Influence of carbon sources on the performance of carbon-coated nano-silicon

Silicon-based material is an important anode material for next-generation lithium-ion batteries.In order to overcome its shortcomings,carbon coating is often employed to improve the electrochemical performance.However,the carbon source,carbon content,and different contact and mixing schemes between carbon sources and silicon are all complex factors and need to be clarified.In this study,nano-silicon is coated by the chemical vapor deposition method using different carbon sources,such as acetylene,methane,propane,and propylene.Carbon content after coating is designed to stay at the same level to reduce the experimental error.Results show the sample with higher conductivity provides higher cycle performance.Propylene is the best choice of the four carbon sources studied in this work.These results indicate that the selection of the carbon source is an important factor that plays a significant role in electrochemical performance.

Production and application of a novel bioflocculant by multiple-microorganism consortia using brewery wastewater as carbon source

The flocculating activity of a novel bioflocculant MMF1 produced by multiple-microorganism consortia MM1 was investigated. MM1 was composed of strain BAFRT4 identified as Staphylococcus sp. and strain CYGS1 identified as Pseudomonas sp. The flocculating activity of MMF1 isolated from the screening medium was 82.9%, which is remarkably higher than that of the bioflocculant produced by either of the strains under the same condition. Brewery wastewater was also used as the carbon source for MM1, and the cost-effective production medium for MM1 mainly comprised 1.0 L brewery water （chemical oxygen demand （COD） 5000 mg/L）, 0.5 g/L urea, 0.5 g/L yeast extract, and 0.2 g/L （NH4）2SO4. The optimal conditions for the production of MMF1 was inoculum size 2%, initial pH 6.0, cultivating temperature 30℃, and shaking speed 160 r/min, under which the flocculating activity of the MMF1 reached 96.8%. Fifteen grams of purified bioflocculant could be recovered from 1.0 L of fermentation broth. MMF1 was identified as a macromolecular substance containing both protein and polysaccharide. It showed good flocculating performance in treating indigotin printing and dyeing wastewater, and the maximal removal efficiencies of COD and chroma were 79.2% and 86.5%, respectively.

Effect of carbon source on the denitrification in constructed wetlands

The ability of constructed wetlands with different plants in nitrate removal were investigated. The factors promoting the rates of denitrification including organic carbon, nitrate load, plants in wetlands, pH and water temperature in field were systematically investigated. The results showed that the additional carbon source （glucose） can remarkably improve the nitrate removal ability of the constructed wetland. It demonstrated that the nitrate removal rate can increase from 20% to more than 50% in summer and from 10% to 30% in winter, when the nitrate concentration was 30-40 rag/L, the retention time was 24 h and 25 mg/L dissolved organic carbon （DOC） was ploughed into the constructed wetland. However, the nitrite in the constructed wetland accumulated a little with the supply of the additional carbon source in summer and winter, and it increased from 0.15 to 2 mg/L in the effluent. It was also found that the abilities of plant in adjusting pH and temperature can result in an increase of denitrification in wetlands. The seasonal change may also impact the denitrification.

Effect of carbon source and nitrate concentration on denitrifying phosphorus removal by DPB sludge

Effect of added carbon source and nitrate concentration on the denitrifying phosphorus removal by DPB sludge was systematically studied using batch experiments, at the same time the variation of ORP was investigated. Results showed that the denitrifying and phosphorus uptake rate in anoxic phase increased with the high initial anaerobic carbon source addition. However once the initial COD concentration reached a certain level, which was in excess to the PHB saturation of poly-P bacteria, residual COD carried over to anoxic phase inhibited the subsequent denitrifying phosphorus uptake. Simultaneously, phosphate uptake continued until all nitrate was removed, following a slow endogenous release of phosphate. High nitrate concentration in anoxic phase increased the initial denitrifying phosphorus rate. Once the nitrate was exhausted, phosphate uptake changed to release. Moreover, the time of this turning point occurred later with the higher nitrate addition. On the other hand, through on-line monitoring the variation of the ORP with different initial COD concentration, it was found ORP could be used as a control parameter for phosphorus release, but it is impossible to utilize ORP for controlling the denitrificaion and anoxic phosphorus uptake operations.

