Crop residue,manure and fertilizer in dryland maize under reduced tillage in northern China: I grain yields and nutrient use efficiencies

The rapidly increasing population and associated quest for food and feed in China has led to increased soil cultivation and nitrogen (N) fertilizer use, and as a consequence to increased wind erosion and unbalanced crop nutrition. In the study presented here, we explored the long-term effects of various combinations of maize stover, cattle manure and nitrogen (N) and phosphorus (P) fertilizer applications on maize (Zea mays L.) yield and nutrient and water use efficiencies under reduced tillage practices. In a companion paper, we present the effects on nutrient balances and soil fertility characteristics. The ongoing factorial field trial was conducted at Shouyang Dryland Farming Experimental Station in northern China from 1993 onwards. The incomplete, determinant-optimal design comprised 12 treatments, including a control treatment, in duplicate. Grain yields and N, P, and potassium (K) uptakes and N, P and K use efficiencies were greatly influenced by the amount of rain during the growing season (GSR), and by soil water at sowing (SWS). There were highly significant interactions between GSR and added stover and manure, expressed in complex annual variations in grain yield and N, P and K use efficiencies. Annual mean grain yields ranged from 3,000 kg ha⁻¹ to 10,000 kg ha⁻¹ and treatment mean yields from 4,500 kg ha⁻¹ to 7,000 kg ha⁻¹. Balanced combination of stover (3,000–6,000 kg), manure (1,500–6,000 kg) and N fertilizer (105 kg) gave the highest yield. Stover and manure were important for supplying K, but the effects differed greatly between years. Overall mean N recovery efficiency (NRE) ranged from 28% to 54%, depending on N source. NRE in wet years ranged from 50% to 90%. In conclusion, balanced combinations of stover, manure and NP fertilizer gave the highest yield and NRE. Reduced tillage with adding stover and manure in autumn prior to ploughing is effective in minimizing labor requirement and wind erosion. The potentials of split applications of N fertilizer, targeted to the need of the growing crop (response farming), should be explored to further increase the N use efficiency.     

氯化钾镀锌液中各组份对镀液性能的影响

通过三位级正交试验法,讨论了镀锌液中各类添加剂的性能;抗杂质干扰能力;氯化锌与其它镀锌溶液性能比较以及其它镀锌怎样转化为氯化锌镀锌液。     

Comparing sensitivities of differently oriented multi-walled carbon nanotubes integrated on silicon wafer for electrochemical biosensors

In this study, we report on multi-walled carbon nanotubes fabricated on silicon substrate with four different orientations via chemical vapor deposition. It is well-known that chemical treatments improve the nanotube electrochemical reactivity by creating edge-like defects on their exposed sidewalls. Before use, we performed an acid treatment on carbon nanotubes. To prove the effect of the treatment on these nanostructured electrodes, contact angles were measured. Then, sensitivities and detection limits were evaluated performing cyclic voltammetry. Two target molecules were used: potassium ferricyanide, an inorganic electroactive molecule, and hydrogen peroxide that is a product of reactions catalyzed by many enzymes, such as oxidases and peroxidases. Carbon nanotubes with tilted tips become hydrophilic after the treatment showing a contact angle of 22° ± 2°. This kind of electrode has shown also the best electrochemical performance. Sensitivity and detection limit values are 110.0 ± 0.5 μA/(mM cm²) and 8 μM for potassium ferricyanide solutions and 16.4 ± 0.1 μA/(mM cm²) and 24 μM using hydrogen peroxide as target compound. Considering the results of wettability and voltammetric measurements, nanotubes with tilted tips-based electrodes are found to be the most promising for future biosensing applications.     

A dual K-Na selective Prussian blue nanotubes sensor

A strategy for dual sensing of Na⁺ and K⁺ ions using Prussian blue nanotubes via selective inter/deintercalation of K⁺ ion and competitive inhibition by Na⁺ ion, is reported. The analytical signal is derived from the cyclic voltammetry cathodic peak position E_pc of Prussian blue nanotubes. Na⁺ and K⁺ levels in a sample solution can be determined conveniently using one Prussian blue nanotubes sensor. In addition, this versatile method can be applied for the analysis of single type of either Na⁺ or K⁺ ions. The dual-ion sensor response towards Na⁺ and K⁺ can be described using a model based on the competitive inhibition effects of Na⁺ on K⁺ inter/deintercalation in Prussian blue nanotubes. Successful application of the Prussian blue nanotubes sensor for Na⁺ and K⁺ determination is demonstrated in artificial saliva.     

Potassium catalysis in the pyrolysis behaviour of short rotation willow coppice

Short rotation willow coppice (SRC) and a synthetic biomass, a mixture of the basic biomass components (cellulose, hemicellulose and lignin), have been investigated for the influence of potassium on their pyrolysis behaviours. The willow sample was pre-treated to remove salts and metals by hydrochloric acid, and this demineralised sample was impregnated with potassium. The same type of pre-treatment was applied to components of the synthetic biomass. Characterisation was performed using thermogravimetric analysis with measurement of products by means of Fourier transform infrared spectroscopy (TGA-FTIR) and pyrolysis-gas chromatography-mass spectrometry (PY-GC-MS). A comparison of product distributions and kinetics are reported. While the general features of decomposition of SRC are described well by an additive behaviour of the individual components, there are some differences in the magnitude of the influence of potassium, and on the products produced. For both SRC and the synthetic biomass, TGA traces indicate catalytic promotion of both of the two-stages of biomass decomposition, and potassium can lower the average apparent first-order activation energy for pyrolysis by up to 50 kJ/mol. For both SRC and synthetic biomass the yields and distribution of pyrolysis products have been influenced by the presence of the catalyst. Potassium catalysed pyrolysis increases the char yields markedly and this is more pronounced for synthetic biomass than SRC. Gas evolution profiles during pyrolysis show the same general features for both SRC and synthetic biomass. Relative methane yields increase during the char formation stage of pyrolysis of the potassium doped samples. The evolution profiles of acetic acid and formaldehyde change, and these products are seen in lower relative amounts for both the demineralised samples. A greater variation in pyrolysis products is observed from the treated SRC samples compared to the different synthetic biomass samples. Furthermore, substituted phenols from lignin pyrolysis are more dominant in the pyrolysis profiles of the synthetic biomass than of the SRC, implying that the extracted lignins used in the synthetic biomass yield a greater fraction of monomeric type species than the lignocellulosic cell wall material of SRC. For both types of samples, PY-GS-MS analyses show that potassium has a significant influence on cellulose decomposition markers, not just on the formation of levoglucosan, but also other species from the non-catalysed mechanism, such as 3,4-dihydroxy-3-cyclobutene-1,2-dione.     

