Owing to the formation of aggregation and gelation during storage,certain proteins and peptides exhibit limited applications in aqueous protein food products.The purpose of this study was to investigate the influence ...Owing to the formation of aggregation and gelation during storage,certain proteins and peptides exhibit limited applications in aqueous protein food products.The purpose of this study was to investigate the influence of homogenization and xanthan gum addition on the dispersion stability of Mytilus edulis hydrolysate(PHM).High-pressure homogenization(HPH)at 360 and 40 bar in the first and second values,respectively,and adding xanthan gum at a concentration of 1 mg/mL showed significantly improvement on the stability of the PHM solution.PHM-xanthan gum solutions(PHMX)showed the highest polypeptide precipitation rate and turbidity retention rate compared with those of PHM.Moreover,the centrifugal precipitation rate of PHMX without HPH was higher than that of homogeneous PHMX.After HPH treatment at 400 bar,the percentage of smaller particles in PHM and PHMX was increased,the aqueous system became more uniform,and the fluorescence intensity reached its maximum.HPH pretreatment improved the polypeptide dispersion stability and turbidity retention rate of PHM and PHMX and reduced the fluorescence intensity.The interactions of xanthan gum and polypeptide render the network microstructure more uniform under the conditions of homogenization,thus improving the dispersion stability of PHMX solutions.Therefore,under the premise of adding xanthan gum,HPH can better enhance the dispersion stability of the polypeptide in PHM.展开更多
By adopting sodium silicate as a major material,SiO_2 nanoparticles (size in 8-15nm) water-dispersiod was prepared by ion exchanging.The effects of sodium silicate concentration,surface-modifying time,temperature and ...By adopting sodium silicate as a major material,SiO_2 nanoparticles (size in 8-15nm) water-dispersiod was prepared by ion exchanging.The effects of sodium silicate concentration,surface-modifying time,temperature and technological conditions on their diameter,size distribution and dispersion stability were also studied.The result show that,the hydrophilic lipophlic and hydrophilic-lipophilic SiO_(2) nanoparticles water-dispersoid can be prepared through different kinds of surface-modifiers and the optimum reaction conditions have been determined as follows:sodium silicate solution concentration:8w%;silicone dosage:3% of the total mass of nano SiO_(2) water-dispersoid;adding way and time of surface-modifier:continual dropping for 2h;surface-modifying temperature:60-70℃.展开更多
Silicon dioxide sol was synthesized by silicon in the presence of alkali catalyst. SiO_2 nanoparticles (size in 8-15 nm) aqueous dispersion was prepared by using dispersion and surface modification in situ. The effect...Silicon dioxide sol was synthesized by silicon in the presence of alkali catalyst. SiO_2 nanoparticles (size in 8-15 nm) aqueous dispersion was prepared by using dispersion and surface modification in situ. The effects of reaction time, temperature, medium pH value, dispersant and surface-modifier on their diameters, sizes distribution and dispersion stability were also studied.The experimental results show that the preparation method can effectively resolve the dispersion stability of SiO_2 nanoparticles in water.展开更多
The conformation of polymers at the solid-liquid interface has been the subject of considerable interest in the fundamental theory and applied practice. In paints and printing inks, dispersions of pigment or filler po...The conformation of polymers at the solid-liquid interface has been the subject of considerable interest in the fundamental theory and applied practice. In paints and printing inks, dispersions of pigment or filler powders in polymeric binder solutions have to be maintained in the colloidal state. One of the stabilizing mechanisms for paint is the steric stabilization. On the other hand, in the formation reaction of polymer at the solid-liquid interface took place between monomer solutions and solid展开更多
ZrO2/PMMA nanocomposite particles are synthesized through an in-situ free radical emulsion polymerization based on the silane coupling agent （Z-6030） modified ZrO2 nanoparticles, and the morphology, size and its dis...ZrO2/PMMA nanocomposite particles are synthesized through an in-situ free radical emulsion polymerization based on the silane coupling agent （Z-6030） modified ZrO2 nanoparticles, and the morphology, size and its distribution of nanocomposite particles are investigated. Scanning electron microscopy （SEM） images demonstrate that the methyl methacrylate （MMA） feeding rate has a significant effect on the particle size and morphology. When the MMA feeding rate decreases from 0.42 ml-min-1 to 0.08 ml. min-1, large particles （about 200-550.nm） will not form, and the size distribution become narrow （36-54 nm）. The average nanocomposite particles size increases from 34 nm to 55 nm, as the MMA/ZrO2 nanoparticles mass ratio increased from 4 ： 1 to 16 ： 1. Regular spherical ZrO2/PMMA nanocomposite particles are synthesized when the emulsifier OP-10 concentration is 2 mg.m1-1. The nanocomposite particles could be mixed with VAc-VeoVa10 polymer matrix just by magnetic stirring to prepare the ZrOE/PMMA/VAc-VeoVal0 hybrid coatings. SEM and atomic force microscopy （AFM） photos reveal that the distribution of the ZrO2/PMMA nanocomposite particles in the VAc-VeoVal0 polymer matrix is homogenous and stable. Here, the grafted-PMMA polymer on ZrO2 nanoparticles plays as a bridge which effectively connects the ZrO2 nanoparticles and the VAc-VeoVal0 polymer matrix with improved comparability. In consequence, the hybrid coating with good dispersion stability is obtained.展开更多
