Predicting external sulphur requirement of alfalfa from sulphate sorption isotherm of Tanzanian soils

For Tanzanian soils dominant in hydrous oxides of iron and amorphous ferri-alumino silicate, a 48-hour (hr) mixing period with the sulphate (SO₄) solution was adequate for a near-equilibrium condition. Although differing in their SO₄ sorption capacity, all the soils sorbed SO₄ at or beyond 1µg ml^–1 sulphur (S) concentration in the supernatant. Hydroxyl (OH) ions were displaced during SO₄ sorption as indicated by a significant positive correlation between the amount of sorbed SO₄ and the difference in pH values determined in 0.1N K₂ SO₄ and 0.1N KCl, i.e. the dpH values.In a greenhouse experiment, alfalfa was grown on eight soils at six adjusted S concentrations. Sulphur deficiency symptoms appeared in the control pots of those soils which were low in native sorbed SO₄, SO₄ sorption capacity and initial soil solution S concentration. Sulphur fertilization increased dry matter (DM) yield as well as response to applied S. The external S concentration, i.e. adjusted S concentration required for 95% of the maximum DM yield, ranged from 0.8 to 8.2µg S ml^–1 with values less than 2.0 on most of the soils. The external S concentration decreased hyperbolically as the SO₄ sorption capacity of the soils increased. The total amount of fertilizer S required to obtain the external S concentration in solution, and at the same time satisfy the SO₄ sorption capacity of the soil at the external S concentration (determined from the sorption isotherm) was defined as the external S requirement for the specified yield level of alfalfa. The external S requirement for 95% of the maximum yield of alfalfa varied from soil to soil due to differences in their capacity and intensity for S nutrition.Part of a thesis by the senior author for the MSc (Agric) degree of the University of Dar es Salaam     

Surface tension and contact angle of herbicide solutions affected by surfactants

Contact angle and surface tension were measured for distilled and hard water solutions of adjuvants, Ortho X-77, Span-20, Sterox-NJ. Surfactant-WK, Triton B-1956, Triton X-114, Tween-20, and Sun Oil 11E. The same parameters were measured for suspensions of atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine] and ametryne [2-(ethylamino)-4-(isopropylamino)-6-(methylthio)-s-triazine] with and without each adjuvant. All adjuvants reduced surface tension and contact angle of distilled water; Surfactant-WK was most effective and Tween-20 was least effective. Increasing concentration of surfactants from 0 to 0.1% (v/v) gave progressive reduction in surface tension and contact angle while higher concentrations, 0.1 to 2.0% (v/v), had no further effect. Surfactant-WK at 0.1% (v/v) in distilled water reduced the surfact tension from 72.8 dynes/cm to 27 dynes/cm and contact angle from 110° to 41°. An additional increase in Surfactant-WK concentration from 0.1% (v/v) to 2% (v/v) did not further reduce surface tension and contact angle. Sun Oil 11E was identical in behavior except that it was less effective than the surfactants. Water hardness up to 1,000 ppm as Ca ions did not affect surface tension and contact angle in surfactant solutions. An aqueous solution of atrazine had a higher surface tension and contact angle than ametryne in the absence of surfactants. However, these differences were not observed when surfactants were added to either herbicide.     

Lime-induced iron chlorosis in sugarcane

Lime-induced chlorosis is a potential problem on most calcareous soils particularly in arid and semi-arid climates affecting most of the plants grown on them. Bicarbonates, phosphates, calcium, iron inactivation in plant tissue and organic anions have been held responsible as the mechanism leading to the disorder which is still not fully understood, and there is a lack of agreement as to the primary factor responsible for lime-induced chlorosis. To date, no hypothesis has adequately explained why chlorosis occurs on some high lime soils and not on others. Likewise, the nutrient ratios, K/Ca, P/Fe and Fe/Mn considered as diagnostic criteria for lime-induced chlorosis, have shown inconsistency. The presence of calcium carbonate, bicarbonate, calcium and imbalance of nutrient cations in the growth medium, injudicious addition of phosphates, quality of irrigation water, and other soil and plant factors have been held responsible for the disorder. Amelioration of lime-induced chlorosis by (i) acidification of calcareous soils, (ii) use of iron salts, (iii) use of synthetic iron chelates, and (iv) by management practices including the selection and development of varieties resistant to lime-induced iron chlorosis, is discussed. Suggestions for future research work are made.     

