12874 results about "Centrifugal separation" patented technology

A multi cyclone vessel dust collecting apparatus comprises a first cyclone vessel for centrifugally separating contaminants from drawn in air; a plurality of a second cyclone vessels configured on the first cyclone vessel; and a contaminant collecting unit attached to a bottom portion of the first cyclone vessel. Each of a plurality of the second cyclone vessels are parallel to each other. The center axis line of air rotation movement of the second cyclone vessel is substantially perpendicular to that of the first cyclone vessel. The contaminants collecting unit comprises a body which can be used as a handle.

The PRP separator-concentrator of this invention is suitable for office use or emergency use for trauma victims. The PRP separator comprises a motorized centrifugal separation assembly, and a concentrator assembly. The centrifugal separator assembly comprises a centrifugal drum separator that includes an erythrocyte capture module and a motor having a drive axis connected to the centrifugal drum separator. The concentrator assembly comprises a water-removal module for preparing PRP concentrate. The centrifugal drum separator has an erythrocyte trap. The water removal module can be a syringe device with water absorbing beads or it can be a pump-hollow fiber cartridge assembly. The hollow fibers are membranes with pores that allow the flow of water through the fiber membrane while excluding flow of clotting factors useful for sealing and adhering tissue and growth factors helpful for healing while avoiding activation of platelets and disruption of any trace erythrocytes present in the PRP.

The invention discloses a method for producing humic acid and salt thereof through the oxidative degradation of young lignite. The method comprises the following steps: carrying out the oxidation reaction of the lignite containing the humic acid and aqueous hydrogen peroxide solution; after the reaction, obtaining water soluble fulvic acid through centrifugal separation, supernatant filtration, concentration and drying; adding alkali into the fulvic acid to prepare a fulvic acid salt product; carrying out the alkaline extraction and centrifugal separation of the residue deposit of the production of the fulvic acid, adding acid into the supernatant till the pH value is 1 to 2, carrying out a reaction at an increased temperature or room temperature, carrying out centrifugal separation after the reaction is finished, and obtaining purified ulmic acid after precipitation and drying; and directly concentrating and drying the supernatant in the previous step to obtain the humate. The method can improve the yield of the fulvic acid and total humic acid in the young lignite, and simultaneously increase the active group in the humic acid. The method can be used for producing fulvic acid, fulvic acid salt, ulmic acid and ulmic acid salt products. In particular, the method puts an end to the environmental pollution caused by the nitric acid which is taken as an oxidation degradation agent. In addition, the method has a short technological line, low cost, simple requirements on equipment, and moderate conditions. The method which can be applied to the industrialized production has good application prospect.

The PRP separator-concentrator of this invention is suitable for office use or emergency use for trauma victims. The PRP separator comprises a motorized centrifugal separation assembly, and a concentrator assembly. The centrifugal separator assembly comprises a centrifugal drum separator that includes an erythrocyte capture module and a motor having a drive axis connected to the centrifugal drum separator. The concentrator assembly comprises a water-removal module for preparing PRP concentrate. The centrifugal drum separator has an erythrocyte trap. The water removal module can be a syringe device with water absorbing beads or it can be a pump-hollow fiber cartridge assembly. The hollow fibers are membranes with pores that allow the flow of water through the fiber membrane while excluding flow of clotting factors useful for sealing and adhering tissue and growth factors helpful for healing while avoiding activation of platelets and disruption of any trace erythrocytes present in the PRP.

A separator disk (4) for use in centrifugal separation of components is designed to automatically position itself during separation at the interface between the supernatant and the remaining components. Preferably the interface is between plasma and red blood cells.

A Plasma or serum separation membrane that enables omitting centrifugal separation, is free from hemolysis attributed to destruction of red blood cells and realizes easy and rapid separation of plasma or serum from blood; and a filter apparatus including the plasma or serum separation membrane. In particular, a plasma or serum separation membrane being a membrane for separation of plasma or serum from blood and having a void ratio of 30% or below; and a filter apparatus comprising a filter member capable of attaining movement of plasma swifter than movement of blood cells and a plasma or serum separation membrane connected in series with a rear side of the filter member.

