经用

Nurse 2.1 nurse commonly it is 10min of ～ of 5min of patient bubble foot with Wen Shui every night, use bibulous towel gentleness and wipe thoroughly, besmear equably with vegetable oil next at the patient double sufficient, massage gently absorb adequately what make, in order to achieve bit of skin softness, cleared scale, avoid weather-shack end. Clip fingernail shoulds not be too short, lest injure armour channel afterwards to send infection, do not stick adhesive plaster of cutaneous having damage, notice sufficient ministry heat preservation, footgear is appropriate, do not pass too small, excellent, close.

足背动脉搏动减弱7例，消失3例，缺血性溃疡4例，四周神经病变2例，表现为深浅感觉减退，经综合治疗20d～40d后治愈8例，好转4例。2护理2.1一般护理每晚用温水为患者泡脚5min～10min，用吸水毛巾轻柔而彻底擦干，然后用植物油均匀涂于患者双足，并轻轻按摩使之充分吸收，以达到皮肤柔软、清除鳞屑、防止干裂的目的。

This article uses the microwave oven separately to use 700W,336W processing for 3min on pretreatment of three vegetables(celery,greengrocery and green soy bean),andusing the ultrasonic wave extraction process and 70％methyl alcohol to withdraw,then Uses the spectrophotometer method to determine and compare total flavonoid content of the three vegetables in which two samplewere processed by microwave,and the other was fresh.

本文利用微波炉对新鲜的三种常食蔬菜进行处理，分别用700W，336W处理3分钟，采用超声波提取法用70％的甲醇进行提取，然后用分光光度法对三种蔬菜未经微波处理的新鲜样品和经两种微波处理的样品进行总黄酮含量的测定和比较。

In the spiral pipe heat exchanger exports terminal, the ammonia steam temperature has been heated up 85 ℃--95 ℃, by now, the ammonia steam had the 45kg-55kg/cm2 ammonia steam pressure, sent in the ammonia steam turbine through the constant temperature pipeline, impelled ammonia steam turbine revolving, led the generator electricity generation;After the ammonia steam makes the merit release energy, the temperature drop, the returns ammonia storage tank, passes through again adjusts the press pump to press into the spiral pipe-type heat exchangers to carry on the next circulation;Including the ammonia steam turbine entire ammonia steam road is becomes the independent closed cycle system, is isolates completely with the outside air;The ammonia steam only plays the carryhome and the shift energy role, in the electricity generation process does not consume the actuating medium, the stored energy carrier water also is only gets up the carryhome and the shift energy function,The waterway also is from becomes the independent closed cycle system, in the electricity generation process also the needless water consumption, through the actuating medium ammonia steam and the stored energy carrier water unceasing shuttle service, transforms through the heat interchanger the solar energy as the actuating medium ammonia steam heat energy and the kinetic energy,With the aid of the ammonia steam turbine heat - machine transformation function and the generator machine - electricity transformation function, has realized the solar energy hot - electricity entire conversion process, transforms continuously the solar energy into the electrical energy, power supply for foreign;The low temperature generating system must solve three big technical keys:One, the anticorrosion (has actuating medium has strong corrosiveness), two is Explosion-proof (Some actuating medium Can have the detonation with the air mix when divulging, controls warm malfunction, elevates temperature suddenly also can have detonation), three is guards against the revolution axis divulging