Lanthanum hydroxide/graphene oxide nanocomposites(La(OH)3/GO)modified by octadecylamine(OCA),oleylamine(OLA),and polyvinylpyrrolidone(PVP)were prepared,respectively,as the base oil additives.The dispersion stability o...Lanthanum hydroxide/graphene oxide nanocomposites(La(OH)3/GO)modified by octadecylamine(OCA),oleylamine(OLA),and polyvinylpyrrolidone(PVP)were prepared,respectively,as the base oil additives.The dispersion stability of different modified La(OH)3/GO in base oil was studied by means of centrifugation.The tribological properties of oleophilic La(OH)3/GO in base oil were investigated using an UMT ball-disc tribometer.The micro-morphology and chemical composition of the worn surface were characterized by 3 D laser microscope,SEM,EDS,XPS,and Raman spectroscopy,respectively.The wettability performance of the worn surface was also studied based on the contact angle measurements.The test results showed that the OLA-La(OH)3/GO nanocomposites had good dispersion stability in base oil.The anti-wear performance of base oil was improved significantly by the addition of OLA-La(OH)3/GO nanocomposites.The characterizations of worn surface showed that the OLA-La(OH)3/GO nanocomposites could form the metal oxide and graphene protective films effectively on the friction interface and thus increased the oil wettability of the worn surface,thereby resulting in an improved wear resistance.展开更多
The target products were prepared by homogeneous precipitation method using SDS and PEG 800, respectively, as surfactant at a reaction temperature of 95 ℃ for 3 h, followed by calcination at 400 ~C for 3 h. The sampl...The target products were prepared by homogeneous precipitation method using SDS and PEG 800, respectively, as surfactant at a reaction temperature of 95 ℃ for 3 h, followed by calcination at 400 ~C for 3 h. The samples were charac- terized and analyzed by XRD, SEM, FTIR and zeta potential measurements. The products were modified with different sur- factants to improve their dispersion stability, both the amount and the best zeta potential values of which were identified in this work. The surface-modified nano-particles were added at a mass fraction of 1.0%, 2.0%, 3.0%, and 4.0%, respectively, into the base oil. It was showed that the additive in base oil has good oil solubility without detectable corrosion of copper stripe, and had excellent behavior in terms of anti-wear performance and lower friction coefficient.展开更多
Titanium dioxide(TiO_(2))nanocrystals have garnered significant interest in nanofluid research field due to their controllable morphology,eco-friendly nature,and superior lubrication properties.However,the long-term d...Titanium dioxide(TiO_(2))nanocrystals have garnered significant interest in nanofluid research field due to their controllable morphology,eco-friendly nature,and superior lubrication properties.However,the long-term dispersion stability of TiO_(2) nanocrystals remains a significant challenge.This study demonstrates that the morphology,{001}facet exposure,and consequent surface modifier adsorption density of TiO_(2) nanocrystals are synergistically controlled by modulating the facetspecific adsorption of oleic acid(OA),oleylamine(OM),and dioleamide during solvothermal synthesis.This control mechanism directly governs both dispersion stability and interfacial lubrication behavior.Crucially,the high-density modifier layer establishes a steric stabilization barrier,which ensures colloidal stability.The optimized TiO_(2) nanocrystals(TiO_(2)-OAOM)exhibit colloidal stability for over 5 months and enhance the antiwear properties of the base oil by 10-fold.Furthermore,synergistic interactions between TiO_(2)-OAOM and zinc dialkyl dithiophosphate(ZDDP)are confirmed in multiple friction pairs.These interactions promote the hardness and wear resistance of the tribo-film,thereby improving lubrication performance and suppressing metal transfer.This study provides a novel strategy for the co-optimization of dispersion stability and tribological properties of nanocrystals through surface engineering,offering novel insights into the design of nanofluids and a potent solution for lubrication challenges on lowhardness metals.展开更多
Nanocellulose,a natural polymeric nanomaterial,has attracted significant attention in enhanced oil recovery(EOR)applications due to its abundance,nanoscale,high oil-water interfacial adsorption ef-ficiency.In this stu...Nanocellulose,a natural polymeric nanomaterial,has attracted significant attention in enhanced oil recovery(EOR)applications due to its abundance,nanoscale,high oil-water interfacial adsorption ef-ficiency.In this study,surface-functionalized cellulose nanocrystals(SF-CNCs)were prepared via hy-drochloric acid hydrolysis and chemical modification,with adaptable nanosize and considerable dispersion stability in low-permeability reservoirs.The SF-CNCs were structurally characterized by FT-IR,Cryo-TEM,which have a diameter of 5-10 nm and a length of 100-200 nm.The SF-CNC dispersions possessed higher stability and stronger salt-tolerance than those of corresponding CNC dispersions,due to the strong hydrophilicity of the sulfonic acid group.It was synergistically used with a non-ionic surfactant(APG1214)to formulate a combined flooding system(0.1 wt%SF-CNC+0.2 wt%APG1214).The combined flooding system exhibits strong emulsification stability,low oil-water interfacial tension of o.03 mN/m,and the ability to alter the wettability for oil-wetting rocks.Furthermore,the combined system was_able to provide an optimum EOR efficiency of 20.2%in low-permeability cores with 30.13×10^(-3)μm^(2).Notably.it can enlarge the sweep volume and increase the displacement efficiency simultaneously.Overall,the newly formulated nanocellulose/surfactant combined system exhibits a remarkable EoR performance in low-permeability reservoirs.展开更多
