Preparation technology of ultra-fine powders of Auricularia auricular

Conventional mechanical method and mechanical method combined with vacuum freeze-drying technology were used to make the ultra-fine powders of edible fungus (Auricularia auricular). The content of basic nutrients, amino acid, micro structure and their properties of raw edible fungus and the edible fungus powders obtained with the two methods were analyzed and compared. The granularity size and micro-structure of the pulverized samples were analyzed by SEM and TEM technology. The average granularity size of the edible fungus powder obtained with mechanical method was 1–5 μm, while that obtained with mechanical method combined with vacuum freeze-drying process was 0.5–1 μm. The ultra-fine powders of edible fungus obtained with the two methods had better water recovery capability and quality, and their preserving time was longer than that of raw edible fungus. All the properties of the ultra-fine powders of edible fungus obtained with the vacuum freeze-drying technology were evidently superior to that of the conventional mechanical method. Keywords Auricularia auricula - Edible fungus - Ultra-fine powders - Vacuum freeze-drying CLC number TS205 Document code B Biography: YANG Chun-yu (1975), female, Ph. D. in Engineering Technology Center of Forestry and Wood Workine, Machinery, Northeast Forestry University, Harbin 150040, P. R. China.Responsible editor: Zhu Hong

Optimal Conditions for Preparing Ultra-Fine CeO_2 Powders in A Submerged Circulative Impinging Stream Reactor

Cerium carbonate powders were produced in a submerged circulation impinging stream reactor （SCISR） from Ce（NO3）3· 6H2O. NH4HCO3 was used as a precipitant in the reaction. Cerium carbonate powders were roasted to produce ultra-fine cerium dioxide （CeO2） powders. The optimal conditions of such production process were obtained by orthogonal and one-factor experiments. The results showed that ultra-fine and narrowly distributed cerium carbonate powders were produced under the optimal flowing conditions. The concentrations of Ce（NO3）3 and NH4HCO3 solutions were 02,5 and 0.3 mol · L^-1, respectively. The concentration of PEG4000 added in these two solutions was 4 g · L^-1. The stirring ratio, reaction temperature, feeding time, solution pH, reaction time and digestion time were 900 r · min^- 1,80 ℃, 20 min, 5 - 6, 5 min and 1 h, respectively. The final product, CeO2 powders, was obtained by roasting the produced cerium carbonate in air for 3 h at 500 ℃. The finally produced CeO2 powders were torispherical particles with a narrow size distribution of 0.8 -2.5 μm. The crystal structure of CeO2 powders belonged to cubic crystal system and its space point 5 group was OH^5-FM3M. Under optimal conditions, powders produced by SCISR were finer and more narrowly distributed than that by Stirred Tank Reactor （STR）.

DYNAMIC RHEOLOGICAL BEHAVIOR OF POLYPROPYLENE FILLED WITH ULTRA-FINE POWDERED RUBBER PARTICLES

Dynamic rheological characteristics of polypropylene (PP) filled with ultra-fine full-vulcanized powdered rubber (UFPR) composed of styrene-butadiene copolymer were studied through dynamic rheological measurements on an Advanced Rheometric Expansion System (ARES). A specific viscoelastic phenomenon, i.e. 'the second plateau', appeared at low frequencies, and exhibits a certain dependence on the amount of rubber particles and the dispersion state in the matrix. This phenomenon is attributed to the formation of aggregation structure of rubber particles. The analyses of Cole-Cole diagrams of the dynamic viscoelastic functions suggest that the heterogeneity of the composites is enhanced on increasing both particle content and temperature.

An improved sodium silicate binder modified by ultra-fine powder materials

This paper presents a new method of modifying sodium silicate binder with ultra-fine powders. The sodium silicate binder modified by ultra-fine powder A and the organic B can reduce the addition amount of the binder. The results indicate that the 24 h strength has increased by 39.9% at room temperature and the residual strength has decreased by 30.7% at 800℃, compared to the conventional sodium silicate. An available material to improve the moisture resistance was also found by adding about 2% more inorganic C, and it can increase the moist strength by 20%. In the end, the microanalyses are given to explain the modifying machanism, i. e., the ultra-fine powder A can refine the sodium silicate binder to avoid holes in the binder bond, which can increase the 24 h strength at room temperture, and can lead to more cracks in the bond after the molding sand is heated to 800℃. This is because of the stress caused by the new eutectic complex of modified sodium silicate binder.

Hydrogen Reduction:A Novel Method of Synthesizing Ultra-fine Chromic Oxide Powder

The ultra-fine chromic oxide powder was prepared by a novel gas-solid reduction reaction.Na2CrO4 was firstly reduced with hydrogen at 400-600 ℃.The obtained reduction products,mainly the mixture of NaCrO2 and sodium hydroxide（NaOH）,were converted into chromic oxide through hydrolysis followed by calcination.The obtained chromic oxide product was characterized by powder X-ray diffraction（XRD） and SEM.The results show that the hydrolysis process of sodium chromite is the key step and lower reduction temperature helps intensify the hydrolysis process.