以太阳能低温发电系统为例，低温发电方法是这样进行的：以水作为储能载体的太阳能采集器将太阳能采集起来，将水温提升至85℃--98℃；用氨作为工作介质储于氨储罐及氨汽路中；采用螺旋管型热交换器；用调压泵将氨储罐中的氨汽压入螺旋管型热交换器的螺旋管内，用调压泵将携带太阳能的85℃--98℃的储能载体热水压入螺旋管型热交换器的螺旋管外壁空间进行循环式热交换，在热交换器的螺旋管出口端，氨汽温度已被加热到85℃--95℃，这时，氨汽具有45kg—55kg/cm2的氨汽压力，通过恒温管道送入氨汽轮机，推动氨汽轮机旋转，带动发电机发电；氨汽作功释放能量后，温度下降，返回氨储罐，再经调压泵压入螺旋管型热交换器进行下一次循环；包括氨汽轮机在内的整个氨汽汽路是自成独立的封闭循环系统，与外界空气是完全隔绝的；氨汽只起携带和转移能量的作用，发电过程中并不消耗工作介质，储能载体水也是只起携带和转移能量的作用，水路也是自成独立的封闭循环系统，发电过程中也不消耗水，通过工作介质氨汽和储能载体水的不断循环运行，通过热交换器将太阳能转化为工作介质氨汽的热能和动能，借助氨汽轮机的热—机转化功能和发电机的机—电转化功能，实现了太阳能的整个热—电转化过程，将太阳能源源不断地转变为电能，对外供电；低温发电系统要解决的三大技术关键：一是防腐（有的工作介质具有较强的腐蚀性）、二是防爆（有的介质泄漏与空气混合会产生爆炸，控温失灵，急剧升温也会产生爆炸）、三是防轴漏（汽轮机是动态旋转体，必须解决工作介质的防轴漏问题）。

Audio and video steams accord with MPEG-2 standard can form PES after packeted, and then PES steam can form tranport stream after multiplexer. The transmitter conduct a number of transport stream multiplexing ,then send out the signal via satellite,cable or terrestrial transmitting station.The end user receiver picks up the DTV signal,demultiplexes it and finally the MPEG-2 decoder presents the decoded audio and video stream to the user.

按MPEG-2标准编码后的音频视频流经打包之后形成打包基本流，PES经过复用之后形成传输流，发射端进行多个传输流复用，最后通过卫星、有线电视及开路电视等不同媒介传输方式进行传输；接收端经信号接收，解复用，解码后显示给用户原先的音、视频节目。

Methods Quality control sera with low, medium and high determined values were prepared and tested with a set of SCAg reagents for 20 batches and times.

制备质量控制低、中、高3种定值血清，用SCAg试剂经20批次测定绘制质控图，按WHO评价标准判断可信度；用批量QC血清插入血吸虫病现场与普查的样本中用SCAg试剂检测，在流行区实验室间进行单盲测试；对不同感染程度的血吸虫病流行区及非流行区采集的未知样本的EQA批量检测；用急性感染血清观察SCAg试剂检测的Hook效应。

The disinfection of the hand, can wash his hands via water of commonly used flow, soap, in anteprandial, hind, after the contact pollutes article, had better use contain 250 - disinfectant of 1000mg ∕ L1210 or 250-1000mg ∕ L are effective disinfectant of carry out hand disinfects iodic iodic bend over or the town that use classics sanction.

手的消毒，可经常用流动水、肥皂洗手，在饭前、便后、接触污染物品后最好用含250－1000mg∕l1210消毒剂或250-1000mg∕l有效碘的碘伏或用经批准的市售手消毒剂消毒。

Pneumophila serogroup 5 antibody to develop two immuo-colloidal gold tests respectively. Main works listed below as:1、Preparation and identification of polysaccharide antigen of L. pneumophila Bacteria of LP1 ~ 7,9 and 10 were cultured on yeast agar buffer activated carbon for three to five days at 37℃, 5%CO2. Protein-free polysaccharide antigens were obtained after harvest in cells, extraction, deproteinization, dialysis and other steps. Their immunogenicities were verified by ultraviolet spectrophotometer full-wavelength scanning and Western blotting.2、Preparation and identification of rabbit anti-LP1 antibodies and rabbit anti-LP5 antibody Rabbit anti-LP1 and anti-LP5 antibodies were purified after rabbits were immuned with antigens isolated as described above. The purities of both antibodies were above 80% and the titer of blood serum 1:32 tested by double antibody sandwich assay.3、Development of colloidal gold immunochromatographic assay kit The size of colloidal gold particles in the kit was 25nm. The optimal concentrations for antibodies were 30μg/ml and the sensitized concentrations of NC membrane were 5 mg/ml.