In order to investigate the mechanism of nanoparticles enhancing the heat and mass transfer of the ammonia-water absorption process,several types of binary nanofluids were prepared by mixing Al2O3 nanoparticles with p...In order to investigate the mechanism of nanoparticles enhancing the heat and mass transfer of the ammonia-water absorption process,several types of binary nanofluids were prepared by mixing Al2O3 nanoparticles with polyacrylic acid(PAA),TiO2 with polyethylene glycol(PEG 1000),and TiN,SiC,hydroxyapatite(noodle-like) with PEG 10000 to ammonia-water solution,respectively.The thermal conductivities were measured by using a KD2 Pro thermal properties analyzer.The influences of surfactant and ammonia on the dispersion stabilities of the binary nanofluids were investigated by the light absorbency ratio index methods.The results show that the type,content and size of nanoparticles,the temperature as well as the dispersion stability are the key parameters that affect the thermal conductivity of nanofluids.For the given nanoparticle material and the base fluid,the thermal conductivity ratio of the nanofluid to the ammonia-water liquid increases as the nanoparticle content and the temperature are increased,and the diameter of nanoparticle is decreased.Furthermore,the thermal conductivity ratio increases significantly by improving the stabilities of nanofluids,which is achieved by adding surfactants or performing the proper ammonia content in the fluid.展开更多
Combined nitric acid oxidation method and polyaniline （PANI）-coated method were applied to modify the surface properties of short carbon fibers （SCF）. The electrical and mechanical properties of acrylic coatings w...Combined nitric acid oxidation method and polyaniline （PANI）-coated method were applied to modify the surface properties of short carbon fibers （SCF）. The electrical and mechanical properties of acrylic coatings with 50 wt pct PANI-coated carbon fiber were investigated by using scanning electron microscope （SEM）, UV-Vis spectrophotometer, four-probe method and the coaxial cable method. The results of the pH measurement and XPS （X-ray photoelectron spectroscopy） patterns showed that the oxygen functional groups, such as -OH and -COOH, were attached on the carbon fiber surfaces after oxidation treatment. The XPS analysis of PANl-coated oxidized SCF （PAOSCF） revealed that PANI may bond on the surface of oxidized SCF with chemical bonds. SEM images and surface roughness analyses showed that PANl-coated layer changed the surface morphology. Compared with SCF/acrylic coating, the surface resistivity of PAOSCF/acrylic coating decreased from17.1 to 5.3 Ω/sq and the shielding efficiency （SE） value increased from 1.54 to 23.3 dB.展开更多
By using self-made metal-alkoxide yttrium isopropoxide as a sintering additive and disperser of whisker, the SiC whisker reinforced AIN ceramics was prepared. Its apparent density is 99.5 percent of the theoretical de...By using self-made metal-alkoxide yttrium isopropoxide as a sintering additive and disperser of whisker, the SiC whisker reinforced AIN ceramics was prepared. Its apparent density is 99.5 percent of the theoretical density; its flexural strength and fracture toughness are 681 MPa and 5.21 MPa·m1/2 respectively. Comparing the result with that by applying Y2O3 powder as a sintering additive, the flexural strength is increased by 25% and the fracture toughness is increased by 33% . The dispersity of whisker by increased yttrium isopropoxide is significantly better than that by Triton X-100.展开更多
Partially deacetylated chitin nano-fiber(DAChN)dispersions were prepared using mechanical treatment of partially deacetylated crab shellα-chitin under acidic conditions mediated by various protonic acids.The represen...Partially deacetylated chitin nano-fiber(DAChN)dispersions were prepared using mechanical treatment of partially deacetylated crab shellα-chitin under acidic conditions mediated by various protonic acids.The representative organic acids had a better efficiency in terms of mediating the nanofibrillation of chitin fibers in comparison to the inorganic acid(HCl).The DAChN dispersed in water at a pH of 3.5 mediated by gluconic acid exhibited the highest yield of nano-fibers(88.6%),followed by succinic,itaconic,and ascorbic acids with a nano-fiber yield of 79.9%,73.3%and 66.0%,respectively.The pH,conductivity,viscosity,and light transmittance of dispersions were assessed under different storage times.All of the tested DAChN dispersions were stable for at least 15 weeks at 4℃.展开更多
A new method to chemically modify the surface of nanosized-SiO2 was studied in this paper.Nanosized-SiO2 was grafted with hyperbranched poly(amin ester)through one-spot polycondensation between AB2 monomer and active ...A new method to chemically modify the surface of nanosized-SiO2 was studied in this paper.Nanosized-SiO2 was grafted with hyperbranched poly(amin ester)through one-spot polycondensation between AB2 monomer and active hydroxyl on silica surface in present of catalyst.Compared with the results of FTIR and TEM,it is found hyperbranched poly(amin ester)is successfully grafted on the surface of nanosized-SiO2 and the surface properties have been changed with an expected way.The results indicate that nanosized-SiO2 grafted with hyperbranched poly(amin ester)has better dispersion in the ethanol or chloroform than that unmodified.展开更多
Nano-SiO2 was modified using silane coupling agent （KH-550） and hyperbranched poly（amine-ester） respectively, and Poly（vinyl chloride） （PVC）/modified nano-SiO2 composites were made by melt-blending. The compos...Nano-SiO2 was modified using silane coupling agent （KH-550） and hyperbranched poly（amine-ester） respectively, and Poly（vinyl chloride） （PVC）/modified nano-SiO2 composites were made by melt-blending. The composites＇ structures andmechanical properties were characterized by transmission electron microscopy（TEM）, sanning electronic microscopy（SEM） and electronic universal testing machine. The results. show that nano-SiO2 grafted by hyperbranched poly （amine-ester） increases obviously in dispersion in PVC matrix, and mechanical properties of PVC are effectively improved. Moreover, it was found that mechanical properties of PVC/nano-SiO2 composites reach the best when weight percent of nano-SiO2 in PVC matrix is 1%. Compared with crude PVC, the tensile strength of hyperbranched poly （amine-ester） grafted nano-SiO2/ PVC composite increases by 24.68 % and its break elongation, flexural strength and impact strength increase by 15.73%, 4.07% and 1 841.84%, respectively. Moreover, the processing of the composites is improved.展开更多