A method and apparatus is described by which means molecules in suspension may be characterized in terms of the size and mass distributions present. As a sample solution is separated by centrifugal means, it is illuminated at a particular radial distance from the axis of rotation by a fine, preferably monochromatic, light beam. Despite the high resolution of such devices, a key problem associated with most separators based upon use of centrifugal forces is the difficulty in deriving the absolute size and / or molar mass of the separating molecules. By integrating means to detect light scattered, over a range of scattering angles, from samples undergoing centrifugal separation, molecular sizes in the sub-micrometer range may be derived, even in the presence of diffusion. Adding a second light beam at a displaced rotational angle, preferably of an ultraviolet wavelength, that intersects the sample at the same radial region as the first beam permits determination of the molecular concentration at that region. Combining the light scattering data with the associated concentration permits the determination of the associated molar mass. In a preferred embodiment, the light beam and detectors may be controlled to scan synchronously the sample radially during separation.

The invention relates to a method for producing copper chloride hydroxide and blue vitriod by using cupriferous etching wastewater; the method comprises the following steps: acidic copper chloride etching wastewater and alkaline copper chloride etching wastewater are neutralized and crystallized to get acidic copper chloride crystal under the condition of strictly controlling filling liquid and the Ph range of a reaction kettle, and then pumped and filtrated, and centrifugated; part of the obtained alkaline copper chloride crystal is dried to obtain finished products while the other is added with NaOH solution for alkali conversion to obtain copper oxide, and then is acidulated by sulphuric acid, crystallized, washed, centrifugated, and dried to obtain blue vitriod products. The method for producing blue vitriod by directly using sulphuric acid-oxyful etching wastewater includes the following steps: sulphuric acid-oxyful etching wastewater and composition brass wasterwater in a PCB manufacture are blended together and added with NaOH to form cupric hydroxide precipitation which filtrated, washed, and then acidulated by sulphuric acid to obtain copper sulphate solution; after the copper sulphate solution is cooled, crystallized, centrifugated and dried, and the blue vitriod is obtained.

The invention discloses a quick and efficient synthesis method for silver nanowires. The method comprises the following steps of: 1) introducing inert gas into a reactor, adding 2 volume parts of glycol into the reactor, and stirring, heating, condensing and refluxing the glycol; quickly adding 1 volume part of glycol solution of silver nitrate at molar concentration of between 0.1 and 0.5m into the reactor; slowly dropwise adding 1 to 2 volume parts of PVP at molar concentration of between 0.15 and 0.75m and 4 to 32 mu m of glycol solution of MnCl2 at the same time; and reacting and cooling the mixture to the room temperature to obtain reaction mother liquor of the silver nanowires; and 2) transferring the reaction mother liquor of the silver nanowires into a centrifugal tube; adding acetone into the centrifugal tube and performing centrifugal separation to remove supernatant and retain precipitate; adding de-ionized water or ethanol into the centrifugal tube and performing centrifugal separation to remove the supernatant and retain precipitate, and repeating the operation for 1 to 3 times; and extracting and dispersing the precipitate with ethanol to obtain the silver nanowires. The method shortens the reaction time and also has high selectivity for the synthesis of the silver nanowires under conditions of high concentration.

The weight difference is limited between buckets (17) mounted at respective symmetrical positions with respect to a centrifugal separation rotational center and examination of samples is continuously performed in the order in which they are received. In particular, when a sample (21) is carried in a centrifugal buffer line (11), its weight is measured by weight measuring means (31). It is assumed that the names of two adaptors (22) placed at respective symmetrical positions with respect to the centrifugal separation rotational center are defined as an adaptor A and an adaptor B. A first sample is put on the adaptor A and a second sample is put on the adaptor B. Then, a third sample and subsequent ones are each put on the adaptor (22) lighter than the other adaptor after the total weights of samples put on the adaptors are computation-compared with each other.

