Direct conversion of apricot seeds into biodiesel.

Using edible lipids for biodiesel production has been criticized, causing biodiesel production from inedible food resources to be desirable. Lipid extraction must be prioritized to produce biodiesel using an acid/base-catalyzed transesterification process, but this conversion process suffers from technical reliability. Therefore, this study introduced non-catalytic conversion of oil-bearing biomass into biodiesel. Apricot seeds were used as a model compound (oil content 44.3 wt%). The non-catalytic transesterification of apricot seed oil recovered 98.28 wt% biodiesel at 360 °C for 1 min, while alkali-catalysis of apricot seed oil recovered 91.84 wt% at 63 °C for 60 min. The direct conversion of apricot seeds into biodiesel was attempted. The trends in the yields of biodiesel from apricot seeds and seed oil obtained by non-catalytic transesterification as a function of reaction temperature were similar. The yield of biodiesel from apricot seed was 43.06 wt%, suggesting that 97.20 wt% of lipids were converted into biodiesel.

Iron-modified phosphorus- and silicon-based biochars exhibited various influences on arsenic, cadmium, and lead accumulation in rice and enzyme activities in a paddy soil.

Contamination of paddy soils with potentially toxic elements (PTEs) has become a severe environmental issue. Application of functionalized biochar for rice cultivation has been proposed as an effective means to reduce environmental risks of these PTEs in paddy soils. This work was undertaken to seek the positive effects of a rice husk-derived silicon (Si)-rich biochar (Si-BC) and a pig carcass-derived phosphorus (P)-rich biochar (P-BC), as well as their Fe-modified biochars (Fe-Si-BC and Fe-P-BC) on the enzyme activity and PTE availability in an As-Cd-Pb-contaminated soil. A rice cultivation pot trial was conducted using these functionalized biochars as soil amendments for the alleviation of PTE accumulation in rice plants. Results showed that Si-BC decreased the concentrations of As in rice grain and straw by 59.4 % and 61.4 %, respectively, while Fe-Si-BC significantly (P < 0.05) enhanced plant growth, increasing grain yield (by 38.6 %). Fe-Si-BC significantly (P < 0.05) elevated Cd and Pb accumulation in rice plants. P-BC enhanced the activities of dehydrogenase, catalase, and urease, and reduced grain-Pb and straw-Pb by 49.3 % and 43.2 %, respectively. However, Fe-P-BC reduced plant-As in rice grain and straw by 12.2 % and 51.2 %, respectively, but increased plant-Cd and plant-Pb. Thus, Fe-modified Si- and P-rich biochars could remediate paddy soils contaminated with As, and enhance the yield and quality of rice. Application of pristine P-rich biochar could also be a promising strategy to remediate the Pb-contaminated paddy soils and limit Pb accumulation in rice.

Genetic and non-genetic tailoring of microalgae for the enhanced production of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) - A review.

The myriad health benefits associated with eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) laid the path for their application in the functional foods and nutraceutical industries. Fish being primarily exploited for extraction of EPA and DHA are unsustainable sources; thus, oleaginous microalgae turn out to be an alternative sustainable source. This review paper aims to provide the recent developments in the context of enhancing EPA and DHA production by utilising non-genetic tailoring and genetic tailoring methods. We have also summarized the legislation, public perception, and possible risks associated with the usage of genetically modified microalgae focusing on EPA and DHA production.

The beneficial and hazardous effects of selenium on the health of the soil-plant-human system: An overview.

Selenium (Se), which can be both hazardous and beneficial to plants, animals and humans, plays a pivotal role in regulating soil-plant-human ecosystem functions. The biogeochemical behavior of Se and its environmental impact on the soil-plant-human system has received broad attention in the last decades. This review provides a comprehensive understanding of Se biogeochemistry in the soil-plant-human system. The speciation, transformation, bioavailability as well as the beneficial and hazardous effects of Se in the soil-plant-human system are summarized. Several important aspects in Se in the soil-plant-human system are detailed mentioned, including (1) strategies for biofortification in Se-deficient areas and phytoremediation of soil Se in seleniferous areas; (2) factors affecting Se uptake and transport by plants; (3) metabolic pathways of Se in the human body; (4) the interactions between Se and other trace elements in plant and animals, in particular, the detoxification of heavy metals by Se. Important research hotspots of Se biogeochemistry are outlined, including (1) the coupling of soil microbial activity and the Se biogeochemical cycle; (2) the molecular mechanism of Se metabolic in plants and animals; and (3) the application of Se isotopes as a biogeochemical tracer in research. This review provides up-to-date knowledge and guidelines on Se biogeochemistry research.

CO2-cofed catalytic pyrolysis of tea waste over Ni/SiO2 for the enhanced formation of syngas.

