CNT-Ni Foam Micro Reactor Using Formic Acid as a Hydrogen Source. Catalysts 2019, 9, 77. https://doi.org/10.3390/catal9010077

AMA Style

Xiong J, Ma Y. Catalytic Hydrodechlorination of Chlorophenols in a Continuous Flow Pd/CNT-Ni Foam Micro Reactor Using Formic Acid as a Hydrogen Source. Catalysts. 2019; 9(1):77. https://doi.org/10.3390/catal9010077

Chicago/Turabian Style

Xiong, Jun, and Ying Ma. 2019. "Catalytic Hydrodechlorination of Chlorophenols in a Continuous Flow Pd/CNT-Ni Foam Micro Reactor Using Formic Acid as a Hydrogen Source" Catalysts 9, no. 1: 77. https://doi.org/10.3390/catal9010077

APA Style

Xiong, J., & Ma, Y. (2019). Catalytic Hydrodechlorination of Chlorophenols in a Continuous Flow Pd/CNT-Ni Foam Micro Reactor Using Formic Acid as a Hydrogen Source. Catalysts, 9(1), 77. https://doi.org/10.3390/catal9010077

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