Strengthening of HT250 by modified ultra-fine ceramic powders

In this study, three kinds of modified ultra-fine ceramic powders marked A, B and C, which were prepared by each of three different modifiers mixing with a commercial SiC, were added to HT250 cast iron, respectively, and the effects of the modified ultra-fine ceramic powders on microstructure, mechanical properties and wear resistance were studied. Metallographic examination, tensile test, scanning electron microscopy, and three-dimensional surface topography were applied to analyze and compare the samples containing modified powder with the original samples. The results showed that the most obvious modification effect among the powders was seen in the sample containing powder A, with the graphite and eutectic cells being refined, the tensile strength being increased by 36.9%, and the wear resistance being improved by 45.5% and 47.2% under loads of 150 N and 300 N, respectively. The improvements of mechanical properties and wear resistance in the HT250 cast iron with the modified ultra-fine ceramic powders were attributed to the synergistic effect of the grain refinement with the powder acting as a hard particle phase and the lubrication by the graphite.

Preparation of Ultra-fine Salbutamol Sulfate Particles by Reactive Precipitation and Characterization of Dry Powder Inhalant

The preparation of ultra-fine particles of salbutamol sulphate （SS） was accomplished with a reactive precipitation pathway, in which salbutamol and sulphuric acid were Used as reactants with the solvents of ethanol.The effects of sulphuric acid concentration, reaction temperature, stirring rate, and reaction time onthesize of the particle were investigated. A binary mixture composed of lactose and SS was prepared to evaluate SS. The results showed that ultra-fine SS particles with controlled diameters ranging between 3 μm and 0.8 μm and with a narrow distribution could be achieved. The morphology consisting of clubbed particles wassuccess.fully obtained. The purity of the particles reached above 98% with-UV detection. The dose- of dry powder inhalation was obtained by blending the particles with recrystallized lactose, which acted as a carrier. The deposition quantity of the drug in breathing tract was estimated using a twin imPinger apparatus. Compared with the Shapuer powder （purchased in the market）, the results showed that SS_particles had more quantifies.subsided in simulative lung.. _

Preparation of Well Dispersed and Ultra-Fine Ce(Zr)O_2 Mixed Oxide by Mechanochemical Processing

Ultra-fine CeO_2-ZrO_2 mixed oxide was successfully synthesized by wet-solid phase mechanochemical processing, Ce_2(CO_3)_3·8H_2O, ZrOCl_2·xH_2O and ammonia were used as reactants. It is found that the crystalline Ce_2(CO_3)_3·8H_2O and ZrOCl_2·xH_2O are changed to amorphous cerium and zirconium hydroxide precursor after milling with ammonia, and Ce_(0.15)Zr_(0.85)O_2 mixed oxide with pure tetragonal phase structure and medium particle size(D_(50))less than 1μm is formed by calcining precursor over 673 K. The XRD patterns indicate that the crystal unite size increases with rising calcining temperature due to crystal growth. However, the particle size and BET surface area of the Ce(Zr)O_2 mixed oxide decreases with rising calcining temperature, which may be attributed to the contract of particles and the vanish of holes inside grains.

ELECTRORHEOLOGICAL PROPERTIES OF TALC POWDER/SILICONE OIL SUSPENSIONS UNDER DC FIELDS

In this study, the electrorheological （ER） behavior of suspensions prepared from d50 = 2.4 lam talc powder, dispersed in insulating silicone oil （SO） medium was investigated. Sedimentation stabilities of suspensions （c = 5 wt%） prepared using these talc powder powders were determined to be 78 days. The ER activity of all the suspensions was observed to increase with increasing electric field strength, concentration and decreasing shear rate. The shear stress of talc powder suspensions increased linearly with increasing concentrations of the particles and with the applied electric field strength. Electric field viscosity of all the suspensions decreased sharply with increasing shear rate and showed a typical shear thinning non-Newtonian visco-elastic behavior. Effects of frequency on the ER activity of talc powder/SO system were also investigated.

Preparation of Ultra-nano Talcum in Sand Mill and Its Application in the Polypropylene

The grinding of ultra-fine talcum powder and its application in a polypropylene （PP） matrix were investigated. Ultra-fine talcum powder was prepared by adjusting the grinding parameters of the physical milling process. The talcum powder exhibited polymodal distribution. The layered morphology of talcum particles in a horizontal sand mill was rarely damaged or destroyed. PP-talcum nanocomposites were prepared by melt blending using a twin-screw extruder. Nano talcum can be seen as a single particle, although it is not very apparent. The bending strength of talcum-filled PP was gradually increased by approximately 28%. The impact strength linearly decreased as the filler weight ratio increased. The overall maximum improvement in mechanical properties was recorded when the filler ratios increased from 15 wt% to 20 wt%.

