Abstract
Custom design of JMP software was used to optimize the iodine number of coal-based electrode materials. Taking the additive ratio (A), heating rate (B) and final pyrolysis temperature (C) into account and the significance sequence was C>B>A. Set the additive ratio as 0.2, the heating rate as 5°C/min and the final temperature as 900°C, the iodine number was improved to 403.14 mg·g-1, and the compressive strength was 2.01 MPa. Surface morphology of the coal-based electrode materials were characterized by scanning electron microscopy (SEM). The functional group species were explored by Fourier infrared spectrophotometer (FTIR). Then applied the voltage of 4 V, coal-based adsorption materials were set as cathodes and anodes in a 3-dimensional electrode system with the commercial activated carbon as a particle electrode. After 5 h treatment for cyanide wastewater, the removal rate of most ions was achieved to 72% or more. It was the collaborative effect in the combined action of electro-adsorption and electrodeposition.
1 Introduction
Due to the energy shortage and environmental pollution, renewable energy systems are suggested to play an increasing role in the industry and caused global concerns [1], especially the development of sustainable energy [2]. Carbon materials are widely explored as electrode materials because of their excellent electrical conductivity and outstanding electrochemical stability [3]. There are many advances in the synthesis of carbon electrode materials such as carbon nanofibers [4], carbon xerogels [5], carbon spheres [6], carbon nanosheets, carbon-metal oxide composites [7] and the activated carbon (AC) is the typical carbon electrode materials. The electrosorption of ions in aqueous solution by using AC as the electrode was studied in many works [8, 9, 10, 11]. The coal, the petroleum coke, the wood, and the fruit shells can be the raw materials of carbon electrode materials [12]. Numerous researches [13, 14, 15, 16] focused on the pyrolysis process of low-rank coal and oil shale, biomass, waste polymer plastics, coal liquefaction residue, and other organic materials. Due to this, it can be found that the features of AC give a high porous structure as well as an excellent conductivity. Combining the two properties, it can be prepared an excellent electrode for further applications, such as wastewater treatment. In order to
discover the better electrosorption materials, using low-rank coal and coal liquefaction residue as raw materials in here to make a kind of coal-based electrode materials to treat the cyanide wastewater by electrosorption. However, how to obtain a better material becomes a challenge, because it depends on the ratio of materials, heating rate and final pyrolysis temperature. There are no available data reported in the literatures. Considering the experimental cost and efficacy, an effective experimental design is required. Therefore, the custom design of JMP software was adopted in this study. The software is not only to give a statistical analysis but also it can give a quadratic regression. Some powerful statistical methods were designed using JMP software to detect factors contributing to differences in many experiment processes. JMP software was widely used in experimental design in many disciplines such as metallurgy, medicine, management and materials science [17, 18, 19, 20]. Once the materials were prepared at various conditions; characterization was needed. Highly positive correlations with methylene blue and iodine number were observed for AC adsorption capacity [21], in here, Iodine number was acted as an indicator representing the performance of coal-based adsorption materials.
2 Experimental methods
2.1 Materials
The low-rank coal from Sunjiacha (SJC) and the coal direct liquefaction residue (DCLR) were used as raw materials and additives respectively in this study. After de-ashing treatment of the DCLR, they were prepared by crushing, screening and drying at 110°C for 24 h in a vacuum drying oven. The quality percent of sample with particle sizes of less than 80 mesh was above 90%, two powder were mixed with set ratio and stirred with 500 rpm for 2 h. The proximate and ultimate analysis results of SJC and DCLR on an air-dry basis are presented in Table 1 and the ionic components of cyanide wastewater are shown in Table 2.
Proximate and ultimate analysis of SJC and DCLR.
| Proximate and Ultimate analysis/% | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Raw material | M ad | Aad | V ad | * FCad | Cad | * Oad | Had | Nad | St,ad |
| SJC | 4.71 | 5.94 | 34.30 | 55.05 | 73.07 | 4.94 | 4.34 | 0.96 | 0.42 |
| DCLR | 1.15 | 10.42 | 32.24 | 56.19 | 78.59 | 3.26 | 4.22 | 0.99 | 1.26 |
Ionic components of cyanide wastewater (mg/L).
| ion | CNT | CN– | Cu | Zn | SCN– |
|---|---|---|---|---|---|
| Cyanide wastewater | 1728.60 | 367.20 | 546.10 | 456.20 | 260.10 |
The characteristics of high volatile content and low sulfur as well as ash content of SJC are remarkable. The volatile content of DCLR reached at 32.24%, which was slightly lower than that of SJC. DCLR has a higher ash content of 10.42%. The chemical reaction of calcium, magnesium, aluminum, iron and other oxides in ash can affect the pore structure of the coal-based electrode material. Hydrogen content of two is more than 4.0%, and the distribution of hydrogen is directly related to the composition of pyrolysis gas. The porosity and pore size of coal-based electrode material were affected by the content and release rates of pyrolysis gas.