Analysis of phosphate-accumulating organisms cultivated under different carbon sources with polymerase chain reaction-denaturing gradient gel electrophoresis assay

To investigate the microbial communities of microorganisms cultivated under different carbon sources, three sequencing batch reactors were operated. They were supplied with sewage, glucose and sodium acetate as carbon sources respectively and showed high phosphorus removal performance. The results of denaturing gradient gel electrophoresis(DGGE) of polymerase chain reaction-amplified(PCR) 16S rDNA fragments demonstrated that β-protebacteria, Actinomyces sp. and γ-protebacteria only exited in 1# reactor. The microbiological diversity of 1# reactor exceeded the other two reactors. Flavobacterium, Bacillales, Actinomyces, Actinobacteridae and uncultured bacteria(AF527584, AF502204, AY592749, AB076862, AJ619051, AF495454 and AY133070) could be detected in the biological phosphorus removal reactors.

Effects of carbon sources and temperature on the formation and structural characteristics of food-related Staphylococcus epidermidis biofilms

Biofilms are a constant concern in the food industry;understanding the effect of environmental conditions on biofilm formation is essential to develop effective control strategies.Therefore,this study was conducted to investigate biofilms formation by Staphylococcus epidermidis under various conditions.Biofilms were cultured in nutrient broth containing different carbon source concentrations(0–10 mg/mL)on polystyrene surfaces for 32 h of incubation at 37℃or 55℃,with quantification and enumeration at 8,16,24 and 32 h.S.epidermidis developed biofilms under all tested conditions;achieved the highest yield of biofilm biomass at 2.5 mg/mL for all carbon sources at 37℃.The highest efficiency of extracellular polymeric substance(EPS)molecule production occurred under glucose availability in the growth environment,with a higher yield of biomass and a significantly smaller number of metabolically active cells than under other tested conditions.A condensed ball-shaped structure was observed under the lactose condition.Meanwhile,biofilms in the presence of maltose showed mainly opaque thick rich colonies,while a compact multilayered-shaped structure was exhibited under both glucose and sucrose conditions.These results contribute to a better understanding of the biofilm formation by S.epidermidis in order to reduce contamination and recontamination in the food industry.

Differences in carbon source usage by dental plaque in children with and without early childhood caries

Early childhood caries （ECC） is a considerable pediatric and public health problem worldwide. Preceding studies have focused primarily on bacterial diversity at the taxonomic level. Although these studies have provided significant information regarding the connection between dental caries and oral micmbiomes, further comprehension of this microbial community＇s ecological relevance is limited. This study identified the carbon source metabolic differences in dental plaque between children with and without ECC. We compared the microbial community functional diversity in 18 caries-free subjects with 18 severe ECC patients based on sole carbon source usage using a Biolog assay. The anaerobic microbial community in the ECC patients displayed greater metabolic activity than that of the control group. Specific carbon source metabolism differed significantly between the two groups. Subjects from the two groups were well distinguished by cluster and principal component analyses based on discriminative carbon sources. Our results implied that the microbial functional diversity between the ECC patients and healthy subjects differed significantly. In addition, the Biolog assay furthered our understanding of oral microbiomes as a composite of functional abilities, thus enabling us to identify the ecologically relevant functional differences among oral microbial communities.

Direct Synthesis of Co-doped Graphene on Dielectric Substrates Using Solid Carbon Sources

Direct synthesis of high-quality doped graphene on dielectric substrates without transfer is highly desired for simplified device processing in electronic applications.However,graphene synthesis directly on substrates suitable for device applications,though highly demanded,remains unattainable and challenging.Here,a simple and transfer-free synthesis of high-quality doped graphene on the dielectric substrate has been developed using a thin Cu layer as the top catalyst and polycyclic aromatic hydrocarbons as both carbon precursors and doping sources.N-doped and N,F-co-doped graphene have been achieved using TPB and F16Cu Pc as solid carbon sources,respectively.The growth conditions were systematically optimized and the as-grown doped graphene were well characterized.The growth strategy provides a controllable transfer-free route for high-quality doped graphene synthesis,which will facilitate the practical applications of graphene.

Flame Retardant Finishing of Poly(ethylene terephthalate) Fabric with a Carbon Source Containing DOPO Derivative

9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide( DOPO)-based flame retardant( DOPO-DOPC) which contains carbon source was used to improve the flame retardancy of poly( ethylene terephthalate)( PET) fabrics. The prepared DOPODOPC dispersion was applied onto PET fabrics via two kinds of processes,thermosol process and exhaustion process,and in the later using it alone or together with disperse dyes. The flame retardancy of PET fabrics was determined by limiting oxygen index( LOI) and vertical burning test. The results showed that DOPODOPC could obviously improve the flame retardancy of PET fabrics.The PET fabric treated by 60 g/L DOPO-DOPC dispersion via exhaustion process achieved an LOI value of 32. 3%,for example.The flame retardancy and dyeing performances showed that DOPODOPC dispersion could be used together with a part of disperse dyes in one bath. The thermal stability of DOPO-DOPC and the treated PET fabrics were investigated by thermogravimetric analysis( TGA). And the flame retardant mechanism of DOPO-DOPC treated PET fabrics was further investigated by pyrolysis-gas chromatography/mass spectrometry( Py-GC/MS), Fourier transform infrared spectroscopy( FTIR) and scanning electron microscopy( SEM).