The invention provides an oily sludge recycling and innocent comprehensive treatment process, which comprises the following four steps of: 1, pretreating oily sludge: adding water into the oil sludge, heating and stirring to form fluidized sludge, and separating in a stainless steel screen; 2, conditioning the oily sludge, adding a demulsifier and a flocculant into the separated fluidized sludge for conditioning the oily sludge; 3, performing centrifugal separation on three phases of the oily sludge: introducing separated oil into an oil-water separation system for recovering crude oil, conveying separated water to the oily sludge pretreatment step for recycling, drying the separated residual oily sludge, and solid impurities and floating slag which are separated in the oily sludge pretreatment, and introducing the dried substances into a rotary kiln incinerator; and 4, performing mixed combustion on the residual oily sludge and biomass, performing high temperature incineration treatment after the residual oily sludge, the separated solid impurities and floating slag, and the biomass are mixed in a rotary kiln to remove the secondary pollution of the oily sludge, and recovering afterheat from high temperature flue gas.

The invention provides a preparation method of dispersible silane functionalized graphene. The method comprises the steps of: conducting ultrasonic dispersion to graphene oxide in absolute ethyl alcohol so as to form a uniform graphene oxide dispersion solution, then adjusting the pH value to 3-4, or under the protection of an inert atmosphere, adding silane into the dispersing solution for modification, with silane and graphene oxide in a mass ratio of 0.1:1-5:1, continuing the reaction for 12h-48h at a temperature ranging from normal temperature to 78DEG C, carrying out centrifugation, then adding hydrazine hydrate to the obtained solid, performing heating reduction, and filtering the reaction solution, then washing and drying the filter cake, thus obtaining dispersible silane functionalized grapheme. The method of the invention is simple and practicable, and the obtained silane functionalized grapheme has good dispersibility in solvents like absolute ethyl alcohol, acetone, toluene, ethyl acetate, butyl acetate, and tetrahydrofuran (THF), etc.

The invention relates to a method for removing heavy metal ions in water by using a graphene oxide sheet, which belongs to the technical fields of water purification and environmental protection. In the invention, the graphene oxide sheet is used as an adsorbent of the heavy metal ions, wherein the graphene oxide sheet is of a monatomic layer two-dimensional structure and has a huge specific surface while ensuring no obvious toxicity. In the purification process of the method, the operations are simple without pollution, and the copper ion adsorption efficiency is 10 times that of the active carbon. In the invention, the graphene oxide sheet adsorbing the metal ions can be recovered to the single sheet structure by a centrifugal separation or dialysis method and can be recycled.

An apparatus and method are provided for separating components of a fluid or particles. A separation vessel having a barrier dam is provided to initially separate an intermediate density components of a fluid, and a fluid chamber is provided to further separate these intermediate density components by forming an elutriative field or saturated fluidized particle bed. The separation vessel includes a shield for limiting flow into the fluid chamber of relatively high density substances, such as red blood cells. The separation vessel also includes a trap dam with a smooth, gradually sloped downstream section for reducing mixing of substances. Structure is also provided for adding additional plasma to platelets and plasma flowing from the fluid chamber. The system reduces clumping of platelets by limiting contact between the platelets and walls of the separation vessel.

Cleaning assemblies and particulate tolerant fluid bearings that are particularly well suited for use in centrifugal separation enhanced filtration devices are described. In one aspect of the invention, at least one bearing is arranged to carry a circulating cleaning assembly such that the cleaning assembly can rotate around a filter membrane during filtering operation of the filtration device. The bearing is preferably arranged to maintain the circulating cleaning assembly in a substantially coaxial alignment with the filter membrane and in a substantially stable longitudinal position relative to the filter membrane as the circulating cleaning assembly is rotated around the filter membrane. In another aspect of the invention a variety of particulate tolerant bearings are described.