2.2 Furnace equipment
The mixed powder was formed to a coin like tablet with the size of Φ30 mm × 2 mm under a pressure of 8 MPa by FYD-40-A powder press machine, and the coal-based materials were allowed to air dry at room temperature for 24 h. Then the coal-based materials after pyrolysis process were treated with nitric acid (the wt% of coal-based materials and HNO3 was 1:3) for 8 h and whereafter washed to neutrality and dried in oven at 80°C for 12 h to obtain the coal-based electrode materials. The Schematic diagram of the experimental is shown in Figure 1. Gas was dried before collected in a gas bag after air cooling plus double water cooling process.

Schematic diagram of the experimental.
1-Vacuum tube-type furnace, 2-Air cooler, 3-First-water cooler, 4-Secondary water cooler, 5-Silica gel dying device, 6-Airbag
2.3 Analysis and characterization
2.3.1 Yield and removal rate
The yields of pyrolysis without activation (ω), pyrolysis with activation (ω′) and the removal rate (φ) of ions were calculated from Eq. 1, 2 and 3.
where m1 is the quality of coal tablet, g; m2 is the quality of coal tablet after pyrolysis process, g; m3 is the quality of pyrolyzed coal electrode material after nitric acid activation, g; C0 is the initial concentration of ions, mg/L; C1 is the concentration of ions in post-adsorption liquid, mg/L.
2.3.2 Characterization
The compressive strength of coal-based electrode was tested by pellet electronic pressure tester LD-YB-2. Bruker VERTEX70 FTIR spectrometer was used to explore the function group of samples. The morphology of coal-based electrode materials was scanned by Carl Zeiss singma300 scanning Electron Microscopy (SEM).
2.4 Experimental design
Additive was used to assist in the formation of coal-based electrode materials, so a single factor experiment was carried out to learn the influence of the additive ratio (A) on the compressive strength (CS) and then determine the range of additive before response surface experiment design. The setting and compressive strength were shown in Table 3.
The CS of coal-based electrode materials with different A (10°C/min, 800°C).
| A | 0.1 | 0.2 | 0.3 | 0.4 | 0.5 |
| CS/MPa | 1.24 | 1.83 | 1.89 | 1.76 | 1.37 |
Higher CS was found at additive interval of 0.2-0.4. The response surface experiment design was carried out using the response surface design platform of JMP which is a data statistics software. Three parameters, including additive ratio, final pyrolysis temperature (B), heating rate (C), were studied and the setting of each parameter was shown in Table 4. In addition, a total of ten runs were listed in Table 5. Iodine number (IN) was also shown in the last column of this table, which will be discussed later.
Parameters and levels for the response surface design.
| Parameter | Unit | –1 | 0 | 1 |
|---|---|---|---|---|
| A | °C | 0.2 | 0.3 | 0.4 |
| B | – | 700 | 800 | 900 |
| C | °C⋅min–1 | 5 | 10 | 15 |
Experimental conditions conducted in this work.
| No. | A | B | C | IN |
|---|---|---|---|---|
| A-1 | 0.2 | 700 | 5 | 278.46 |
| A-2 | 0.2 | 800 | 10 | 308.08 |
| A-3 | 0.2 | 700 | 15 | 259.02 |
| A-4 | 0.2 | 900 | 15 | 345.60 |
| A-5 | 0.3 | 800 | 15 | 287.02 |
| A-6 | 0.3 | 700 | 10 | 247.98 |
| A-7 | 0.3 | 900 | 5 | 376.08 |
| A-8 | 0.4 | 700 | 15 | 262.74 |
| A-9 | 0.4 | 900 | 10 | 321.20 |
| A-10 | 0.4 | 800 | 5 | 320.84 |
3 Results and discussion
3.1 Iodine number
The iodine number of the coal-based electrode material was tested according to the test method for the iodine adsorption value of coal electrode material (GB/T 7702.7-2008). The coal-based electrode material require higher iodine number for better adsorption performance. The IN values obtained were in the range of 262.74-376.08 mg/g, depending on the operating condition listed in Table 5. This indicates that the operating condition have an effect on the IN value. However, the importance of parameter needs to be analysis further.