Bohemian Microdiamonds:Diamond-forming Media and Carbon Source

The Variscan Bohemian Massif in Central Europe,resulting from continent-continent collision,was long considered a potential UHP terrain due to numerous occurrences of high-pressure granulites,eclogites and

Effects of Different Carbon Sources and NaBr-KCl on Synthesis of Ti(C,N)

Ti（ C, N） was synthesized with the starting materials of 76. 9% titania white and 23. 1% carbon black （graphite or activated carbon ）, or 40% titania white and 60% amylum, with or without 10% NaBr - KCl, dry moulding and carbon embedded firing at i 300 ℃ and 1 400 ℃ for 3 h, respectively. Phase composition and microstructure of the synthesized Ti （C, N） were analyzed by XRD, SEM and EPMA. Effects of different carbon sources and NaBr-KCl on the synthesis of Ti（ C, N） were investigated. The results show that： （1） Ti （C, N） can be synthesized by using carbon black, graphite, activated carbon or amylum as carbon source separately; （2） Additive NaBr - KCl is more favorable for accelerating the carbothermal reduction reaction using carbon black or amylum as carbon source; （3） In the presence of NaBr - KCl, particle size of the synthesized Ti（ C, N） is 5 -8μm using carbon black as carbon source fired at 1 300 ℃ for 3 h, while that is only 1 - 3 μm using graphite, activated carbon or amylum fired at 1 400 ℃ for 3 h.

Types of Countryside Carbon Source and Carbon Sink against the Background of Carbon Neutral and Corresponding Strategies

Countryside is rich in large-scale blue and green spaces such as woodland, farmland, grassland and water, which means a great potential of carbon sink. Rural architecture still has a long way to go in terms of low-carbon construction, which makes countryside carbon source and carbon sink significant in researches and practices of realizing objectives of carbon neutral. In view of the problems of current researches on rural carbon source and carbon sink, such as indistinct rural characteristics, incomplete system construction, this paper through sorting out these researches systematically classified the types of countryside carbon source and carbon sink, proposed corresponding strategies, made prospects on researches and practices of countryside carbon source and carbon sink, so as to provide references for future researches.

Nitrous oxide emission by denitrifying phosphorus removal culture using polyhydroxyalkanoates as carbon source

Nitrous oxide （N2O） emission has been reported to be enhanced during denitrification when internally-stored compounds are used as carbon sources. However, negligible N2O emissions have been detected in the few studies where polyhydroxyalkanoates （PHA） were specifically used. This study investigated and compared the potential enhancement of N2O production, based on utilization of an internally-stored polymer and external carbon （acetate） by a denitrifying phosphorus removal culture. Results indicated that at relatively low chemical oxygen demand-to-nitrogen （COD/N） ratios, more nitrite was reduced to N2O in the presence of an external carbon source as compared to an internal carbon source （PHA）. At relatively higher COD/N ratios, similar N2O reduction rates were obtained in all cases regardless of the type of carbon source available. N2O reduction rates were, however, generally higher in the presence of an internal carbon source. Results from the study imply that when the presence of an external carbon source is not sufficient to support denitrification, it is likely competitively utilized by different metabolic pathways of denitrifying polyphosphate accumulating organisms （DPAOs） and other ordinary denitfifiers. This study also reveals that the consumption of PHA is potentially the rate-limiting step for N2O reduction during denitrification.

