Thermal crosslinking of collagen immobilized on poly(acrylic acid) grafted poly(ethylene terephthalate) films

Graft polymerization of acrylic acid onto plasma‐treated poly(ethylene terephthalate) (PET) films was used to prepare surfaces suitable for collagen immobilization by dip‐coating. Such surfaces could be used as matrices for smooth muscle cell cultures in tissue engineering. Contact angle measurements showed that plasma‐treated and grafted PET films undergo considerable surface reorganization during storage under ambient conditions. However, after collagen immobilization the contact angle remained relatively stable. The amount of collagen initially attached to the film surface increased with increasing poly(acrylic acid) graft density, but subsequent washing in water led to significant collagen loss. This loss could nevertheless be substantially reduced by thermal crosslinking of the collagen in the range 110–130 °C. Atomic force microscopy (AFM) observations suggested that the washed crosslinked collagen has a very similar structure to that of the un‐crosslinked collagen. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1874–1880, 2002     

The removal of dichloromethane from atmospheric pressure air streams using plasma-assisted catalysis

Plasma-assisted catalysis was used for the destruction of 500 ppm of dichloromethane, CH₂Cl₂ (DCM), in gas streams of air using a non-thermal, atmospheric pressure plasma utilising a dielectric packed bed. The combination of plasma and catalyst gave improved destruction of DCM. Eight catalysts which including alumina, TiO₂ and various zeolites were investigated with the finding that alumina in a one-stage reactor configuration and TiO₂ and HZSM-5 in two-stage configurations gave the best DCM destructions. The sodium zeolites are capable of reducing by 50% the unwanted NO_x by-products, formed by plasma processing in air. The nature of the catalyst is important in terms of the destruction efficiency, end-product selectivity and NO_x reduction.     

Combination of non-thermal plasma and heterogeneous catalysis for oxidation of volatile organic compounds: Part 2. Ozone decomposition and deactivation of γ-Al2O3

The role of ozone was studied for two different configurations combining non-thermal plasma (NTP) and heterogeneous catalysis, namely the use of a gas phase plasma with subsequent exposure of the effluent to a catalyst in a packed-bed reactor (post-plasma treatment) and the placement of the catalyst directly in the discharge zone (in-plasma catalysis). Non-porous and porous alumina and silica were deployed as model catalysts. The oxidation of immobilised hydrocarbons, toluene as a volatile organic compound and CO as an inorganic pollutant were studied in both operational modes.

While conversion and selectivity of hydrocarbon oxidation in the case of catalytic post-plasma treatment can be fully explained by the catalytic decomposition of O₃ on γ-Al₂O₃, the conversion processes for in-plasma catalysis are more complex and significant oxidation was also measured for the other three materials (-Al₂O₃, quartz and silica gel). It became obvious that additional synergetic effects can be utilised in the case of in-plasma catalysis due to short-lived species formed in the NTP.

The capability of porous alumina for ozone decomposition was found to be correlated with its activity for oxidation of carbon-containing agents. It could be clearly shown that the reaction product CO₂ poisons the catalytic sites at the γ-Al₂O₃ surface. The catalytic activity for O₃ decomposition can be partially re-established by NTP treatment. However, for practical purposes the additional reaction pathways provided by in-plasma catalytic processes are essential for satisfactory conversion and selectivity.     

工业喷漆的环境污染研究

化工企业对环境的影响较大,其制造的化工产品严重威胁着人们的健康。近年来,随着化工企业的规模越来越大,其带来的环境污染问题也越来越严峻。就工业喷漆对环境污染的状况和治理措施进行了分析、探究。     

等离子喷涂羟基磷灰石涂层

羟基磷灰石由于具有优良的生物性能，被广泛应用于生物材料领域，而等离子喷涂制备羟基磷灰石涂层是应用最为广泛的制备方法之一。在综合国内外献的基础上，本从羟基磷灰石的本征性能、喷涂工艺的影响、结合强度和梯度涂层等方面进行综述。     

Graft polymerization of acrylic acid onto polyphenylene sulfide nonwoven initiated by low temperature plasma

Graft copolymerization of acrylic acid (AA) onto polyphenylene sulfide (PPS) nonwoven initiated by low temperature plasma was studied. The effects of various conditions on graft reaction and the grafting rate were investigated. SEM images showed that PPS nonwoven was grafted, and the graft copolymerization only occurred on the surface of PPS. It may be due to the chain transference going with the graft copolymerization. It was found that with the increasing of plasma power, treatment time, space between electrodes, monomer concentration, and temperature of graft polymerization, the grafting rate increased at first, went to the top, and then decreased. The PPS nonwoven surface graft reaction could be optimized by the following processing conditions: 120 s of plasma treatment time, 50 W of plasma power, 1.5 cm of space between electrodes, 30% (w/w) of monomer concentration, and 50°C of temperature of graft polymerization. Measurement of XPS showed that the peak of C1s of graft polyacrylic acid was existed, and the peak area increased with the increase of the grafting rate. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5884–5889, 2006     

Granulation of a hardmetal powder for spark plasma sintering

A fluidized bed granulation method, pressure swing granulation (PSG), was applied to granulation of a hardmetal powder without pressing lubricants for making the upstream process of spark plasma sintering (SPS) more efficient.

The properties of the granules were examined and compared with those of spray dried granules and extruded ones under the present system using a sieve.

Spherical granules between 0.15 and 0.84 mm in diameter difficult to obtain by the spray drying were obtained with high yield. The flowability of the granules was far better than that of spray dried granules and similar to that of extruded ones. Iron contamination and oxidization during pressure swing granulation were tolerable to the real production.     

超滤膜等离子体改性分离大豆蛋白的研究

分别用氧气和氩气等离子体对醋酸纤维素超滤膜进行表面改性,用大豆分离蛋白溶液进行超滤实验,结果表明等离子体处理后膜的接触角变小,亲水性能大大增强,超滤过程可以在保持截留率不变的情况下使膜的透水率增大2～3倍,同时膜的抗污染性能增强。研究发现在相同的等离子体反应条件下,氩气的处理效果优于氧气。     

Measurement of zeolite,silicate, and phosphate in laundry detergent products by inductively coupled plasma atomic emission spectrometry

This paper reports the development of a method for simultaneously measuring zeolite, silicate, and phosphate in laundry detergent products by inductively coupled plasma atomic emission spectrometry. A sample is decomposed under alkaline oxidative conditions to decompose zeolite, silicate, phosphate, and organic substances. Then hydrochloric acid is added to the decomposed solution to dissolve aluminum hydroxide precipitate before analysis. This sample preparation procedure was investigated by using a total organic carbon analyzer and was confirmed to be applicable to simultaneous measurements of zeolite, silicate, and phosphate. Relative standard deviation for the analysis is less than 2.1%, recovery is more than 99.0%, and the calibration curve gives a correlation coefficient ofR=1.000. The detection limit of this method for aluminum and silicon is 0.1%, and for phosphorus, 0.2% by weight in the product. This method is applicable to various laundry detergent products that contain zeolite, silicate, or phosphate and is five times faster than the three wet chemical methods.     

Multi：DTN中一种自适应的消息转发算法

为了充分利用DTN中各节点资源,减少Epidemic Routing、spray and wait中不区分各节点资源不同,提出了一个基于节点密度、节点运动速度、生存期、节点缓存大小诸多因素,来进行消息转发的算法multi。通过仿真实验表明,multi算法较Epidemic Routing、spray and wait算法在消息成功传输率、平均延迟、网络开销、消息在缓存中滞留的时间上都有明显改善。