The formation mechanism of intragranular ferrites with acicular morphology was discussed.The ferrites were characterized by scanning electron microscopy.The results showed that the ferrites had an acicular structure w...The formation mechanism of intragranular ferrites with acicular morphology was discussed.The ferrites were characterized by scanning electron microscopy.The results showed that the ferrites had an acicular structure with radial,symmetrical,and acicular laths,and that the inclusions were the nucleation sites of the intragranular acicular ferrites.Transmission electron microscopy（TEM）was used to characterize the inclusions.The results of TEM with energy dispersive spectroscopy and TEM-selected area electron diffraction indicated that the complex inclusions consisted of Ti-Al complex oxides and MnS.The jagged edges of the complex inclusions can be ascribed to the effects of the crystal structure.The stabilization energy U of the coordination polyhedron growth units varies with the type of connection according to the calculation results.A larger Ucorresponds to more stable growth units,which induces the preferentially oriented growth of inclusions,at which point acicular ferrites are formed.展开更多
Co-precipitation method was selected for the preparation of Ni/Al_2O_3, Ni/ZrO_2 and Ni/CeO_2 catalysts, and their performances in methanation were investigated in this study. The structure and surface properties of t...Co-precipitation method was selected for the preparation of Ni/Al_2O_3, Ni/ZrO_2 and Ni/CeO_2 catalysts, and their performances in methanation were investigated in this study. The structure and surface properties of these catalysts were characterized by BET, XRD, H_2-TPD, TEM and H_2-TPR. The results showed that the catalytic activity at low temperature followed the order: Ni/Al_2O_3>Ni/ZrO_2>Ni/CeO_2. Ni/Al_2O_3 catalyst presented the best catalytic performance with the highest CH_4 selectivity of 94.5%. The characterization results indicated that the dispersion of the active component Ni was the main factor affecting the catalytic activity and the one with higher dispersion gave better performance.展开更多
A new method of surface chemical modification of nano-SiO2 is proposed in this paper. In the presence of catalyst, the active hydroxyl groups on the surface of nano-SiO2 reacted with AB2-type monomer （N, N-dihydroxye...A new method of surface chemical modification of nano-SiO2 is proposed in this paper. In the presence of catalyst, the active hydroxyl groups on the surface of nano-SiO2 reacted with AB2-type monomer （N, N-dihydroxyethyl-3-amino methyl propionate） by one-step polycondensation. And the product＇s Fourer transform infrared （FTIR） graphs and transmission electron microscopy（TEM） images proved that hyperbranched poly （amine-ester） was grafted on nano-SiO2 surface successfully. Results show that the modified nano-SiO2 exhibits excellent dispersion and stability in some solvents such as alcohol and chloroform.展开更多
In order to prepare cellulose nanocrystals( CNCs)-coated polylactide( PLA) microspheres for the use of drug delivery and tissue engineering,a Pickering emulsion route was applied. The stable Pickering emulsions were p...In order to prepare cellulose nanocrystals( CNCs)-coated polylactide( PLA) microspheres for the use of drug delivery and tissue engineering,a Pickering emulsion route was applied. The stable Pickering emulsions were prepared using CNCs as efficient stabilizers without any additional surfactant. The microspheres were successfully fabricated after volatilization of the solvent. What's more,the size of microspheres could be controlled by fabrication parameters.展开更多
Liquid-phase exfoliation （LPE） is an attractive method for the scaling-up of exfoliated MoS2 sheets compared to chemical vapor deposition and mechanical cleavage. However, the MoS2 nanosheet yield from LPE is too sm...Liquid-phase exfoliation （LPE） is an attractive method for the scaling-up of exfoliated MoS2 sheets compared to chemical vapor deposition and mechanical cleavage. However, the MoS2 nanosheet yield from LPE is too small for practical applications. We report a facile method for the scaling-up of exfoliated MoS2 nanosheets using freeze-dried silk fibroin powders. Compared to MoS2 dispersion in the absence of silk fibroin powder, sonicated MoS2 dispersions with silk fibroin powder （MoSJSilk dispersion） show noticeably higher exfoliated MoS2 nanosheet yields, with suspended MoS2 concentrations in MoS2/Silk dispersions sonicated for 2 and 5 h of 1.03 and 1.39 mg.mL-1, respectively. The MoS2 concentration in the MoS2/Silk dispersion after centrifugation above 10,000 rpm is more than four times that without the silk fibroin. The size of the dispersed silk fibroin is controlled by the change of centrifugation rate, showing the removal of silk fibroin above tens of micrometers in size after centrifugation at 2,000 rpm. Size-controlled silk fibroin biomolecules combined with MoS2 nanosheets are expected to increase the practical use of such materials in fields related to tissue engineering, biosensors and electrochemical electrodes. Atomic force microscopy and Raman spectroscopy provide the height of the MoS2 nanosheets spin-cast from MoS2/Silk dispersions, showing thicknesses of 3--6 nm. X-ray photoelectron spectroscopy and X-ray diffraction indicate that the outermost surface layer of the hydrophobic MoS2 crystals interact with oxygen-containing functional groups that exist in the hydrophobic part of silk fibroins. The amphiphilic properties of silk fibroin combined with the MoS2 nanosheets stabilize dispersions by enhancing solvent-material interactions. The large quantities of exfoliated MoS2 nanosheets suspended in the as-synthesized dispersions can be utilized for the fabrication of vapor and electrochemical devices requiring high MoS2 nanosheets contents.展开更多
基金This work was supported by the State Key Research and Development Plan M¨odern Food Processing and Food Storage and Transportation Technology and Equipment”(2017YFD0400201)by the National Natural Science Foundation of China(31771926).