To valorize tea waste (TW), catalytic pyrolysis was done as a practical measure for recovering energy as a form of syngas. Considering CO2 as a reactive gas medium in place of conventional pyrolysis gas, a sustainable pyrolysis platform was established. In addition, mechanistic effectiveness of CO2 on TW pyrolysis was examined. In the presence of CO2, homogeneous reaction with volatile organic compounds (VOCs) derived from TW pyrolysis contributed to CO formation. To enhance the formation of syngas at low pyrolysis temperature, catalytic pyrolysis over a Ni/SiO2 was investigated. The synergistic effects of Ni/SiO2 catalyst and CO2 promoted thermal cracking of VOCs and further homogeneous reaction with CO2, thereby resulting in the substantial enhancement (28 times more) of H2 and CO production than non-catalytic pyrolysis. It was also confirmed that CO2 could be considered a reactive gas medium to produce biochar (34-35 wt.% yield), having competitive porosity and surface area, in comparison to that from pyrolysis in N2. Therefore, CO2 can be employed to build a sustainable waste conversion platform for energy and biochar production through pyrolysis instead of using N2.

Enhanced bioaromatics synthesis via catalytic co-pyrolysis of cellulose and spent coffee ground over microporous HZSM-5 and HY.

Catalytic co-pyrolysis (CCP) of spent coffee ground (SCG) and cellulose over HZSM-5 and HY was characterized thermogravimetrically, and a catalytic pyrolysis of two samples was conducted using a tandem micro reactor that directly connected with gas chromatography-mass spectrometry. To access the more fundamental investigations on CCP, the effects of the zeolite pore structure, reaction temperature, in-situ/ex-situ reaction mode, catalyst to feedstock ratio, and the SCG and cellulose mixing ratio were experimentally evaluated. The temperature showing the highest thermal degradation rate of cellulose with SCG slightly delayed due to the interactions during the thermolysis of two samples. HZSM-5 in reference to HY produced more aromatic hydrocarbons from CCP. With respect to the reaction temperature, the formation of aromatic hydrocarbons increased with the pyrolytic temperature. Moreover, the in-situ/ex-situ reaction mode, catalyst/feedstock, and cellulose/SCG ratio were optimized to improve the aromatic hydrocarbon yield.

Increased biodegradability of low-grade coal wastewater in anaerobic membrane bioreactor by adding yeast wastes.

Demineralization is required in upgrading low-grade coal to serve as an alternative energy resource for the production of fuel and valuable chemicals but generates a large amount of low-grade coal wastewater (LCWW). The objective of this study was to investigate the effects of a co-substrate on an anaerobic membrane bioreactor (AnMBR) treating LCWW. CH4 was not produced during the operation fed by LCWW alone. When yeast wastes (YW) were supplemented, there was a gradual increase in the biodegradability of LCWW, achieving 182 CH4 mL/g COD with 58% COD removal efficiency. The analysis of physicochemical characteristics in the effluent of AnMBR, done by excitation-emission matrix (EEM) and size exclusion chromatography (SEC), showed that the proportion of soluble microbial products (SMPs) and aromatic group with high-molecular weight (>1 kDa) increased. Microbial analysis revealed that the increased dominance of bacteria Comamonas, Methanococcus, and Methanosarcina facilitated biodegradation of LCWW in the presence of YW.

Production of bio-oil from fast pyrolysis of biomass using a pilot-scale circulating fluidized bed reactor and its characterization.

To circumvent the adverse impacts arising from an excessive use of fossil fuels, bioenergy and chemical production from a carbon neutral resource (biomass) has drawn considerable attention over the last two decades. Among various technical candidates, fast pyrolysis of biomass has been considered as one of the viable technical routes for converting a carbonaceous material (biomass) into biocrude (bio-oil). In these respects, three biomass samples (i.e., sawdust, empty fruit bunch, and giant Miscanthus) were chosen as a carbon substrate for the pyrolysis process in this study. A pilot-scale circulating fluidized bed reactor was employed for the pyrolysis work, and biocrude from the fast pyrolysis process at 500 °C were characterized because the maximum yield of biocrude (60 wt% of the original sample mass) was achieved at 500 °C. The physico-chemical properties of biocrude were measured by the international standard/protocol (ASTM D7544 and/or EN 16900 test method) to harness biocrude as bioenergy and an initial feedstock for diverse chemicals. All measurements in this study demonstrated that the heating value, moisture content, and ash contents in biocrude were highly contingent on the type of biomass. Moreover, characterization of biocrude in this study significantly suggested that additional unit operations for char and metal removal must be conducted to meet the fuel standard in terms of biocrude as bioenergy.

Investigation into role of CO2 in two-stage pyrolysis of spent coffee grounds.