3.2 Yield of pyrolysis without activation and pyrolysis with activation
The yields of pyrolysis without activation were within the range of 68.8% to 75.9% in Figure 2a. According to the final temperature, the samples can be divided into 3 groups named high temperature group 1, medium temperature group 2 and low temperature group 3 respectively. The rules of higher final pyrolysis temperature caused the lower pyrolysis yield can be seen from these groups. With the higher final temperature, pyrolysis product will undergo secondary pyrolysis, which reduced the yield of pyrolysis solid product. Overall, the influence of temperature is important for the yield of pyrolysis. The pyrolysis yields with activation varied slightly within the range of 63.0% to 69.7% in Figure 2b. They were also divided into 3 groups and owned the same law as pyrolysis yield without activation. Meanwhile, with the increase of the additive ratio, the yield showed an increasing trend in each group. The sample of A-1 with the lowest yield of pyrolysis with activation but not the lowest pyrolysis yield without activation, indicating that the nitric acid erosion was very serious during the activation process, but it not means the porosity of A-1 was developed largely, The activation yield is not directly proportional to the pore development.

Yield of pyrolysis without activation (a) and pyrolysis with activation (b).
3.3 Compressive strength
The compressive strength of coal-based material is preferably above 1.5 MPa. The minimum value of 1.161 MPa was not available for electrode materials. Additive ratio increased from group 1 to group 3 in Figure 3, It was not shown the clearly relationship between the DCLR addition ratio and compressive strength value. The proportion of DCLR affected the compressive strength of the samples, but also affected by other factors at the same time.

The compressive strength of samples.
3.4 Statistical analysis
The stepwise regression method was chosen to analyze the experimental data in Table 6. The quadratic regression surface model was established after eliminating the non-significant items. The model for Iodine number is calculated by the obtained quadratic regression equation given by Eq. 4.
Analysis of variance for the regression model (R2=0.9997).
| source | Df | Sum of square | Mean square | F value | P-value |
|---|---|---|---|---|---|
| Model | 8 | 15217.391 | 1902.17 | 4325.056 | 0.0118 |
| Error | 1 | 0.440 | 0.44 | ||
| Total | 9 | 15217.831 |
where: X1, X2, and X3 are equal to (ratio-0.3)/0.1, (final temperature-800)/100 and (heating rate-10)/5.
According to the analysis of variance, this equation is suitable for expressing the model. The R2=0.9997 and the low P-value (0.0118) indicated that the fitting models was reasonable. Hence, the model can be used to analyze and optimize the process parameters of coal-based electrode material.
In Table 7, the significant sequence for these key factors is X2>X3>X1, the effects of the quadratic term X12, X1X2, X2X3, X32 on the number are also significant. This means that the final pyrolysis temperature is the most critical factor, and the interaction of three factors among them is not a simple linear relationship.
Significance test for the regression coefficients.
| source | Df | Sum of square | F value | P-value |
|---|---|---|---|---|
| X1 | 1 | 436.4298 | 992.3296 | 0.0202* |
| X2 | 1 | 8977.7860 | 20413.19 | 0.0045* |
| X3 | 1 | 1687.3849 | 3836.681 | 0.0103* |
| X12 | 1 | 99.7850 | 226.8856 | 0.0422* |
| X1X2 | 1 | 370.3940 | 842.1810 | 0.0219* |
| X1X3 | 1 | 3.2252 | 7.3333 | 0.2252 |
| X2X3 | 1 | 329.5877 | 749.3981 | 0.0232* |
| X32 | 1 | 375.3104 | 853.3597 | 0.0218* |
“*” means significant influence factor
3.5 Optimization and verification
The above response surface quadratic model was applied to explore the best combination of three factors. The changes of iodine number with different selection of variables are shown in the predict profile as Figure 4.

The predicted profile of higher IN.
According to the parameters in the prediction to obtain higher IN of coal-based electrode materials, 3 parallel samples (A-11, A-12, A-13) were performed in laboratory and the iodine number was 398.70 mg·g-1, 403.14 mg·g-1 and 401.22 mg·g-1 respectively, and the average IN was 401.02 mg·g-1, it was improved compared to before. The compressive strength of A-12 was 2.01 MPa, The properties of A-12 were analyzed by several methods in the following content.
3.6 SEM analyze
No visible pore structure in the SEM image (Figure 5) of each sample except for Sample of A-12. The volatile of pyrolysis gas and the nitric acid erosion created and cleaned the pores. The main contribution of the iodine number comes from micropores. The pores in the 500-1000x SEM image are macropores. The higher iodine number of the A-12 should be the result of an increase in the number of micropores and macropores.

(Continued).

(Continued).