文摘Owing to the formation of aggregation and gelation during storage,certain proteins and peptides exhibit limited applications in aqueous protein food products.The purpose of this study was to investigate the influence of homogenization and xanthan gum addition on the dispersion stability of Mytilus edulis hydrolysate(PHM).High-pressure homogenization(HPH)at 360 and 40 bar in the first and second values,respectively,and adding xanthan gum at a concentration of 1 mg/mL showed significantly improvement on the stability of the PHM solution.PHM-xanthan gum solutions(PHMX)showed the highest polypeptide precipitation rate and turbidity retention rate compared with those of PHM.Moreover,the centrifugal precipitation rate of PHMX without HPH was higher than that of homogeneous PHMX.After HPH treatment at 400 bar,the percentage of smaller particles in PHM and PHMX was increased,the aqueous system became more uniform,and the fluorescence intensity reached its maximum.HPH pretreatment improved the polypeptide dispersion stability and turbidity retention rate of PHM and PHMX and reduced the fluorescence intensity.The interactions of xanthan gum and polypeptide render the network microstructure more uniform under the conditions of homogenization,thus improving the dispersion stability of PHMX solutions.Therefore,under the premise of adding xanthan gum,HPH can better enhance the dispersion stability of the polypeptide in PHM.
文摘By adopting sodium silicate as a major material,SiO_2 nanoparticles (size in 8-15nm) water-dispersiod was prepared by ion exchanging.The effects of sodium silicate concentration,surface-modifying time,temperature and technological conditions on their diameter,size distribution and dispersion stability were also studied.The result show that,the hydrophilic lipophlic and hydrophilic-lipophilic SiO_(2) nanoparticles water-dispersoid can be prepared through different kinds of surface-modifiers and the optimum reaction conditions have been determined as follows:sodium silicate solution concentration:8w%;silicone dosage:3% of the total mass of nano SiO_(2) water-dispersoid;adding way and time of surface-modifier:continual dropping for 2h;surface-modifying temperature:60-70℃.
文摘Silicon dioxide sol was synthesized by silicon in the presence of alkali catalyst. SiO_2 nanoparticles (size in 8-15 nm) aqueous dispersion was prepared by using dispersion and surface modification in situ. The effects of reaction time, temperature, medium pH value, dispersant and surface-modifier on their diameters, sizes distribution and dispersion stability were also studied.The experimental results show that the preparation method can effectively resolve the dispersion stability of SiO_2 nanoparticles in water.
文摘The conformation of polymers at the solid-liquid interface has been the subject of considerable interest in the fundamental theory and applied practice. In paints and printing inks, dispersions of pigment or filler powders in polymeric binder solutions have to be maintained in the colloidal state. One of the stabilizing mechanisms for paint is the steric stabilization. On the other hand, in the formation reaction of polymer at the solid-liquid interface took place between monomer solutions and solid
基金Supported by Production, Teaching & Research Combination Project for Universities in Guangdong Province(cgzhzd0904),Department of Education of Guangdong Province, China
文摘ZrO2/PMMA nanocomposite particles are synthesized through an in-situ free radical emulsion polymerization based on the silane coupling agent （Z-6030） modified ZrO2 nanoparticles, and the morphology, size and its distribution of nanocomposite particles are investigated. Scanning electron microscopy （SEM） images demonstrate that the methyl methacrylate （MMA） feeding rate has a significant effect on the particle size and morphology. When the MMA feeding rate decreases from 0.42 ml-min-1 to 0.08 ml. min-1, large particles （about 200-550.nm） will not form, and the size distribution become narrow （36-54 nm）. The average nanocomposite particles size increases from 34 nm to 55 nm, as the MMA/ZrO2 nanoparticles mass ratio increased from 4 ： 1 to 16 ： 1. Regular spherical ZrO2/PMMA nanocomposite particles are synthesized when the emulsifier OP-10 concentration is 2 mg.m1-1. The nanocomposite particles could be mixed with VAc-VeoVa10 polymer matrix just by magnetic stirring to prepare the ZrOE/PMMA/VAc-VeoVal0 hybrid coatings. SEM and atomic force microscopy （AFM） photos reveal that the distribution of the ZrO2/PMMA nanocomposite particles in the VAc-VeoVal0 polymer matrix is homogenous and stable. Here, the grafted-PMMA polymer on ZrO2 nanoparticles plays as a bridge which effectively connects the ZrO2 nanoparticles and the VAc-VeoVal0 polymer matrix with improved comparability. In consequence, the hybrid coating with good dispersion stability is obtained.