主要研究工作从以下几个方面进行：1、LP1~7、9和10型多糖抗原的制备与鉴定将LP1~7、9和10型菌株分别接种在缓冲活性炭酵母琼脂培养基上，37℃、5%CO2的条件下培养，3~5天后洗下菌苔，经抽提、除蛋白、透析等步骤后得到基本无蛋白的LP多糖抗原，经紫外分光光度仪全波长扫描及Western blotting验证其抗原良好。2、兔抗LP1抗体和兔抗LP5抗体的制备与鉴定分别用LP1、LP5型多糖抗原免疫家兔，采用琼脂糖双向扩散试验检测，两种抗体血清效价均为1：32；饱和硫酸铵法提取抗体，SDS-PAGE检定其抗体纯度均达到80%以上。3、胶体金免疫层析检测试剂的初步研制采用柠檬酸三钠还原法制备约25nm大小的胶体金颗粒；分别制备兔抗LP1抗体、兔抗LP5抗体的金标探针，两种抗体的最适标记量均为30μg/ml；选择适当孔径的微孔滤膜为载体包被两种抗体，NC膜包被浓度均为5mg/ml。

Production of epsilon-glycolylnium is carried out by Beckman rearrangement reacting for cyclohexanone-oxime under the existence of solvent to obtain epsilon-glycolylnium contained mixture, crystalline separating for the mixture to obtain crude epsilon-glycolylnium crystal, dissolving by arene, extracting by water, adsorbing by resin hydrogenation catalyzing to obtain the final product. The value of potassium permanganate is less than 5, extinction value is less 0.05, volatile alkali is less than 0.5meq/kg and alkalinity is less than 0.05meq/kg.

本发明涉及一种ε―己内酰胺制备方法，其特征为：在溶剂存在下，环己酮肟经贝克曼重排反应，得到含有ε―己内酰胺的混合物，该混合物结晶分离后，得到粗ε―己内酰胺晶体用芳烃溶解，然后用水萃取，再经树脂吸附、催化加氢后，得到99.995％以上的高纯度的ε―己内酰胺，其质量指标为高锰酸钾值小于5，消光值小于0.05，挥发性碱小于0.5meq/kg，碱度小于0.05meq/kg。

When the pulverized material has been properly sized, mixed with the additive in the amount determined by testing, laid and compacted to the required density, surfaced with a chip seal coat, thin hot mix overlay or other light surfacing, a long lasting, low cost pavement can be constructed with a minimum of new material.

只有当被压碎的材料已制成合适的大小，混合了经测试确定的适量添加剂，铺设并压紧至要求的密度，再用一层碎片封闭层、热混薄覆盖层或其它轻质的材料铺平表面，经时效处理后，方可达到以用量最少的新材料构筑出低成本路面的目标。

The apxⅢA gene of Actinobacillus pleuropneumonie was amplified by PCR. The amplified DNA fragment 3 466bp was cloned into pMD18-T. After R.E. analysis and sequencing, the apxⅢA gene in pMD18-T was ligated into pBluescripⅡSK, the recombinant expression plasmid pET-28b/apxⅢA was constructed and analysed with R.E., the protein of apxⅢA gene expressed in E.coli BL21 was detected by Western blotting.

因胸膜肺炎放线杆菌的致病性主要是由毒素决定的，故参照猪胸膜肺炎放线杆血清2型菌株的序列(GenBankL1 2 1 4 5)设计了一对特异性引物，用PCR的方法扩增apxⅢA基因并得到了长 3 466bp的片段，然后将其克隆到pMD 1 8T中，经酶切鉴定和序列分析表明克隆是成功的；再将apxⅢA插入到原核表达载体pET 2 8b后，转化BL2 1 (DE3)，在IPTG诱导下获得高效表达，经Westernblotting检测证实表达产物有活性。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。