The SEM images of samples (a) A–1, (b) A–2, (c) A–3, (d) A–4, (e) A–5, (f) A–6, (g) A–7, (h) A–8, (i) A–9, (j) A–10, (k) A–12 × 500, and (l) A–12 × 1000.
3.7 FT-IR analyze
Seven absorption peaks were observed in Figure 6 at 3445, 2925, 2850, 1750, 1630, 1400, and 1100 cm-1, which correspond to the stretching vibration of hydroxyl (-OH), stretching vibration of -CH2-, stretching vibration of C-H, stretching vibration of carbonyl (C=O) at 1750 and 1630, deformation vibration of -CH2-, and out-of-plane vibration of C-O, respectively. The 3rd area is the fingerprint area, which is generally used to support the determination of functional groups in other areas. The observation of -OH indicated that the pyrolysis and activation can promote the reactivity of -OH, facilitating the detachment to produce H2O or conversion to other oxygen-containing functional groups, such as C=O, C-O, and others. The absorption peaks in 1st area were considered as aldehyde compounds and the absorption peaks in 2nd area were considered as aromatic compounds in this study. More oxygen-containing functional groups have better wettability and are beneficial for subsequent applications.

The FT-IR curve of coal-based electrode material.
3.8 Pyrolysis mechanism
The pyrolysis process including several stages, the adsorbed H2O, N2 and CO2 on the surface of the raw material were released at lower temperature. Several weak chemical bonds in SJC and DCLR began to break at higher temperature stage, resulting in a small amount of CO2, N2 and H2O, also with some low-boiling substances. When the temperature raised to 400 °C-600 °C, an intense pyrolysis reaction occurred, and the number of colloids substantially increased. The colloids contain a large amount of asphaltene and preasphaltene, which were formed by hydrogen bonding between acid substances, such as phenolic hydroxyl groups, and alkaline substances, such as heterocyclic oxygen compounds or ether oxygen. When the gas volatilized from the coal matrix left the pore behind. And the pore structure improved the adsorption performance as well as the iodine number. The possible chemical reactions involved as follows (Ph/Ph′ means benzene ring).
3.9 Cyanide wastewater treatment
The coal-based electrode material was used as the anode and cathode, and the applied voltage was 4 V. Commercially activated carbon was used as a particle electrode, and the cyanide wastewater was treated in a three-dimensional electrode system for 5 h. Wastewater treatment experiment used three pieces of coal-based electrode sheets to form a double electric field effect. The results are shown in Table 8.
Removal rate of each ion in cyanide wastewater with voltage of 4V.
| ion | CNT | CN– | Cu | Zn | SCN– |
|---|---|---|---|---|---|
| concentration/(mg/g) | 474.67 | 83.76 | 118.39 | 156.02 | 63.96 |
| Removal rate/% | 72.54 | 77.19 | 78.32 | 65.80 | 75.41 |
Seen from Table 8, the removal rate of each ion in the cyanide wastewater reached 72% or more except Zn ion. At voltages of 4 V, both electro-adsorption and electrodeposition existed in the system. Larger voltages give more driving forces to the ions. As long as the ion size matches the pore size of the coal-based electrode material, the adsorption removal effect can be achieved. At the same time, the oxidation-reduction reaction of the upper and negative anodes was the main source of deposition. Therefore, the removal rate of ion in the waste water is high, but the improvement is still needed, and further optimization is allowed in subsequent experiments.
4 Conclusions
Coal-based electrode materials were successfully prepared with the suitable addition ratio of SJC and DCLR. The final pyrolysis temperature was the most significant factor analyzed by JMP software. And the significance sequence was C > B > A. The interaction of parameters is found to be significant and needs to be considered in the empirical equation, giving an excellent estimation. The iodine adsorption value and compressive strength value of sample prepared with the optimized parameters was 403.14 mg·g-1 and 2.01 MPa respectively, giving a high porosity and a high surface area. The oxygen-containing functional groups on coal-based electrode materials were beneficial for wettability in order to treat the wastewater. The removal rate of each ion in the three-dimensional electrode system was high. The removal rates of CNT, CN-, Cu, Zn, and SCN- in wastewater were 72.54%, 77.19%, 78.32%, 65.80%, and 75.41%, respectively.
Acknowledgements
The authors acknowledge the financial support by Natural Science Foundation of Shaanxi Province of China (2019JM-542), National Natural Science Foundation of China (51774227), Natural Science Foundation of Shaanxi Province of China (2018JZ5011).