基金supported by the National Natural Science Foundation of China(Grant No.51675153)。
文摘Lanthanum hydroxide/graphene oxide nanocomposites(La(OH)3/GO)modified by octadecylamine(OCA),oleylamine(OLA),and polyvinylpyrrolidone(PVP)were prepared,respectively,as the base oil additives.The dispersion stability of different modified La(OH)3/GO in base oil was studied by means of centrifugation.The tribological properties of oleophilic La(OH)3/GO in base oil were investigated using an UMT ball-disc tribometer.The micro-morphology and chemical composition of the worn surface were characterized by 3 D laser microscope,SEM,EDS,XPS,and Raman spectroscopy,respectively.The wettability performance of the worn surface was also studied based on the contact angle measurements.The test results showed that the OLA-La(OH)3/GO nanocomposites had good dispersion stability in base oil.The anti-wear performance of base oil was improved significantly by the addition of OLA-La(OH)3/GO nanocomposites.The characterizations of worn surface showed that the OLA-La(OH)3/GO nanocomposites could form the metal oxide and graphene protective films effectively on the friction interface and thus increased the oil wettability of the worn surface,thereby resulting in an improved wear resistance.
基金supported by the Liaoning Provincial Office of Education for Innovation Team (2006T001)Liaoning Province of Key Laboratory Project (2008403001)
文摘The target products were prepared by homogeneous precipitation method using SDS and PEG 800, respectively, as surfactant at a reaction temperature of 95 ℃ for 3 h, followed by calcination at 400 ~C for 3 h. The samples were charac- terized and analyzed by XRD, SEM, FTIR and zeta potential measurements. The products were modified with different sur- factants to improve their dispersion stability, both the amount and the best zeta potential values of which were identified in this work. The surface-modified nano-particles were added at a mass fraction of 1.0%, 2.0%, 3.0%, and 4.0%, respectively, into the base oil. It was showed that the additive in base oil has good oil solubility without detectable corrosion of copper stripe, and had excellent behavior in terms of anti-wear performance and lower friction coefficient.
基金supported by Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB0470202)International Partnership Program of Chinese Academy of Sciences(No.307GJHZ2022034GC)Key Project of the Henan Province Science and Technology Research and Development Joint Funds(No.235101610007).
文摘Titanium dioxide(TiO_(2))nanocrystals have garnered significant interest in nanofluid research field due to their controllable morphology,eco-friendly nature,and superior lubrication properties.However,the long-term dispersion stability of TiO_(2) nanocrystals remains a significant challenge.This study demonstrates that the morphology,{001}facet exposure,and consequent surface modifier adsorption density of TiO_(2) nanocrystals are synergistically controlled by modulating the facetspecific adsorption of oleic acid(OA),oleylamine(OM),and dioleamide during solvothermal synthesis.This control mechanism directly governs both dispersion stability and interfacial lubrication behavior.Crucially,the high-density modifier layer establishes a steric stabilization barrier,which ensures colloidal stability.The optimized TiO_(2) nanocrystals(TiO_(2)-OAOM)exhibit colloidal stability for over 5 months and enhance the antiwear properties of the base oil by 10-fold.Furthermore,synergistic interactions between TiO_(2)-OAOM and zinc dialkyl dithiophosphate(ZDDP)are confirmed in multiple friction pairs.These interactions promote the hardness and wear resistance of the tribo-film,thereby improving lubrication performance and suppressing metal transfer.This study provides a novel strategy for the co-optimization of dispersion stability and tribological properties of nanocrystals through surface engineering,offering novel insights into the design of nanofluids and a potent solution for lubrication challenges on lowhardness metals.
基金the China National Postdoctoral Program for Innovative Talents(Bx20200386)China Postdoctoral Science Foundation(2021M703586)+1 种基金Key Program of National Natural Science Foundation of China(52130401)National Natural Science Foundation of China(52204064,52104055)for financial support.
文摘Nanocellulose,a natural polymeric nanomaterial,has attracted significant attention in enhanced oil recovery(EOR)applications due to its abundance,nanoscale,high oil-water interfacial adsorption ef-ficiency.In this study,surface-functionalized cellulose nanocrystals(SF-CNCs)were prepared via hy-drochloric acid hydrolysis and chemical modification,with adaptable nanosize and considerable dispersion stability in low-permeability reservoirs.The SF-CNCs were structurally characterized by FT-IR,Cryo-TEM,which have a diameter of 5-10 nm and a length of 100-200 nm.The SF-CNC dispersions possessed higher stability and stronger salt-tolerance than those of corresponding CNC dispersions,due to the strong hydrophilicity of the sulfonic acid group.It was synergistically used with a non-ionic surfactant(APG1214)to formulate a combined flooding system(0.1 wt%SF-CNC+0.2 wt%APG1214).The combined flooding system exhibits strong emulsification stability,low oil-water interfacial tension of o.03 mN/m,and the ability to alter the wettability for oil-wetting rocks.Furthermore,the combined system was_able to provide an optimum EOR efficiency of 20.2%in low-permeability cores with 30.13×10^(-3)μm^(2).Notably.it can enlarge the sweep volume and increase the displacement efficiency simultaneously.Overall,the newly formulated nanocellulose/surfactant combined system exhibits a remarkable EoR performance in low-permeability reservoirs.
