Lipid enhancement in microalgae by temporal phase separation:Use of indigenous sources of nutrients

Microalgae have been recommended as superior candidate for fuel production because of their advantages of higher photosynthetic efficiency, biomass & lipid productivity, and faster growth rate as compared to other energy crops. To meet up all these criteria, we have developed a continuous outdoor micro-algal raceway pond reactor(RPR) and a lab scale indoor tubular photo bioreactor(PBR) for biofuel production. An attempt to utilise indigenous sources of nutrients to improve the economics also revealed that micro-algal culturing can also be used as a mode of nutrient removal and water treatment. The photosynthetic rate and lipid production were enhanced by arresting daytime cell division and promoting night-time cell division. A 50% lipid improvement was observed for the particular algal consortia. Microscopic studies revealed that temporal phase separation could be achieved by adjusting nutrient distribution pattern. To monitor temporal phase separation, it is required to know DNA multiplication model. Quantification of g DNA in RPR confirmed that cell division happens during the night which positively affects the photosynthetic efficiency and lipid productivity of microalgae.

Study on an improved rotating microchannel separator in the intensification for demulsification and separation process

An improved rotating microchannel(IRM) separator was further explored in the intensification for demulsification and separation process. Oil-in-water(O/W) emulsion system of 2-ethylhexyl phosphoric acid-2-ethylhexyl ester(P507)–water without emulsifier was employed to evaluate the performance of the new equipment. In this experiment, the influence on demulsification separation process was explored by changing the geometrical structure and channel height of the microchannel and combining the liquid–liquid two-phase flow pattern, and the correlation general graph between demulsification efficiency and dimensionless parameters was established. The total demulsification effect of the IRM and the separation capacity of the clear organic phase recovered from demulsification are significantly improved. In addition, the liquid–liquid two-phase flow pattern of the clear organic phase after demulsification and the remaining emulsion in the IRM are observed and recorded by high-speed photography. The separation ability of organic phase from the upper outlet can be significantly improved when the total demulsification rate of IRM is up to 90%. There are 3 types and 6 kinds of flow patterns observed. The results demonstrated that the suitable demulsification performance is obtained when the liquid–liquid two-phase inside the IRM is in a parallel pattern. Finally, the relation map between total demulsification efficiency and the universal flow is drawn, which provides a basis for the accurate control of the IRM device.

A Z-scheme LaFeO_(3)-CuFe_(2)O4 composite for sulfate radical-based photocatalytic process:Synergistic effect and mechanism

The sulfate radical-based photocatalytic process is supposed to be the most promising way to degrade organic pollutants.However,the development of a suitable and efficient photocatalyst is very challenging.The 40LaFeO_(3)-CuFe_(2)O_(4)(40LFO-CFO)nanocomposite was constructed and its catalytic performance was studied using Rhodamine B(RhB)as the target pollutant.40LFO-CFO exhibited excellent RhB degradation by the persulfate(PS)-assisted photocatalytic process compared to the pristine LFO and CFO.The degradation rate constant for RhB by 40LFO-CFO in the Vis/PS system was 2.22h^(-1)which is 3.04 times and 5.05 times higher than the pristine LFO(0.73 h^(-1))and CFO(0.44h^(-1)),respectively.Furthermore,the trapping experiments and EPR spectra proved that h^(+) plays a leading role in the bleaching of RhB for the 40LFO-CFO/PS/Vis system.The enhanced photocatalytic oxidation activity of 40LFO-CFO could be attributed to the unique charge carriers flow in 40LFO-CFO due to the Z-scheme and the cooperation effect between photocatalysis and PS activation.The recycle tests confessed the stability of 40LFO-CFO.Additionally,the intermediates and products of RhB are detected by liquid chromatographymass spectrometry(LC-MS),and the photocatalytic degradation routes of RhB for the 40LFO-CFO/Vis/PS system were proposed.Moreover,the 40LFO-CFO nanocomposite has a superior catalytic performance for other organics,suggesting that it is a promising heterocatalyst because of its high catalytic activity and stability for the PS-assisted photocatalytic process.