As a way of improving process efficiency of pyrolysis of waste biomass, the effect of carbon dioxide (CO2) on pyrolysis of spent coffee grounds (SCGs) was examined using a two-stage pyrolysis reactor consisting of a region with increasing temperature and an isothermal region. It was experimentally validated that CO2 accelerates thermal cracking of organic compounds formed during the pyrolysis of SCGs. The expedited thermal cracking attributed to employing CO2 in pyrolysis of SCGs led to changing pyrolytic products in gas, liquid, and solid phases. The production of gaseous carbon monoxide was increased when using CO2 as the pyrolysis medium. In liquid pyrolytic products, the formation of phenolic compounds was hindered in the CO2-assited pyrolysis. Biochar morphology (solid pyrolytic product) was also changed with different pyrolysis environments. This study shows that CO2 can help improve applicability of pyrolysis of waste biomass by modifying three phase pyrolytic products in a two-stage pyrolyzer.

Thermochemical conversion of cobalt-loaded spent coffee grounds for production of energy resource and environmental catalyst.

Thermochemical conversion of cobalt (Co)-loaded lignin-rich spent coffee grounds (COSCG) was carried out to find the appropriate pyrolytic conditions (atmospheric gas and pyrolytic time) for syngas production (H2 and CO) and fabricate Co-biochar catalyst (CBC) in one step. The use of CO2 as atmospheric gas and 110-min pyrolytic time was optimal for generation of H2 (∼1.6 mol% in non-isothermal pyrolysis for 50 min) and CO (∼4.7 mol% in isothermal pyrolysis for 60 min) during thermochemical process of COSCG. The physicochemical properties of CBC fabricated using optimized pyrolytic conditions for syngas production were scrutinized using various analytical instruments (FE-SEM, TEM, XRD, and XPS). The characterizations exhibited that the catalyst consisted of metallic Co and surface wrinkled carbon layers. As a case study, the catalytic capability of CBC was tested by reducing p-nitrophenol (PNP), and the reaction kinetics of PNP in the presence of CBC was measured from 0.04 to 0.12 s-1.

Ferric-enhanced chemical remediation of dredged marine sediment contaminated by metals and petroleum hydrocarbons.

Sediments nearby harbors are dredged regularly, and the sediments require the stringent treatment to meet the regulations on reuse and mitigate the environmental burdens from toxic pollutants. In this study, FeCl3 was chosen as an extraction agent to treat marine sediment co-contaminated with Cu, Zn, and total petroleum hydrocarbons (TPH). In chemical extraction process, the extraction efficiency of Cu and Zn by FeCl3 was compared with the conventional one using inorganic acids (H2SO4 and HCl). Despite the satisfactory level for extraction of Cu (78.8%) and Zn (73.3%) by HCl (0.5 M) through proton-enhanced dissolution, one critical demerit, particularly acidified sediment, led to the unwanted loss of Al, Fe, and Mg by dissolution. Moreover, the vast amount of HCl required the huge amounts of neutralizing agents for the post-treatment of the sediment sample via the washing process. Despite a low concentration, extraction of Cu (70.1%) and Zn (69.4%) was done by using FeCl3 (0.05 M) through proton-enhanced dissolution, ferric-organic matter complexation, and oxidative dissolution of sulfide minerals. Ferric iron (Fe3+) was reduced to ferrous iron (Fe2+) with sulfide (S2-) oxidation during FeCl3 extraction. In consecutive chemical oxidations using hydrogen peroxide (H2O2) and persulfate (S2O82-), the resultant ferrous iron was used to activate the oxidants to effectively degrade TPH. S2O82- using FeCl3 solution (molar ratio of ferrous to S2O82- is 19.8-198.3) removed 42.6% of TPH, which was higher than that by H2O2 (molar ratio of ferrous to H2O2 is 1.2-6.1). All experimental findings suggest that ferric is effectively accommodated to an acid washing step for co-contaminated marine sediments, which leads to enhanced extraction, cost-effectiveness, and less environmental burden.

Fabrication of magnetic biochar as a treatment medium for As(V) via pyrolysis of FeCl3-pretreated spent coffee ground.

This study investigated the preparation of magnetic biochar from N2- and CO2-assisted pyrolysis of spent coffee ground (SCG) for use as an adsorption medium for As(V), and the effects of FeCl3 pretreatment of SCG on the material properties and adsorption capability of the produced biochar. Pyrolysis of FeCl3-pretreated SCG in CO2 atmosphere produced highly porous biochar with its surface area ∼70 times greater than that produced in N2 condition. However, despite the small surface area, biochar produced in N2 showed greater As(V) adsorption capability. X-ray diffraction and X-ray photoelectron spectrometer analyses identified Fe3C and Fe3O4 as dominant mineral phases in N2 and CO2 conditions, with the former being much more adsorptive toward As(V). The overall results suggest functional biochar can be facilely fabricated by necessary pretreatment to expand the applicability of biochar for specific purposes.