基金Projects(51176029,50876020) supported by the National Natural Science Foundation of ChinaProject(2011BAJ03B00) supported by the 12th Five-Year National Science and Technology Support Key Program of China Project(ybjj1124) supported by the Foundation of Graduate School of Southeast University,China
文摘In order to investigate the mechanism of nanoparticles enhancing the heat and mass transfer of the ammonia-water absorption process,several types of binary nanofluids were prepared by mixing Al2O3 nanoparticles with polyacrylic acid(PAA),TiO2 with polyethylene glycol(PEG 1000),and TiN,SiC,hydroxyapatite(noodle-like) with PEG 10000 to ammonia-water solution,respectively.The thermal conductivities were measured by using a KD2 Pro thermal properties analyzer.The influences of surfactant and ammonia on the dispersion stabilities of the binary nanofluids were investigated by the light absorbency ratio index methods.The results show that the type,content and size of nanoparticles,the temperature as well as the dispersion stability are the key parameters that affect the thermal conductivity of nanofluids.For the given nanoparticle material and the base fluid,the thermal conductivity ratio of the nanofluid to the ammonia-water liquid increases as the nanoparticle content and the temperature are increased,and the diameter of nanoparticle is decreased.Furthermore,the thermal conductivity ratio increases significantly by improving the stabilities of nanofluids,which is achieved by adding surfactants or performing the proper ammonia content in the fluid.
文摘Combined nitric acid oxidation method and polyaniline （PANI）-coated method were applied to modify the surface properties of short carbon fibers （SCF）. The electrical and mechanical properties of acrylic coatings with 50 wt pct PANI-coated carbon fiber were investigated by using scanning electron microscope （SEM）, UV-Vis spectrophotometer, four-probe method and the coaxial cable method. The results of the pH measurement and XPS （X-ray photoelectron spectroscopy） patterns showed that the oxygen functional groups, such as -OH and -COOH, were attached on the carbon fiber surfaces after oxidation treatment. The XPS analysis of PANl-coated oxidized SCF （PAOSCF） revealed that PANI may bond on the surface of oxidized SCF with chemical bonds. SEM images and surface roughness analyses showed that PANl-coated layer changed the surface morphology. Compared with SCF/acrylic coating, the surface resistivity of PAOSCF/acrylic coating decreased from17.1 to 5.3 Ω/sq and the shielding efficiency （SE） value increased from 1.54 to 23.3 dB.
文摘By using self-made metal-alkoxide yttrium isopropoxide as a sintering additive and disperser of whisker, the SiC whisker reinforced AIN ceramics was prepared. Its apparent density is 99.5 percent of the theoretical density; its flexural strength and fracture toughness are 681 MPa and 5.21 MPa·m1/2 respectively. Comparing the result with that by applying Y2O3 powder as a sintering additive, the flexural strength is increased by 25% and the fracture toughness is increased by 33% . The dispersity of whisker by increased yttrium isopropoxide is significantly better than that by Triton X-100.
基金supported by the National Forestry Public Welfare Industry Research Project (201304609)the National Natural Science Foundation of China (31100426)Specialized Research Fund for the Doctoral Program of Higher Education of China (20133204110008).
文摘Partially deacetylated chitin nano-fiber(DAChN)dispersions were prepared using mechanical treatment of partially deacetylated crab shellα-chitin under acidic conditions mediated by various protonic acids.The representative organic acids had a better efficiency in terms of mediating the nanofibrillation of chitin fibers in comparison to the inorganic acid(HCl).The DAChN dispersed in water at a pH of 3.5 mediated by gluconic acid exhibited the highest yield of nano-fibers(88.6%),followed by succinic,itaconic,and ascorbic acids with a nano-fiber yield of 79.9%,73.3%and 66.0%,respectively.The pH,conductivity,viscosity,and light transmittance of dispersions were assessed under different storage times.All of the tested DAChN dispersions were stable for at least 15 weeks at 4℃.
文摘A new method to chemically modify the surface of nanosized-SiO2 was studied in this paper.Nanosized-SiO2 was grafted with hyperbranched poly(amin ester)through one-spot polycondensation between AB2 monomer and active hydroxyl on silica surface in present of catalyst.Compared with the results of FTIR and TEM,it is found hyperbranched poly(amin ester)is successfully grafted on the surface of nanosized-SiO2 and the surface properties have been changed with an expected way.The results indicate that nanosized-SiO2 grafted with hyperbranched poly(amin ester)has better dispersion in the ethanol or chloroform than that unmodified.
基金Sponsored by the Ministerial Level Advanced Research Foundation (120701BQ0126)
文摘Nano-SiO2 was modified using silane coupling agent （KH-550） and hyperbranched poly（amine-ester） respectively, and Poly（vinyl chloride） （PVC）/modified nano-SiO2 composites were made by melt-blending. The composites＇ structures andmechanical properties were characterized by transmission electron microscopy（TEM）, sanning electronic microscopy（SEM） and electronic universal testing machine. The results. show that nano-SiO2 grafted by hyperbranched poly （amine-ester） increases obviously in dispersion in PVC matrix, and mechanical properties of PVC are effectively improved. Moreover, it was found that mechanical properties of PVC/nano-SiO2 composites reach the best when weight percent of nano-SiO2 in PVC matrix is 1%. Compared with crude PVC, the tensile strength of hyperbranched poly （amine-ester） grafted nano-SiO2/ PVC composite increases by 24.68 % and its break elongation, flexural strength and impact strength increase by 15.73%, 4.07% and 1 841.84%, respectively. Moreover, the processing of the composites is improved.