Starch/polyvinyl alcohol blended materials used as solid carbon source for tertiary denitrification of secondary efuent

Starch/polyvinyl alcohol （PVA） blended materials for using as a solid carbon source （SCS） were prepared by blending PVA and gelatinized starch in an aqueous solution system, in which PVA served as framework material and starch as carbon source. The optimization of starch content and temperature effects were investigated. It was indicated that higher denitrification efficiency could be achieved with more starch in the materials. The average specific denitrification rates were 0.93, 0.66, 0.37 and 0.36 mg/（g·day） corresponding to starch content of 70%, 60%, 40% and 30% respectively at 37℃. The denitrification rates increased when operating temperature was raised from 23℃ to 30℃ and then 37℃. The mechanism of carbon release was analyzed incorporating the experimental results of abiotic release in deionized water. The organic carbon was mainly hydrolyzed by microbes, and the biological release efficiencies were at the range of 89.2% to 96.0%. A long-term experiment with a continuous flow reactor with SCS material containing 70% starch was conducted to gain some experience for practical application. When the influent nitrate concentration was in the range of 35.2 to 39.1 mg/L, hydraulic retention time of 4 hr, and operating temperature of 30℃, a nitrogen removal efficiency up to 94.6% and denitrification rate of 0.217 kg/（m3.day） was achieved. The starch-based materials developed in this study can be used as a solid carbon source for tertiary nitrogen removal from secondary effluent.

Removal of nitrate from groundwater by heterotrophic denitrification using the solid carbon source

Removal of nitrate from groundwater was investigated using biodegradable meal box(BMB) and poly(ε-caprolactone)(PCL) as carbon source and biofilm carrier.The experimental results show that nitrate in groundwater can be effectively removed using BMB and PCL as carbon source.Denitrification rates supported by BMB and PCL were 52.80 and 42.77 mg(NO3-N)/(m2h),respectively,at 30 ℃ and pH 7.5.The pH value of effluent ranged from 7 to 8,and NO2-N concentration was less than 0.1 mg/L.Compared with BMB,PCL could decrease nitrite accumulation;however,more significant influence of temperature on denitrification was observed for PCL as carbon source.Temperature constants for BMB and PCL were 0.045 and 0.068,respectively,at 10-30℃.Based on denitrification efficiency and cost,BMB is more suitable as a carbon source for denitrification of groundwater than PCL.

Initial carbon release characteristics, mechanisms and denitrification performance of a novel slow release carbon source

External carbon source addition is one of the effective methods for the treatment of wastewater with low carbon to nitrogen ratio(C/N). Compared with fast-release liquid carbon sources, slow-release solid carbon sources are more suitable for the denitrification process. A novel slow-release solid carbon source(corncob-polyvinyl alcohol sodium alginatepoly-caprolactone, i.e. CPSP) was prepared using corn cob(CC) and poly-caprolactone with polyvinyl alcohol sodium alginate as hybrid scaffold. The physical properties and carbon release characteristics of CPSP and three other carbon sources were compared. CPSP had stable framework and good carbon release performance, which followed the second order release equation. The formic acid, acetic acid, propionic acid and butyric acid released from CPSP accounted for 8.27% ± 1.66 %, 56.48% ± 3.71 %, 18.46% ± 2.69% and 16.79% ± 3.02% of the total released acids respectively. The start-up period of CPSP was shorter than that of the other carbon sources in denitrification experiment, and no COD pollution was observed in the start-up phase(25–72 h) and stable phase(73–240 hr). The composition and structure of the dissolved organic compounds released by CPSP and other carbon sources were analyzed by UV-Vis absorption spectroscopy and three-dimensional fluorescence spectroscopy,which indicated that CPSP was more suitable for denitrification than the other studied carbon sources.

Effects of different carbon sources on the removal of ciprofloxacin and pollutants by activated sludge:Mechanism and biodegradation

This research investigated the effects of ciprofloxacin(CIP)(0.5,5,and 20 mg/L)on SBR systems under different carbon source conditions.Microbial community abundance and structure were determined by quantitative PCR and high-throughput sequencing,respectively.The biodegradation production of CIP and possible degradation mechanism were also studied.Results showed that CIP had adverse effects on the nutrient removal from wastewater.Compared with sodium acetate,glucose could be more effectively used by microorganisms,thus eliminating the negative effects of CIP.Glucose stimulated the microbial abundance and increased the removal rate of CIP by 18%–24%.The mechanism research indicated that Proteobacteria and Acidobacteria had a high tolerance for CIP.With sodium acetate as a carbon source,the abundance of nitrite-oxidizing bacterial communities decreased under CIP,resulting in the accumulation of nitrite and nitrate.Rhodanobacter and Microbacterium played a major role in nitrification and denitrification when using sodium acetate and glucose as carbon sources.Dyella and Microbacterium played positive roles in the degradation process of CIP and eliminated the negative effect of CIP on SBR,which was consistent with the improved removal efficiency of pollutants.