List of abbreviations
- ad
air-dry basis
- Mad
Moisture
- Aad
Ash content
- Vad
Volatiles
- FCad
Fixed Carbon
- Cad
Carbon
- Oad
Oxygen (by difference)
- Had
Hydrogen
- Nad
Nitrogen
- St,ad
total Sulfur
- *FCad =
100% – (Vad + Aad + Mad)
- *Oad =
100% – (Cad + Had + Nad + Sad + Aad + Mad)
- CNT
Total cyanide
- CN-
Free cyanide
- SCN-
Thiocyanate
- Cu
Cupper
- Zn
Zinc
- A
additive ratio
- B
heating rate
- C
final pyrolysis temperature
- CS
Compressive strength, MPa
- IN
Iodine number, mg/g
- R2
Correlation coefficient
- Φ
Diameter
References
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© 2019 Su et al., published by De Gruyter
This work is licensed under the Creative Commons Attribution 4.0 Public License.
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- Green and eco-friendly synthesis of Co3O4 and Ag-Co3O4: Characterization and photo-catalytic activity
- Adsorption optimized of the coal-based material and application for cyanide wastewater treatment
- Aloe vera leaf extract mediated green synthesis of selenium nanoparticles and assessment of their In vitro antimicrobial activity against spoilage fungi and pathogenic bacteria strains
- Waste phenolic resin derived activated carbon by microwave-assisted KOH activation and application to dye wastewater treatment
- Direct ethanol production from cellulose by consortium of Trichoderma reesei and Candida molischiana
- Agricultural waste biomass-assisted nanostructures: Synthesis and application
- Biodiesel production from rubber seed oil using calcium oxide derived from eggshell as catalyst – optimization and modeling studies
- Study of fabrication of fully aqueous solution processed SnS quantum dot-sensitized solar cell
- Assessment of aqueous extract of Gypsophila aretioides for inhibitory effects on calcium carbonate formation
- An environmentally friendly acylation reaction of 2-methylnaphthalene in solvent-free condition in a micro-channel reactor
- Aegle marmelos phytochemical stabilized synthesis and characterization of ZnO nanoparticles and their role against agriculture and food pathogen
- A reactive coupling process for co-production of solketal and biodiesel
- Optimization of the asymmetric synthesis of (S)-1-phenylethanol using Ispir bean as whole-cell biocatalyst
- Synthesis of pyrazolopyridine and pyrazoloquinoline derivatives by one-pot, three-component reactions of arylglyoxals, 3-methyl-1-aryl-1H-pyrazol-5-amines and cyclic 1,3-dicarbonyl compounds in the presence of tetrapropylammonium bromide
- Preconcentration of morphine in urine sample using a green and solvent-free microextraction method
- Extraction of glycyrrhizic acid by aqueous two-phase system formed by PEG and two environmentally friendly organic acid salts - sodium citrate and sodium tartrate
- Green synthesis of copper oxide nanoparticles using Juglans regia leaf extract and assessment of their physico-chemical and biological properties
- Deep eutectic solvents (DESs) as powerful and recyclable catalysts and solvents for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones
- Biosynthesis, characterization and anti-microbial activity of silver nanoparticle based gel hand wash
- Efficient and selective microwave-assisted O-methylation of phenolic compounds using tetramethylammonium hydroxide (TMAH)
- Anticoagulant, thrombolytic and antibacterial activities of Euphorbia acruensis latex-mediated bioengineered silver nanoparticles
- Volcanic ash as reusable catalyst in the green synthesis of 3H-1,5-benzodiazepines
- Green synthesis, anionic polymerization of 1,4-bis(methacryloyl)piperazine using Algerian clay as catalyst
- Selenium supplementation during fermentation with sugar beet molasses and Saccharomyces cerevisiae to increase bioethanol production
- Biosynthetic potential assessment of four food pathogenic bacteria in hydrothermally silver nanoparticles fabrication
- Investigating the effectiveness of classical and eco-friendly approaches for synthesis of dialdehydes from organic dihalides
- Pyrolysis of palm oil using zeolite catalyst and characterization of the boil-oil
- Azadirachta indica leaves extract assisted green synthesis of Ag-TiO2 for degradation of Methylene blue and Rhodamine B dyes in aqueous medium
- Synthesis of vitamin E succinate catalyzed by nano-SiO2 immobilized DMAP derivative in mixed solvent system
- Extraction of phytosterols from melon (Cucumis melo) seeds by supercritical CO2 as a clean technology
- Production of uronic acids by hydrothermolysis of pectin as a model substance for plant biomass waste
- Biofabrication of highly pure copper oxide nanoparticles using wheat seed extract and their catalytic activity: A mechanistic approach
- Intelligent modeling and optimization of emulsion aggregation method for producing green printing ink