基金Item Sponsored by National Natural Science Foundation of China(51574106,51474089)Key Funds of Natural Science Foundation of Hebei Province of China(E2016209396)+1 种基金Natural Science Foundation of Hebei Province of China(E2013209207)Research Science Institute on High-level Personnel of Colleges in Hebei Province of China(GCC20142030)
文摘The formation mechanism of intragranular ferrites with acicular morphology was discussed.The ferrites were characterized by scanning electron microscopy.The results showed that the ferrites had an acicular structure with radial,symmetrical,and acicular laths,and that the inclusions were the nucleation sites of the intragranular acicular ferrites.Transmission electron microscopy（TEM）was used to characterize the inclusions.The results of TEM with energy dispersive spectroscopy and TEM-selected area electron diffraction indicated that the complex inclusions consisted of Ti-Al complex oxides and MnS.The jagged edges of the complex inclusions can be ascribed to the effects of the crystal structure.The stabilization energy U of the coordination polyhedron growth units varies with the type of connection according to the calculation results.A larger Ucorresponds to more stable growth units,which induces the preferentially oriented growth of inclusions,at which point acicular ferrites are formed.
基金financial support from the National Science and Technology Supporting Plan through contract (2015BAD15B06)the National Natural Science Foundation of China (51661145011)
文摘Co-precipitation method was selected for the preparation of Ni/Al_2O_3, Ni/ZrO_2 and Ni/CeO_2 catalysts, and their performances in methanation were investigated in this study. The structure and surface properties of these catalysts were characterized by BET, XRD, H_2-TPD, TEM and H_2-TPR. The results showed that the catalytic activity at low temperature followed the order: Ni/Al_2O_3>Ni/ZrO_2>Ni/CeO_2. Ni/Al_2O_3 catalyst presented the best catalytic performance with the highest CH_4 selectivity of 94.5%. The characterization results indicated that the dispersion of the active component Ni was the main factor affecting the catalytic activity and the one with higher dispersion gave better performance.
基金Sponsored by the Ministerial Level Advanced Research Foundation (120701BQ0126)
文摘A new method of surface chemical modification of nano-SiO2 is proposed in this paper. In the presence of catalyst, the active hydroxyl groups on the surface of nano-SiO2 reacted with AB2-type monomer （N, N-dihydroxyethyl-3-amino methyl propionate） by one-step polycondensation. And the product＇s Fourer transform infrared （FTIR） graphs and transmission electron microscopy（TEM） images proved that hyperbranched poly （amine-ester） was grafted on nano-SiO2 surface successfully. Results show that the modified nano-SiO2 exhibits excellent dispersion and stability in some solvents such as alcohol and chloroform.
基金National Key Technology R&D Program of China(No.2014BAC13B02)National Natural Science Foundation of China(No.51403035)+1 种基金Programme of Introducing Talents of Discipline to Universities,China(No.105-07-005735)the Fundamental Research Funds for the Central Universities,China(No.15D110510)
文摘In order to prepare cellulose nanocrystals( CNCs)-coated polylactide( PLA) microspheres for the use of drug delivery and tissue engineering,a Pickering emulsion route was applied. The stable Pickering emulsions were prepared using CNCs as efficient stabilizers without any additional surfactant. The microspheres were successfully fabricated after volatilization of the solvent. What's more,the size of microspheres could be controlled by fabrication parameters.
文摘Liquid-phase exfoliation （LPE） is an attractive method for the scaling-up of exfoliated MoS2 sheets compared to chemical vapor deposition and mechanical cleavage. However, the MoS2 nanosheet yield from LPE is too small for practical applications. We report a facile method for the scaling-up of exfoliated MoS2 nanosheets using freeze-dried silk fibroin powders. Compared to MoS2 dispersion in the absence of silk fibroin powder, sonicated MoS2 dispersions with silk fibroin powder （MoSJSilk dispersion） show noticeably higher exfoliated MoS2 nanosheet yields, with suspended MoS2 concentrations in MoS2/Silk dispersions sonicated for 2 and 5 h of 1.03 and 1.39 mg.mL-1, respectively. The MoS2 concentration in the MoS2/Silk dispersion after centrifugation above 10,000 rpm is more than four times that without the silk fibroin. The size of the dispersed silk fibroin is controlled by the change of centrifugation rate, showing the removal of silk fibroin above tens of micrometers in size after centrifugation at 2,000 rpm. Size-controlled silk fibroin biomolecules combined with MoS2 nanosheets are expected to increase the practical use of such materials in fields related to tissue engineering, biosensors and electrochemical electrodes. Atomic force microscopy and Raman spectroscopy provide the height of the MoS2 nanosheets spin-cast from MoS2/Silk dispersions, showing thicknesses of 3--6 nm. X-ray photoelectron spectroscopy and X-ray diffraction indicate that the outermost surface layer of the hydrophobic MoS2 crystals interact with oxygen-containing functional groups that exist in the hydrophobic part of silk fibroins. The amphiphilic properties of silk fibroin combined with the MoS2 nanosheets stabilize dispersions by enhancing solvent-material interactions. The large quantities of exfoliated MoS2 nanosheets suspended in the as-synthesized dispersions can be utilized for the fabrication of vapor and electrochemical devices requiring high MoS2 nanosheets contents.