Arsenic, chromium, molybdenum, and selenium: Geochemical fractions and potential mobilization in riverine soil profiles originating from Germany and Egypt.

The fractionation and potential mobilization of As, Cr, Mo, and Se in four floodplain soil profiles collected along the Nile (Egypt) and Wupper (Germany) Rivers were assessed using the BCR sequential extraction procedure. The concentrations of total and the geochemical fractions (acid soluble (F1), reducible (F2), oxidizable (F3), and residual (F4) fraction) of the elements were determined. The Wupper soils had the highest total concentrations (mg kg-1) of As (378) and Cr (2,797) while the Nile soils contained the highest total Mo (12) and Se (42). The residual fraction of As, Cr, Mo, and Se was dominant in the Nile soils suggesting the geogenic source of the elements in these soils. The residual fraction of As and Mo and the oxidizable fraction of Cr and Se were dominant in the Wupper soils. Among the non-residual fractions (potential mobile fractions; PMF = ∑F1-F3), the oxidizable fraction was dominant for Cr, Mo, and Se in the Nile soils and for Mo in the Wupper soils, while the reducible fraction was dominant for As in both soils. The PMF of As, Cr, and Se was higher in the Wupper than in the Nile soils which might reflect the anthropogenic sources of these elements in the Wupper soils, while the opposite was the case for the PMF of Mo. The high PMF of Se (87%), Cr (87%), and As (21%) in the Wupper soils suggested that a release of these toxic elements may happen which increase the potential environmental risks in the anthropogenically polluted soils.

Carbon dioxide assisted sustainability enhancement of pyrolysis of waste biomass: A case study with spent coffee ground.

This work mainly presents the influence of CO2 as a reaction medium in the thermo-chemical process (pyrolysis) of waste biomass. Our experimental work mechanistically validated two key roles of CO2 in pyrolysis of biomass. For example, CO2 expedited the thermal cracking of volatile organic compounds (VOCs) evolved from the thermal degradation of spent coffee ground (SCG) and reacted with VOCs. This enhanced thermal cracking behavior and reaction triggered by CO2 directly led to the enhanced generation of CO (∼ 3000%) in the presence of CO2. As a result, this identified influence of CO2 also directly led to the substantial decrease (∼ 40-60%) of the condensable hydrocarbons (tar). Finally, the morphologic change of biochar was distinctive in the presence of CO2. Therefore, a series of the adsorption experiments with dye were conducted to preliminary explore the physico-chemical properties of biochar induced by CO2.

Boosting the value of biodiesel byproduct by the non-catalytic transesterification of dimethyl carbonate via a continuous flow system under ambient pressure.

Transformation of coconut oil into biodiesel by using dimethyl carbonate (DMC) via a non-catalytic transesterification reaction under ambient pressure was investigated in this study. The non-catalytic transformation to biodiesel was achieved by means of a heterogeneous reaction between liquid triglycerides and gas phase DMC. The reaction was enhanced in the presence of porous material due to its intrinsic physical properties such as tortuosity and absorption/adsorption. The numerous pores in the material served as micro reaction chambers and ensured that there was enough contact time between the liquid triglycerides and the gaseous DMC, which enabled the completion of the transesterification. The highest fatty acid methyl esters (FAMEs) yield achieved was 98±0.5% within 1-2min at a temperature of 360-450°C under ambient pressure. The fast reaction rates made it possible to convert the lipid feedstock into biodiesel via a continuous flow system without the application of increased pressure. This suggested that the commonly used supercritical conditions could be avoided, resulting in huge cost benefits for biodiesel production. In addition, the high value of the byproduct from the transesterification of the lipid feedstock with DMC suggested that the production biodiesel using this method could be more economically competitive. Finally, the basic properties of biodiesel derived from the non-catalytic conversion of rapeseed oil with DMC were summarised.

Sequential co-production of biodiesel and bioethanol with spent coffee grounds.

The sequential co-production of bioethanol and biodiesel from spent coffee grounds was investigated. The direct conversion of bioethanol from spent coffee grounds was not found to be a desirable option because of the relatively slow enzymatic saccharification behavior in the presence of triglycerides and the free fatty acids (FFAs) found to exist in the raw materials. Similarly, the direct transformation of the spent coffee grounds into ethanol without first extracting lipids was not found to be a feasible alternative. However, the crude lipids extracted from the spent coffee grounds were themselves converted into fatty acid methyl ester (FAME) and fatty acid ethyl ester (FAEE) via the non-catalytic biodiesel transesterification reaction. The yields of bioethanol and biodiesel were 0.46 g g(-1) and 97.5±0.5%, which were calculated based on consumed sugar and lipids extracted from spent coffee grounds respectively. Thus, this study clearly validated our theory that spent coffee grounds could be a strong candidate for the production of bioethanol and biodiesel.