- Improved removal of methylene blue on modified hierarchical zeolite Y: Achieved by a “destructive-constructive” method
- Two different facile and efficient approaches for the synthesis of various N-arylacetamides via N-acetylation of arylamines and straightforward one-pot reductive acetylation of nitroarenes promoted by recyclable CuFe2O4 nanoparticles in water
- Optimization of acid catalyzed esterification and mixed metal oxide catalyzed transesterification for biodiesel production from Moringa oleifera oil
- Kinetics and the fluidity of the stearic acid esters with different carbon backbones
- Aiming for a standardized protocol for preparing a process green synthesis report and for ranking multiple synthesis plans to a common target product
- Microstructure and luminescence of VO2 (B) nanoparticle synthesis by hydrothermal method
- Optimization of uranium removal from uranium plant wastewater by response surface methodology (RSM)
- Microwave drying of nickel-containing residue: dielectric properties, kinetics, and energy aspects
- Simple and convenient two step synthesis of 5-bromo-2,3-dimethoxy-6-methyl-1,4-benzoquinone
- Biodiesel production from waste cooking oil
- The effect of activation temperature on structure and properties of blue coke-based activated carbon by CO2 activation
- Optimization of reaction parameters for the green synthesis of zero valent iron nanoparticles using pine tree needles
- Microwave-assisted protocol for squalene isolation and conversion from oil-deodoriser distillates
- Denitrification performance of rare earth tailings-based catalysts
- Facile synthesis of silver nanoparticles using Averrhoa bilimbi L and Plum extracts and investigation on the synergistic bioactivity using in vitro models
- Green production of AgNPs and their phytostimulatory impact
- Photocatalytic activity of Ag/Ni bi-metallic nanoparticles on textile dye removal
- Topical Issue: Green Process Engineering / Guest Editors: Martine Poux, Patrick Cognet
- Modelling and optimisation of oxidative desulphurisation of tyre-derived oil via central composite design approach
- CO2 sequestration by carbonation of olivine: a new process for optimal separation of the solids produced
- Organic carbonates synthesis improved by pervaporation for CO2 utilisation
- Production of starch nanoparticles through solvent-antisolvent precipitation in a spinning disc reactor
- A kinetic study of Zn halide/TBAB-catalysed fixation of CO2 with styrene oxide in propylene carbonate
- Topical on Green Process Engineering
Articles in the same Issue
- Regular Articles
- Studies on the preparation and properties of biodegradable polyester from soybean oil
- Flow-mode biodiesel production from palm oil using a pressurized microwave reactor
- Reduction of free fatty acids in waste oil for biodiesel production by glycerolysis: investigation and optimization of process parameters
- Saccharin: a cheap and mild acidic agent for the synthesis of azo dyes via telescoped dediazotization
- Optimization of lipase-catalyzed synthesis of polyethylene glycol stearate in a solvent-free system
- Green synthesis of iron oxide nanoparticles using Platanus orientalis leaf extract for antifungal activity
- Ultrasound assisted chemical activation of peanut husk for copper removal
- Room temperature silanization of Fe3O4 for the preparation of phenyl functionalized magnetic adsorbent for dispersive solid phase extraction for the extraction of phthalates in water
- Evaluation of the saponin green extraction from Ziziphus spina-christi leaves using hydrothermal, microwave and Bain-Marie water bath heating methods
- Oxidation of dibenzothiophene using the heterogeneous catalyst of tungsten-based carbon nanotubes
- Calcined sodium silicate as an efficient and benign heterogeneous catalyst for the transesterification of natural lecithin to L-α-glycerophosphocholine
- Synergistic effect between CO2 and H2O2 on ethylbenzene oxidation catalyzed by carbon supported heteropolyanion catalysts
- Hydrocyanation of 2-arylmethyleneindan-1,3-diones using potassium hexacyanoferrate(II) as a nontoxic cyanating agent
- Green synthesis of hydratropic aldehyde from α-methylstyrene catalyzed by Al2O3-supported metal phthalocyanines
- Environmentally benign chemical recycling of polycarbonate wastes: comparison of micro- and nano-TiO2 solid support efficiencies
- Medicago polymorpha-mediated antibacterial silver nanoparticles in the reduction of methyl orange
- Production of value-added chemicals from esterification of waste glycerol over MCM-41 supported catalysts
- Green synthesis of zerovalent copper nanoparticles for efficient reduction of toxic azo dyes congo red and methyl orange
- Optimization of the biological synthesis of silver nanoparticles using Penicillium oxalicum GRS-1 and their antimicrobial effects against common food-borne pathogens