Synthesis and Characterization of Nano-sized Boron Powder Prepared by Plasma Torch

Hydrogen thermal plasma jet was employed to prepare nano-sized boron powder with hydrogen reduction of BCI3. The maximum yield of nano-sized boron powders was about 50% with the operational conditions of H2/BCl3 of 4.5：1, total feed of 4.9 m3/h, and plasma power of 25 kW. The samples were analyzed by X-ray diffraction （XRD）, field emission scanning electron microscopy （FE-SEM）, and inductively coupled plasma - mass spectrometry （ICP-MS）, inductively coupled plasma - atomic emission spectrometry （ICP-AES）, inductive combustion infrared absorption （ICIA） and infrared thermal conductivity of oxygen and nitrogen analyzer （ITCA）. The results show that the boron powders have different crystal structures with higher dispersion and purity. The average diameter is about 50 nm, and the purity is 90.29% or so. This new technology can use simple process to produce high quality boron powders, and is feasible for industrial production.

Preparation of Reactive Powder Concrete Using Fly Ash and Steel Slag Powder

To decrease the cement and SF content of RPC by using ultra-fine fly ash （UFFA） and steel slag powder （SS）, the effect of these mineral admixtures on compressive strength of RPC were investigated. The experimental results indicate that the utilization of UFFA and SS in RPC is feasible and has prominent mechanical performance. The microstructure analysis （SEM and TG-DTG-DSC） demonstrated that the excellent mechanical properties of RPC containing SS and UFFA were mainly attributed to the sequential hydration filling effect of the compound system.

Preparation of Ultrafine Tungsten Powder by Sol-Gel Method

Sol-gel method was employed for the preparation of nanoscale tungsten powder. The effects of different preparation conditions on particle size were discussed and the optimum preparation condition was found. The products were characterized by X-ray diffraction, scan electron microscopy and so on. The results show that the intermediate is monoclinic WO3, its particle shape is approximately spherical, and the particle size distribution is narrow. The average particle size is about 60 nm. After deoxidization, WO3 turns into cubic tungsten powder with small particle size （average particle size about 120 nm） and narrow size distribution.

Crystal Structure of Ba_xSr_1-xTiO₃Fine Powder

Various compositions of the system BaxSr1-xTiO3 (BST) have been elaborated both as fine powders and ceramic monoliths, using the co-precipitation route within a warmed supersaturated solution of oxalic acid. The appropriate stoichiometry was determined from the mixtures of precisely titrated aqueous solutions of cations chlorides (SrCl2, BaCl2, and TiCl4). The reason of this process was to apply low sintering temperature in production of BST samples with ultra-fine powders. These powders primarily calcined at (850°C) for (5 hr) were used to elaborate ceramics after pellets sintering at (1200°C) during (8 hrs). Indeed, XRD patterns were confirmed that the samples are a pure phase and a perovskite cubic structural type at (x = 0, 0.5, 0.6). Whereas, (x = 0.7, 0.8, 0.9, 1) showed a tetragonal phase. There is agreement between the FTIR and XRD analysis, by the relation of the wave vector (K) and lattice constant. It was deduced a stimulated relation between (x) and (K). The results of TEM, they were clear that the lowest particle sizes investigated of BST powders nearly (36 - 50 nm).

添加复合稀释剂的低爆速乳化炸药的制备及性能

以玻璃微球和滑石粉共同作为稀释剂制备一种低爆速乳化炸药。观察不同质量分数的玻璃微球和滑石粉对乳化炸药形貌的影响,并对乳化炸药的爆速、猛度、空中爆炸冲击波压力及储存稳定性进行测试。实验结果表明,随着滑石粉质量分数的增加,乳化炸药的形貌由乳胶状逐渐向颗粒状转化,爆速呈线性下降,对玻璃微球质量分数为5%、10%、15%的乳化炸药,测得最低爆速分别为3440、2740、2188 m/s。而随着滑石粉质量分数的增加,猛度、空中爆炸冲击波峰值超压均呈非线性下降,当滑石粉控制在一定量时,冲击波正压作用时间变化不大,乳化炸药储存稳定性较好。这种低爆速乳化炸药成本低廉、爆轰性能可调、储存稳定性好,具有较好的实用性。