A method has been invented for separating components of a wastewater stream, the stream containing water, oil (e.g. heavy oil and / or light oil), undesirable organic material (solid and / or liquid), and contaminating solids, the method including feeding a wastewater stream to a first pre-treatment unit producing a first pretreated stream, feeding the first pretreated stream to a first centrifuge for centrifugal separation, producing a first liquid centrifuged stream, and a second liquid stream, and feeding the first liquid centrifuged stream to a second centrifuge producing a resultant centrifuged stream of recoverable oil and a water phase centrifuged stream which can be treated further or fed back to a source for re-use. The source may be a facility from the group including refineries, chemical plants, paper mill plants, and oil and gas processing facilities.

The invention relates to a method for preparing a length-diameter-ratio nano-silver wire by a pH-value regulation solvothermal method. The method comprises the following steps of: preparing the following ethylene glycol solution, namely an ethylene glycol solution A of silver nitrate or silver acetate, an ethylene glycol solution B of polyvinyl pyrrolidone (PVP), an ethylene glycol solution C of water-soluble chloride and concentrated acid D; mixing the components according to a certain amount and fully stirring to form a final mixed solution; moving the final mixed solution into a reaction kettle; placing in an oven for reaction for a certain time; taking the reaction kettle out and cooling to room temperature to obtain mother liquid of the nano-silver wire; adding alcohol into the mother liquid for diluting, and removing supernatant liquor to obtain a precipitate; and repeatedly performing centrifugal separation, and thus obtaining nano-silver wire dispersion liquid uniformly dispersed in the alcohol. The method is simple, high in efficiency and low in cost, and can prepare high-quality nano-silver wires within a wider range of reaction condition; and prepared products are high in length-diameter ratio, good in length uniformity and low in impurity content.

A dust collector cup working in the principle of fall centrifugal separation, consists of cup body (13), outlet (3) on the cup body (13), inlet (1) tangential to the circumferential wall of the cup body (13), and a separator settled in the cup body (13). The separator is composed of outlet tube (9), inlet (6) on the wall of the outlet tube (9), and the isolating shield (7) under the inlet (6) of the outlet tube (9), with the outlet tube (9) linked to the outlet (3) of the cup body (13). The fall between the horizontal positions of the lower end of inlet of the cup body (13) and the upper end of the inlet (6) of the outlet tube (9) is 0-140 mm.

A sewage treatment system is revealed. Water with contaminants is drawn from sources to the sewage treatment system for automatic and fast water purification. Thus clean drinking water is generated. The water with contaminants is sent to a treatment tank by a motor. Then non-toxic and odorless chemicals are sprayed in the treatment tank. By stirring and mixing of movable blades, the contaminants are coagulated and precipitated into a funnel under the treatment tank to be discharged. Next clean water in the treatment tank is sent to a centrifuge separator to be filtered and dehydrated by centrifugation. Water comes out from the centrifuge separator is drinking water. The sewage is converted into clean water. The system can provide clean safe drinking water to regions without water treatment plants.

A flexible metal support device for a rotatable centrifuge rotor (2) provided in a frame member (1) by a bearing member (4). The support device comprises a support element (7) provided between the bearing member (4) and the frame member (1), and arranged to absorb relative movements between the centrifuge rotor and the frame member. The support element (7) comprises an inner mounting portion, essentially immovable in relation to the bearing member (4), and an outer mounting portion, essentially immovable in relation to the frame member (1). Moreover, the support element (7) comprises three flexible connecting portions which each extends between the inner and outer mounting portions and is arranged to absorb radial and axial relative movements between the centrifuge rotor and the frame member. Furthermore, the inner portion, the connecting portions and the outer portion form an integrated unit manufactured in one piece of metal material.

A process for producing a purified product of green tea extract, which includes subjecting an aqueous solution of green tea extract to solid-liquid separation by filtration and / or centrifugal separation to obtain another aqueous solution of green tea extract, said another aqueous solution having a turbidity of from 0.2 to 2.0 as measured with a concentration of non-polymer catechins in it adjusted to 1 wt %, and then allowing the another aqueous solution of green tea extract to pass through a polymer membrane having a membrane pore size of from 0.05 to 0.8 μm such that the turbidity of the another aqueous solution of green tea extract is reduced to lower than 0.2 as measured with a concentration of non-polymer catechins in it adjusted to 1 wt %.