- Optimization of submerged fermentation conditions to overproduce bioethanol using two industrial and traditional Saccharomyces cerevisiae strains
- Extraction of In3+ and Fe3+ from sulfate solutions by using a 3D-printed “Y”-shaped microreactor
- Foliar-mediated Ag:ZnO nanophotocatalysts: green synthesis, characterization, pollutants degradation, and in vitro biocidal activity
- Green cyclic acetals production by glycerol etherification reaction with benzaldehyde using cationic acidic resin
- Biosynthesis, characterization and antimicrobial activities assessment of fabricated selenium nanoparticles using Pelargonium zonale leaf extract
- Synthesis of high surface area magnesia by using walnut shell as a template
- Controllable biosynthesis of silver nanoparticles using actinobacterial strains
- Green vegetation: a promising source of color dyes
- Mechano-chemical synthesis of ammonia and acetic acid from inorganic materials in water
- Green synthesis and structural characterization of novel N1-substituted 3,4-dihydropyrimidin-2(1H)-ones
- Biodiesel production from cotton oil using heterogeneous CaO catalysts from eggshells prepared at different calcination temperatures
- Regeneration of spent mercury catalyst for the treatment of dye wastewater by the microwave and ultrasonic spray-assisted method
- Green synthesis of the innovative super paramagnetic nanoparticles from the leaves extract of Fraxinus chinensis Roxb and their application for the decolourisation of toxic dyes
- Biogenic ZnO nanoparticles: a study of blueshift of optical band gap and photocatalytic degradation of reactive yellow 186 dye under direct sunlight
- Leached compounds from the extracts of pomegranate peel, green coconut shell, and karuvelam wood for the removal of hexavalent chromium
- Enhancement of molecular weight reduction of natural rubber in triphasic CO2/toluene/H2O systems with hydrogen peroxide for preparation of biobased polyurethanes
- An efficient green synthesis of novel 1H-imidazo[1,2-a]imidazole-3-amine and imidazo[2,1-c][1,2,4]triazole-5-amine derivatives via Strecker reaction under controlled microwave heating
- Evaluation of three different green fabrication methods for the synthesis of crystalline ZnO nanoparticles using Pelargonium zonale leaf extract
- A highly efficient and multifunctional biomass supporting Ag, Ni, and Cu nanoparticles through wetness impregnation for environmental remediation
- Simple one-pot green method for large-scale production of mesalamine, an anti-inflammatory agent
- Relationships between step and cumulative PMI and E-factors: implications on estimating material efficiency with respect to charting synthesis optimization strategies
- A comparative sorption study of Cr3+ and Cr6+ using mango peels: kinetic, equilibrium and thermodynamic
- Effects of acid hydrolysis waste liquid recycle on preparation of microcrystalline cellulose
- Use of deep eutectic solvents as catalyst: A mini-review
- Microwave-assisted synthesis of pyrrolidinone derivatives using 1,1’-butylenebis(3-sulfo-3H-imidazol-1-ium) chloride in ethylene glycol
- Green and eco-friendly synthesis of Co3O4 and Ag-Co3O4: Characterization and photo-catalytic activity
- Adsorption optimized of the coal-based material and application for cyanide wastewater treatment
- Aloe vera leaf extract mediated green synthesis of selenium nanoparticles and assessment of their In vitro antimicrobial activity against spoilage fungi and pathogenic bacteria strains
- Waste phenolic resin derived activated carbon by microwave-assisted KOH activation and application to dye wastewater treatment
- Direct ethanol production from cellulose by consortium of Trichoderma reesei and Candida molischiana
- Agricultural waste biomass-assisted nanostructures: Synthesis and application
- Biodiesel production from rubber seed oil using calcium oxide derived from eggshell as catalyst – optimization and modeling studies
- Study of fabrication of fully aqueous solution processed SnS quantum dot-sensitized solar cell
- Assessment of aqueous extract of Gypsophila aretioides for inhibitory effects on calcium carbonate formation
- An environmentally friendly acylation reaction of 2-methylnaphthalene in solvent-free condition in a micro-channel reactor
- Aegle marmelos phytochemical stabilized synthesis and characterization of ZnO nanoparticles and their role against agriculture and food pathogen
- A reactive coupling process for co-production of solketal and biodiesel
- Optimization of the asymmetric synthesis of (S)-1-phenylethanol using Ispir bean as whole-cell biocatalyst
- Synthesis of pyrazolopyridine and pyrazoloquinoline derivatives by one-pot, three-component reactions of arylglyoxals, 3-methyl-1-aryl-1H-pyrazol-5-amines and cyclic 1,3-dicarbonyl compounds in the presence of tetrapropylammonium bromide