微波消解-火焰原子吸收光谱法间接测定小麦粉中的滑石粉

建立微波消解-火焰原子吸收光谱法测定小麦粉中滑石粉含量的方法。通过对消解系统酸用量和释放剂氯化锶加入量的优化,最终确定选用硝酸-氢氟酸体积比5∶1作为消解用酸,以每100 mL试样溶液中加入2.0 mL 15 g/L氯化锶溶液来达到消除干扰的目的,经过方法学验证,结果表明:在0.2~1.0 mg/L范围内线性良好,相关系数r为0.999354;在加入镁元素的含量分别为1153.8、2884.6、7692.3μg/g时,平均回收率分别为101.0%、102.0%和102.3%,方法的相对标准偏差为0.44%,检出限为0.0040 g/kg,定量限为0.0134 g/kg,实际样品测定结果满意。

Preparation and properties of Nd:YAG ultra-fine powders

Ultra-fine Nd：YAG powders with different doping concentrations were synthesized by sol-gel combustion method. The pure Nd：YAG could be prepared at the low temperature of 900℃. Ethanol could improve the dispersity of powders, and the average size of the ultra-fine powders was around 250 nm. The reflection spectrum showed that there were several apparent characteristic absorption peaks and the intensity of these peaks enhanced with the increasing concentration of Nd^3＋. The luminescence spectrum, which was excited by 808 nm wavelength, exhibited several obvious emission bands in the range of 900-1150 nm. The emission intensity of Nd：YAG powders increased until the Nd content was above 3 mol.% due to the fluorescent quenching effect.

滑石粉微波消解方法的比较研究

涉及滑石粉的质量分析需要将其由固态转化为易于分析的溶液状态,这个过程通常需要进行消解,微波消解是较常被选用的消解方法。现有报道的微波消解滑石粉的方法有多种,但它们的消解效果不尽相同。通过采用微波消解法,以医药用滑石粉为研究对象,将几种采用不同消解试剂和步骤的消解方法进行比较,对比其消解效果的差异。结果表明:硝酸无法消解滑石粉;氢氟酸消解液体系能够消解滑石粉,但是消解能力有限;氢氟酸消解体系辅以饱和硼酸溶液进行二次消解,能够消解更多的滑石粉。氟硼酸-硝酸-过氧化氢的消解体系有着很强的消解滑石粉的能力,且该体系试剂在常温下不腐蚀玻璃,后续检测无需赶酸。

新兰伯恩磨耗参数与胶料磨耗状态关系的研究

研究新兰伯恩磨耗设备试验参数(载荷、试样速度、滑移率和滑石粉落粉速度)与胶料磨耗状态的关系,通过观察胶料表面磨纹在不同磨耗参数下的情况,分析橡胶的磨耗机理。结果表明:载荷与磨耗速度具有较高的正相关性;试样速度与单位时间磨耗速度具有较高的相关性,但与单位距离磨耗速度基本无相关性;滑移率与磨耗速度的相关性较高,随着滑移率的增大,样品表面的磨纹愈发清晰,磨屑聚集情况逐渐加重;落粉速度与磨耗速度的关系相对复杂,当落粉速度小于0.3 cm^(3)·min^(-1)时,两者的相关性较低;当落粉速度为0.3~0.6 cm^(3)·min^(-1)时,磨耗速度随着落粉速度的增大而增大,此时可观察到样品表面磨屑的生长过程;当落粉速度大于0.6 cm^(3)·min^(-1)时,磨耗速度随着落粉速度的增大而迅速减小。

A new method of preparing NdB_(6)ultra-fine powders

Combustion synthesis method was used to prepare NdB_(6)ultra-fine powders with B_(2)O_(3),Nd_(2)O_(3)and Mg powders as the raw materials.The basic thermody-namic data of NdB_(6) were estimated.The standard forma-tion heat of NdB_(6) is-357.48 kJ·mol^(-1).The values of the heat capacity and the standard entropy are 96.87 and 86.60 J·K^(-1)·mol^(-1),respectively.The adiabatic tempera-ture of the reaction is 2726 K,which is higher than the thermodynamic criterion of 1800 K.This indicates that the combustion synthesis reaction of the B_(2)O_(3)-Nd_(2)O_(3)-Mg system could spontaneously take place by itself to generate NdB_(6).The NdB_(6) powders were characterized by X-ray diffractometer(XRD),scanning electron microscopy(SEM)and differential scanning calorimetry-thermo-gravimetry(DSC-TG).The results indicate that the com-bustion products consist of NdB_(6),MgO,and a few Mg_(3)B_(2)O_(6)and Nd_(2)B_(2)O_(6).The leached products consist of single NdB_(6) phase,and its purity is 98.6 wt%.When the sample preparation pressure is 20 MPa,the average parti-cle size of NdB_(6) powders is less than 500 nm.The antioxidant ability of NdB_(6) is very strong,which is oxi-dized step by step.The apparent activation energies of the oxidation reactions are 986.14 and 313.83 kJ·mol^(-1),respectively.In addition,the reaction orders are 4.10 and 3.75,respectively.