Bitumen extraction done using a process comprising: (a) preparing a bitumen froth comprising particulate mineral solids and hydrocarbons dispersed in aqueous lamella in the form of an emulsion; (b) adding a sufficient amount of a paraffinic solvent to the froth to induce inversion of the emulsion and precipitate asphaltenes from the resultant hydrocarbon phase; (c) mixing the froth and the solvent for a sufficient time to dissolve the solvent into the hydrocarbon phase to precipitate asphaltenes; and (d) subjecting the mixture to gravity or centrifugal separation for a sufficient period to separate substantially all of the water and solids and a substantial portion of the asphaltenes from the bitumen; wherein a separation enhancing additive is present in the process. The separation enhancing additive is a polymeric surfactant that has multiple lipophilic and hydrophilic moieties, which can effect easier handling of asphaltene sludges and less foaming during solvent recovery.

The invention discloses a wastewater evaporation concentration process and a wastewater evaporation concentration device system. The process comprises the following steps of: delivering softened wastewater to be treated to a mechanical vapor recompression (MVR) system to perform evaporation and concentration, compressing the generated secondary steam and then delivering the compressed steam to an evaporator to recycle, delivering the concentrate to a triple-effect mixed flow forced circulating evaporation crystallization system to perform evaporation and crystallization, performing solid-liquid centrifugal separation on the crystallized concentrate and crystal grains, returning the separated mother solution to a stock solution tank or continuously performing evaporation and crystallization, and reclaiming the separated crystal, wherein the secondary steam generated by evaporation and crystallization is recycled for the evaporation crystallization system. After the wastewater is evaporated and concentrated by adopting the process of mechanical vapor recompression circulating evaporation and triple-effect mixed flow forced circulating evaporation crystallization, the wastewater does not need to be discharged to the ground water area, and the wastewater is discharged in a form of steam or closed and embedded in a form of sludge or the like, so the purpose of zero discharge of the wastewater can be fulfilled; and the process system has high heat efficiency, low energy consumption, energy conservation, great reduction in running cost, low temperature difference, low corrosion, difficult scale formation and long equipment service life.

The invention provides a substrate with surface-enhanced Raman scattering activity and a preparation method thereof, and the method comprises the following steps: the glass base surface is subjected to hydroxylation and amination treatment; catalytic hydrolysis is carried out on ethyl orthosilicate under the alkali condition by taking alcohol as a solvent; Silica microspheres with even size and smooth surface are prepared by an oscillation method; silane coupling agent of which the tail end is provided with amino is assembled on the surface of the silica microspheres; silver sol obtained by reducing sodium borohydride to silver nitrate through oscillation is assembled on the surface of SiO2-NH2NPs, and is diffused in water again after centrifugal separation and washing by distillated water; self assembly is carried out on the silver sol after being placed in SiO2@Ag NPs dispersion for 6-12h; the SERS active substrate is obtained after taking out from water and drying. In the SERS active substrate of the invention, the active particles and the substrate are combined firmly, thus being applicable to detecting unimolecular Raman signals in aqueous solution; the substrate can be used for SERS detection repeatedly, thus improving repeated utilization ratio of the substrate.

The invention relates to a graphene-coated mesoporous metallic oxide, and a preparation method and use thereof. The preparation method for the graphene-coated mesoporous metallic oxide comprises the following steps of: 1) synthesizing mesoporous metallic oxides with different pore passage structures by taking mesoporous silicon dioxides with the different pore passage structures as templates; 2) preparing a graphene oxide by using an oxidation method; 3) absorbing mesoporous metallic oxide particles on the surface of the graphene oxide by using a heterocoagulation method; 4) reducing the graphene oxide into graphene by adding a reducing agent; and 5) performing centrifugal separation, washing and drying. The graphene-coated mesoporous metallic oxide provided by the invention has high electrochemical properties, and can be used as an electrode material of a lithium battery.