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101.
[目的]基于理论推导建立凸齿镇压器作业过程中的运动学和动力学模型。[方法]根据运动学中刚体做平面运动的瞬心定理和牵连运动为平动时质点的加速度合成定理,建立凸齿镇压器在不同工作阶段的运动参数模型;根据动力学中的动量定理、动能定理和冲量定理,建立凸齿镇压器工作状态中所需牵引力、凸齿与地面作用瞬间产生的冲击力和冲击能的参数模型。[结果]凸齿镇压器作业过程中所需的牵引力随着凸齿镇压器的自身质量和滚动阻力系数的增加而增大,而凸齿镇压器转动惯量的增加会降低凸齿镇压器所需牵引力;冲击过程中,凸齿镇压器的牵引速度越大、质量和转动惯量越大、冲击时间越短,则冲击力越大;凸齿镇压器冲击土壤时的冲击能随着凸齿的转动惯量、质量和质心竖直向下移动距离的提高而增加,而随土壤的弹性系数与土壤的塑性变形量的增加而减小。[结论]建立了凸齿镇压器在不同工作状态下运动学及动力学模型,分析并揭示了凸齿镇压器结构参数与运动参数间的相互联系,探索了凸齿镇压器冲击土壤的特征规律,为设计和优化其结构参数和运动参数提供了理论依据。 相似文献
102.
Three of the most commonly used veterinary antibiotics—enrofloxacin (ENR), sulfamethoxazole (SMX), and oxytetracycline (OTC)—were chosen as representative antibiotics for UV/H2O2 treatments. The objective was to determine the optimization of UV/H2O2 to remove antibiotics from aquaculture discharge water using response surface methodology. The degradation of the antibiotics was investigated under varying UV/H2O2 conditions in environments with different levels of pH, water matrices, humic acid, and constituent ions. The degradation results demonstrated that increasing the H2O2 dosage facilitated ENR degradation at a neutral pH while facilitating degradation of SMX and OTC at a slightly acidic pH. The optimum removal conditions for ENR, which was used in all influential effect experiments and the contact tank experiments, was obtained at 10 mM H2O2, a pretreated COD of 87.51 mg L−1, and an initial pH of 6.15. Among the tested anions, only the presence of Cl- showed slight positive effects on ENR degradation, due to the generation of secondary active radicals. During the reaction, the hydroxyl radical (OH) was present at a higher pH while singlet oxygen (1O2) was slightly present at a lower pH. The experimental results from H2O2 sequential addition indicated that freshly added H2O2 could quench the recently generated OH and therefore a high H2O2 concentration with frequent adding was not necessary. Our contact system reduced the ENR concentration in both the effluent reservoir and in the UV irradiation zone. The overall results supported the use of the UV/H2O2 system to treat remnant antibiotics in the discharge water. 相似文献
103.
《Communications in Soil Science and Plant Analysis》2012,43(2):220-230
Different relationships between soil-test methods results have been reported in several agricultural regions. Differences in the same soil-test procedure (e.g., soil/solution ratio) exist between soil-testing laboratories from different agricultural regions. Our objectives were to (1) determine the effect of soil/solution ratio on the amount of phosphorus removed by Bray 1 and Mehlich 3 methods, (2) compare the amounts of phosphorus removed by Bray 1 and Mehlich 3 in Mollisols from the Pampean region, and (3) determine whether soil/solution ratio affects the relationship between Bray 1 and Mehlich 3. Soil phosphorus availability was determined with two extractants (Bray 1 and Mehlich 3), using two soil/solution ratios (1:10 and 1:8, wt/v) in 72 soils (noncalcareous, loess-derived Molisolls) from the Pampean region. The amount of phosphorus removed was 20–24% greater when using 1:10 than 1:8 (wt/v) soil/solution ratio. This effect was significantly greater in Bray 1 than in Mehlich 3 (p = 0.04). When compared using the same soil/solution ratio, Mehlich 3 removed 4 to 8% more phosphorus than Bray 1. The soil/solution ratio used in the comparison affected the relationship between both extractants. The difference between extractants was slightly greater with a soil/solution ratio of 1:8 than of 1:10 (p = 0.03). Our results showed that even when using the same method, changes in the procedure (like soil/solution ratio) may cause different soil-test results and also differences in the relationship between two extracting solutions. Therefore, reported relationships between two methods are only valid for the soils and region where the relationship was developed and should not be extrapolated to other regions, even with similar soils. 相似文献
104.