微波消解法快速测定废水中的总磷

采用微波对废水中的总磷进行消解,考察了消解时间、功率等不同实验条件对标样微波消解的影响,得出本实验消解的最佳条件,即过硫酸钾溶液用量为 0.5 mL,压力为10 MPa,消解时间为 2 min：并将该法与总磷测定的常规方法进行了比较,结果表明,过硫酸钾-微波消解法操作简单,效率高,对工作环境污染小.最后对微波消解法的精密度和准确度进行验证,实验结果表明其具有良好的精密度和准确度.     

铝酸钠(钾)溶液种分过程的粒度研究

采用间歇式反应器,研究了52 5℃,COH-=5 16mol/L,αk分别为1 45、1 55、1 65的纯铝酸钠和铝酸钾溶液种分过程的晶体粒度分布(PSD)规律。结果表明,在相同的分解条件下,铝酸钠和铝酸钾溶液中晶体的粒度分布随时间的变化有一定差异。铝酸钠溶液PSD曲线的主粒度峰的位置总在铝酸钾溶液的上方;最显著的差异是在分解16h后,铝酸钾溶液的PSD曲线在10～44 774μm处有一个显著的突起峰,而铝酸钠溶液则没有。不同αk的铝酸钠和铝酸钾溶液,这种粒度分布随时间变化的差异相似。     

Effects of the central potassium ions on the G-quadruplex and stabilizer binding

Human telomeres undertake the structure of intra-molecular parallel G-quadruplex in the presence of K⁺ in eukaryotic cell. Stabilization of the telomere G-quadruplex represents a potential strategy to prevent telomere lengthening by telomerase in cancer therapy. Current work demonstrates that the binding of central K⁺ with the parallel G-quadruplex is a coordinated water directed step-wise process. The K⁺ above the top G-tetrad is prone to leak into environment and the 5′-adenine quickly flips over the top G-tetrad, leading to the bottom gate of G-tetrads as the only viable pathway of K⁺ binding. Present molecular dynamics studies on the two most potent stabilizers RHPS4 and BRACO-19 reveal that the central K⁺ has little influence on the binding conformations of the bound stabilizers. But without the central K⁺, either RHPS4 or BRACO-19 cannot stabilize the structure of G-quadruplex. The binding strength of stabilizers evaluated by the MM-PBSA method follows the order of BRACO-19> RHPS4, which agrees with the experimental results. The difference in binding affinities between RHPS4 and BRACO-19 is probably related to the ability to form intramolecular hydrogen bonds and favorable van del Waals interactions with G-quadruplex. In the models that have one central K⁺ located at the upper/lower binding site, the corresponding top/bottom stacked stabilizers show more favorable binding affinities, indicating the apparent promoting effect of central K⁺ on the stabilizer binding. Our findings provide further insights into the regulatory effect of K⁺ on the G-quadruplex targeted binding, which is meaningful to the development of G-quadruplex stabilizers.     

Benign and efficient preparation of thioethers by solvent-free S-alkylation of thiols with alkyl halides catalyzed by potassium fluoride on alumina

The preparation of thioethers by S-alkylation of various thiols with alkyl halides under solvent-free reaction conditions using potassium fluoride on alumina (KF/Al₂O₃) as a solid catalyst has been investigated in detail with respect to three different modes of reaction activation (ultrasound irradiation, microwave irradiation, and conventional heating) for obtaining maximum yield of the thioether. The importance of KF/Al₂O₃ as a particularly efficient catalyst was corroborated for all three modes of reaction activation, although the reaction time was found to be strongly dependent on the mode of activation. The yield of the thioethers was also found to depend on the amount of the solid catalyst relative to the equimolar amounts of the two reactants.     

Controlled oxidation-reduction potential on dark fermentative hydrogen production from glycerol: Impacts on metabolic pathways and microbial diversity of an acidogenic sludge

The oxidation-reduction potential (ORP) is an important factor in H₂ production via dark fermentation however its effect over microbial diversity in an acidogenic sludge has not, been well studied. This work studies the effect of ORP controlled by hydrogen peroxide and potassium ferricyanide on continuous hydrogen production and microbial diversity in an acidogenic sludge fed (HRT 12 h and pH 5.5) with glycerol. Results show that the more oxidizing ORP control environment (?540 mV) improves H₂ yield by 50–70% (0.31–0.51 molH₂/mol glycerol) over non-ORP control conditions. Oxidizing ORP values were shown to enrich microorganisms of the genus Clostridium, which have been linked to high H₂ yields. Therefore, controlling ORP in an acidogenic sludge was shown to directly modify microbial diversity at the genus level, and could likely to indirectly regulate metabolic function. Additionally, metabolic pathways were regulated by the kind of agent used.