Remarkable enhancement of gas selectivity on organosilica hybrid membranes using urea-modulated metal-organic framework nanoparticles

Metal-organic framework/organosilica hybrid membranes on tubular ceramic substrates have shown great potential for the implementation of membrane technology in practical gas separation projects due to their higher permeance compared to commercial polymers.However,the selectivities of the reported membranes are moderate.Here,we have incorporated urea-modulated metal-organic frameworks into organosilica membranes to greatly enhance its separation performance.The urea-modulated metal-organic frameworks exhibit less-defined edges of crystallographic facets and high defect density.They can be well-dispersed in the organosilica layer,which substantially suppresses the interfacial defects between metal-organic frameworks and organosilica,which is beneficial for improving the selectivity of membranes for gas separation.The results have shown that the enhanced ideal selectivity of H_(2)/CH_(4) was 165 and that of CO_(2)/CH_(4) was 43,with H_(2) permeance of about 1.25×10^(−6) mol·m^(−2)·s^(−1)·Pa^(−1) and CO_(2) permeance of 3.27×10^(−7) mol·m^(−2)·s^(−1)·Pa^(−1) at 0.2 MPa and 25℃.In conclusion,the high level of hybrid membranes can be used to separate H_(2)(or CO_(2))from the binary gas mixture H_(2)/CH_(4)(or CO_(2)/CH_(4)),which is important for gas separation in practical applications.Moreover,the simple and feasible modulation of metal-organic framework is a promising strategy to tune different metal-organic frameworks for membranes according to the actual demands.

Research on separation and enhancement of speech micro-vibration from macro motion

Based on the 1 550 nm all-fiber pulsed laser Doppler vibrometer(LDV) system independently developed by our laboratory, empirical mode decomposition(EMD) and optimally modified Log-spectral amplitude estimator(OM-LSA) algorithms are associated to separate the speech micro-vibration from the target macro motion. This combined algorithm compensates for the weakness of the EMD algorithm in denoising and the inability of the OM-LSA algorithm on signal separation, achieving separation and simultaneous acquisition of the macro motion and speech micro-vibration of a target. The experimental results indicate that using this combined algorithm, the LDV system can functionally operate within 30 m and gain a 4.21 d B promotion in the signal-to-noise ratio(SNR) relative to a traditional OM-LSA algorithm.

Simultaneous recovery of phosphorus and nitrogen from liquid digestate by vacuum membrane distillation with permeate fractional condensation

A vacuum membrane distillation(VMD)process with permeate fractional condensation on membrane downstream has been developed for simultaneous recovery of phosphorus and nitrogen from liquid digestate.The polytetrafluoroethylene(PTFE)membrane flux could reach 6000 g·m-2·h-1 with the rejection efficiency of total phosphorus(TP)over 0.99,under the condition of flowrate being 120 L·h-1 and temperature being 40°C.Membrane fouling occurred with a film of organics and microorganism deposited on the surface of the membrane.Membrane flux could be reversed after the membrane was rinsed by water.Higher feed temperature and flowrate could improve the membrane flux,while hardly affect the rejection efficiency of total phosphorus.The concentration of TP could reach 1600 mg·L-1 after membrane distillation,which is about 5 times of that in initial liquid digestate.On the downstream of the membrane,some of the permeate vapor was condensed under the vacuum condition and most of water was collected here.The remaining vapor enriched with total nitrogen(TN)was compressed and pumped to the atmospheric condition to condense.The TN concentration in atmospheric condensate was as high as 7000 mg·L-1 with the process separation factor for ammonia being enhanced to 114.

Sedimentation acceleration of remanent iron oxide by magnetic flocculation

Sedimentation based processes are widely used in industry to separate particles from a liquid phase. Since the advent of the ＂Nanoworld＂ the demand for effective separation technologies has rapidly risen, calling for the development of new separation concepts, one of which lies in hybrid separation using the superposition of a magnetic field for magnetic particles. Possible product portfolio of such separation consists of pigment production, nanomagnetics production for electronics and bio separation, A promising step in that direction is magnetic field enhanced cake filtration, which has by now progressed from batch to continuous ooeration. In sedimentation processes in a mass force field the settling behaviour of particles strongly depends on physico-chemical properties, concentration and size distribution of the particles. By adjusting the pH, the interparticle forces, in particular the electrostatic repulsion, can be manipulated. For remanent magnetic particles such as magnetite, pre-treatment in a magnetic field could lead to a change of interparticle interactions. By magnetizing the particles apart from van der Waals attraction and electrostatic repulsion, an additional potential is induced, the magnetic attraction, which could easily dominate the other potentials and result in agglomeration in the primary minimum. By sedimentation analysis, a wide spectrum of parameters like pH, magnetic field strength and concentration have been investigated. The results show a strong increase of sedimentation velocity by magnetic flocculation of the raw suspension. This leads to a rise in throughput due to the acceleration of sedimentation kinetics by imparting a non-chemical interaction to the physico-chemical properties in the feed stream of the separation apparatus.