本试验以新鲜沙棘果及奶酪为主要原料,探讨了沙棘再制奶酪的加工工艺。首先经护色、打浆、精磨、过滤、调酸、均质等工序,制备澄清均一的沙棘果汁。以样品感官品质和Vc含量为评价指标,通过单因素试验以及响应面试验,得出最佳配方及工艺为:35.00%天然奶酪、18.56%沙棘果汁(料水质量比1∶1)、1.54%复合乳化盐(m柠檬酸钠∶m多聚磷酸钠∶m焦磷酸钠∶m六偏磷酸钠=4∶2∶2∶1)、12.00%黄油、6.00%脱脂乳粉、6.00%白砂糖、0.50%复合稳定剂(m卡拉胶∶m黄原胶=4∶1),其余20.40%为纯净水,乳化温度为84 ℃,乳化时间为11.4 min,搅拌速度为3 000 r/min。经此工艺制成的成品,感官评分为57.5分(满分60分),Vc含量达16.61 mg/100 g。成品组织结构细腻光滑、色泽橘黄、口感润滑、营养丰富,具有沙棘果的风味,符合《GB25192—2010 再制奶酪》要求。 相似文献
105.
杂交构树叶多酚提取工艺优化及其抗氧化活性研究 总被引:1,自引:0,他引:1
为建立和优化杂交构树叶多酚的提取工艺,本试验采用超声波辅助提取的方法,以构树叶多酚得率为考察指标,通过单因素试验研究液料比、乙醇浓度、超声时间、超声温度4个因素对构树叶多酚得率的影响;在单因素试验的基础上,借助响应面法设计4因素3水平的试验方案,对构树叶多酚提取的工艺参数进行优化,建立回归模型并进行响应面分析,最终确定最佳的提取工艺参数,并进行3次平行验证;以维生素C为对照,通过测定构树叶多酚对DPPH和ABTS自由基的清除率,评价构树叶多酚的体外抗氧化活性。结果显示:4个因素对构树叶多酚得率的影响顺序依次为:乙醇浓度(B) > 液料比(A) > 超声温度(D) > 超声时间(C),响应面分析结果显示:两两因素之间存在交互作用,但交互作用不显著(P>0.05);在液料比为70:1、乙醇浓度为60%、超声时间为50 min、超声温度50 ℃的条件下,构树叶多酚的得率最大,为13.62 mg/g,与响应面法的预测值接近;体外抗氧化试验结果表明,构树叶多酚可以清除DPPH和ABTS自由基,并且在高浓度情况下可以达到与维生素C相当的水平。综上,试验建立的构树叶多酚提取工艺准确、可行,同时证明构树叶多酚具有良好的抗氧化活性;该结果可为构树叶多酚的生物活性研究以及构树叶的药用价值开发提供参考。 相似文献
106.
对灰铸铁的研究现状和生产中的一些新技术做了评述。重点介绍了高强度薄壁灰铸铁的生产现状以及先进的制造工艺和先进的制造手段在灰铸铁生产中应用所取得的技术成果。 相似文献
107.
XU Wan-yun WANG Hui-min WANG Wen-lun HU Meng-wei YAN Guo LI Jian-hua GAO Jian-feng 《中国畜牧兽医》2016,43(3):568-576
The specific primers were designed according to Ovis aries DRA gene sequence deposited in GenBank and the multiple cloning site of the plasmid pYD1,which was a vector used for protein surface display on Saccharomyces cerevisiae.The gene encoding DRA was amplified by PCR using the genomic RNA of Ovis aries.The 762 bp fragment was cloned and released in GenBank and registration number was KR422362.The PCR product was inserted into the yeast surface display plasmid vector pYD1 by double enzyme digestion.It was indicated that DRA gene was successfully integrated into the genome.Dot mutation was made at both ends of exon 2 in DRA gene for making restriction enzyme cutting site and design the exon 2 specific primers according to mutated Ovis aries DRA gene sequence.Sequenced exon 2 amplification products based on DNA pooling of sheep large sample template was analyzed the polymorphic loci.The polymorphic exon 2 246 bp fragment was obtained by double enzyme digestion and connected to surface display restructuring mutation carriers pYD1-DRA by the same double enzyme digestion,and then we successfully constructed yeast surface display libraries.We transformed it into Saccharomyces cerevisiae EBY100 cell.Yeast monoclone was identified by PCR amplification and sequencing,and we confirmed that DRA gene had been integrated into Saccharomyces cerevisiae genome.After galactose induced,it was detected that DRA gene library had been successfully demonstrated on the yeast cell surface under the fluorescence microscope by immunofluorescence method. 相似文献
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