Optimization of denitrifying phosphorus removal in a predenitrification anaerobic/anoxic/post-aeration+nitrification sequence batch reactor(pre-A_(2)NSBR)system:Nitrate recycling,carbon/nitrogen ratio and carbon source type

Because the efficiency of biological nutrient removal is always limited by the deficient carbon source for the low carbon/nitrogen(C/N)ratio in real domestic sewage,the denitrifying phosphorus removal(DNPR)was developed as a simple and efficient method to remove nitrogen and phosphorous.In addition,this method has the advantage of saving aeration energy while reducing the sludge production.In this context,a pre-denitrification anaerobic/anoxic/post-aeration+nitrification sequence batch reactor(pre-A_(2)NSBR)system,which could also reduce high ammonia effluent concentration in the traditional two-sludge DNPR process,is proposed in this work.The pre-A_(2)NSBR process was mainly composed of a DNPR SBR and a nitrifying SBR,operating as alternating anaerobic/anoxic/post-aeration+nitrification sequence.Herein,the long-term performance of different nitrate recycling ratios(0-300%)and C/N ratios(2.5-8.8),carbon source type,and functional microbial community were studied.The results showed that the removal efficiency of total inorganic nitrogen(TIN,including NH4^(+)-N,NO_(2)^(-)-N,and NO_(3)^(-)-N)gradually increased with the nitrate recycling ratios,and the system reached the highest DNPR efficiency of 94.45% at the nitrate recycling ratio of 300%.The optimum C/N ratio was around 3.9-7.3 with a nitrogen and phosphorus removal efficiency of 80.15%and 93.57%,respectively.The acetate was proved to be a high-quality carbon source for DNPR process.The results of fluorescence in situ hybridization(FISH)analysis indicated that nitrifiers and phosphorus accumulating organisms(PAOs)were accumulated with a proportion of 19.41%and 26.48%,respectively.

Burial fluxes and source apportionment of carbon in culture areas of Sanggou Bay over the past 200 years

In this study, we assessed the burial fluxes and source appointment of different forms of carbon in core sediments collected from culture areas in the Sanggou Bay, and preliminarily analyzed the reasons for the greater proportion of inorganic carbon burial fluxes （BFTIc）. The average content of total carbon （TC） in the Sanggou Bay was 2.14%. Total organic carbon （TOC） accounted for a small proportion in TC, more than 65% of which derived from terrigenous organic carbon （Ct）, and while the proportion of marine-derived organic carbon （Ca） increased significantly since the beginning of large-scale aquaculture. Total inorganic carbon （TIC） accounted for 60%-75% of TC, an average of which was 60%, with a maximum up to 90% during flourishing periods （1880-1948） of small natural shellfish derived from seashells inorganic carbon （SheU-IC）. The TC burial fluxes ranged from 31 g/（m2.a） to 895 g/（m2.a） with an average of 227 g/（m2.a）, which was dominated by TIC （about 70%）. Shell-IC was the main source of TIC and even TC. As the main food of natural shellfish, biogenic silica （BSi） negatively correlated with BFTIc through affecting shellfish breeding. BFTIc of Sta. S1, influenced greatly by the Yellow Sea Coastal Current, had a certain response to Pacific Decadal Oscillation （PDO） in some specific periods.

Production of Poly(3-Hydroxybutyrate-co-3-Hydroxyhexanoate) Using Aeromonas hydrophila 4AK4 Grown in Mixed Carbon Source

Aeromonas hydrophila 4AK4 was grown on mixed substrates of soybean oil and lauric acid for the production of polyhydroxyalkanoate copolymer consisting of 3 hydroxybutyrate (3HB) and 3 hydroxyhexanoate (3HHx). A maximal poly(3 hydroxybutyrate co 3 hydroxyhexanoate) (PHBHHx) content of 49.13% in dry cells was obtained in a shake flask culture. PHBHHx of 6.26 g/L was produced in a fermentation experiment over 48 h on a sole carbon source containing 100 g/L soybean oil, while 12.40 g/L PHBHHx was produced on a mixed carbon source containing 80 g/L soybean and 20 g/L lauric acid over the same period of time, resulting in a polyhydroxyalkanoate (PHA) productivity of 0.25 g/(L·h). The results show that mixed carbon sources are suitable for industrialized production of PHBHHx from A. hydrophila 4AK4, as the mixed carbon sources also overcome the foaming problem that occurs when lauric acid is employed as a sole carbon source in PHBHHx production.