- Preconcentration of morphine in urine sample using a green and solvent-free microextraction method
- Extraction of glycyrrhizic acid by aqueous two-phase system formed by PEG and two environmentally friendly organic acid salts - sodium citrate and sodium tartrate
- Green synthesis of copper oxide nanoparticles using Juglans regia leaf extract and assessment of their physico-chemical and biological properties
- Deep eutectic solvents (DESs) as powerful and recyclable catalysts and solvents for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones
- Biosynthesis, characterization and anti-microbial activity of silver nanoparticle based gel hand wash
- Efficient and selective microwave-assisted O-methylation of phenolic compounds using tetramethylammonium hydroxide (TMAH)
- Anticoagulant, thrombolytic and antibacterial activities of Euphorbia acruensis latex-mediated bioengineered silver nanoparticles
- Volcanic ash as reusable catalyst in the green synthesis of 3H-1,5-benzodiazepines
- Green synthesis, anionic polymerization of 1,4-bis(methacryloyl)piperazine using Algerian clay as catalyst
- Selenium supplementation during fermentation with sugar beet molasses and Saccharomyces cerevisiae to increase bioethanol production
- Biosynthetic potential assessment of four food pathogenic bacteria in hydrothermally silver nanoparticles fabrication
- Investigating the effectiveness of classical and eco-friendly approaches for synthesis of dialdehydes from organic dihalides
- Pyrolysis of palm oil using zeolite catalyst and characterization of the boil-oil
- Azadirachta indica leaves extract assisted green synthesis of Ag-TiO2 for degradation of Methylene blue and Rhodamine B dyes in aqueous medium
- Synthesis of vitamin E succinate catalyzed by nano-SiO2 immobilized DMAP derivative in mixed solvent system
- Extraction of phytosterols from melon (Cucumis melo) seeds by supercritical CO2 as a clean technology
- Production of uronic acids by hydrothermolysis of pectin as a model substance for plant biomass waste
- Biofabrication of highly pure copper oxide nanoparticles using wheat seed extract and their catalytic activity: A mechanistic approach
- Intelligent modeling and optimization of emulsion aggregation method for producing green printing ink
- Improved removal of methylene blue on modified hierarchical zeolite Y: Achieved by a “destructive-constructive” method
- Two different facile and efficient approaches for the synthesis of various N-arylacetamides via N-acetylation of arylamines and straightforward one-pot reductive acetylation of nitroarenes promoted by recyclable CuFe2O4 nanoparticles in water
- Optimization of acid catalyzed esterification and mixed metal oxide catalyzed transesterification for biodiesel production from Moringa oleifera oil
- Kinetics and the fluidity of the stearic acid esters with different carbon backbones
- Aiming for a standardized protocol for preparing a process green synthesis report and for ranking multiple synthesis plans to a common target product
- Microstructure and luminescence of VO2 (B) nanoparticle synthesis by hydrothermal method
- Optimization of uranium removal from uranium plant wastewater by response surface methodology (RSM)
- Microwave drying of nickel-containing residue: dielectric properties, kinetics, and energy aspects
- Simple and convenient two step synthesis of 5-bromo-2,3-dimethoxy-6-methyl-1,4-benzoquinone
- Biodiesel production from waste cooking oil
- The effect of activation temperature on structure and properties of blue coke-based activated carbon by CO2 activation
- Optimization of reaction parameters for the green synthesis of zero valent iron nanoparticles using pine tree needles
- Microwave-assisted protocol for squalene isolation and conversion from oil-deodoriser distillates
- Denitrification performance of rare earth tailings-based catalysts
- Facile synthesis of silver nanoparticles using Averrhoa bilimbi L and Plum extracts and investigation on the synergistic bioactivity using in vitro models
- Green production of AgNPs and their phytostimulatory impact
- Photocatalytic activity of Ag/Ni bi-metallic nanoparticles on textile dye removal
- Topical Issue: Green Process Engineering / Guest Editors: Martine Poux, Patrick Cognet
- Modelling and optimisation of oxidative desulphurisation of tyre-derived oil via central composite design approach
- CO2 sequestration by carbonation of olivine: a new process for optimal separation of the solids produced
- Organic carbonates synthesis improved by pervaporation for CO2 utilisation
- Production of starch nanoparticles through solvent-antisolvent precipitation in a spinning disc reactor
- A kinetic study of Zn halide/TBAB-catalysed fixation of CO2 with styrene oxide in propylene carbonate
- Topical on Green Process Engineering