Formation of Nanocrystalline Calcia by the Decomposition of Calcite

Formation of nanocrystalline calcia from calcite has been studied in situ via transmission electron microscopy. The crystallographic transformation occurred via two mechanisms: the first is by distortion of the cleaved rhombohedron of calcite, formed by {104} planes in hexagonal coordinates, into a cube. This produced a microstructure of oriented, elongated nanocrystals of calcia with planar boundaries. In the second mechanism, the micrometer-sized parent calcite particles broke up into nano-sized grains as the decomposition began, leading to irregularly shaped, randomly oriented nanocrystals of calcia.     

Studies on chemical resistance of polyesters

Chlorendic anhydride based polyester ( I ,) tetrachlorophthalic anhydride based polyester ( II ), dibromoneopentyl glycol based polyester ( III ,) general purpose polyester ( IV ,) blend of dibromoneopentyl glycol based polyester with general purpose polyester ( V ,) chlorendic anhydride and dibromoneopentyl glycol based polyester ( VI ), and a blend of chlorendic anhydride based polyester and dibromoneopentyl glycol based polyester ( VII ) were prepared and their chemical resistance and moisture absorption studied in various reagents, acid, alkali, and water, at 25 and 65°C. It is found that the polyester ( III ) is the least affected in the presence of the acids. In 20% NaOH, there was a decrease in weight for all polyesters at both the temperatures compared to the control except the polyester ( VII ). Increase in weight of all the polyesters was observed during the absorption of moisture both at 25 and 65°C. The increase was higher at higher temperature. Polyester ( III ) thus shows the least absorption of moisture.     

Thermal stability of PVC/chlororubber-20-graft polyblend–styrene–acrylonitrile blends. I

Thermal stability of PVC blends with chlororubber-20-graft polyblend-styrene-acrylonitrile [CR-20gp-SAN (2:1)] was studied by HCI evolution techniques and thermogravimetry under isothermal condition. The thermal stability of PVC/CR-20gp-SAN (2:1) blends has been compared with those of PVC/CR-20 and PVC/KM-365B blends. It has been observed that the thermal stability of modified PVC is less than that of unmodified PVC. The CR-20gp-SAN (2:1) modified PVC blends were found to be more stable than PVC/CR-20 blends but less stable than PVC/KM-365B blends. The rate of degradation in PVC blends were observed to be unaffected by the concentration of the modifiers, but the PVC/KM-365B blends were found to be degrading slower in comparison with PVC/CR-20 and PVC/CR-20gp-SAN (2:1) blends. The rate of degradation for PVC/CR-20 blends at lower concentrations (<10%) of modifiers is almost equal to that of PVC/CR-20-gp-SAN (2:1) blends, but more at higher concentrations of modifiers (>10%). The experimental results have been explained on the basis of the chemical nature of the modifiers and their miscibility with PVC.     

Note: The Use of Triallyl Cyanurate in Bonding PVC Plastisols to Steel

The use of diallyl phthalate as the basis for a non-extractable plasticizer for poly(vinylchloride) (PVC) is well-known. Used in conjunction with a primary plasticizer and a polymerization initiator, a plastisol coating for steel can be formulated which is oil or grease tolerant and can also be used for bonding some structural steel parts if the area is relatively large compared with the load to be applied. Defrayne and Twiss¹ describe the bonding of automobile hood assemblies by vinyl plastisol adhesives and Schneberger² emphasizes their use in the automobile industry though neither article gives the formulations employed. Commercial formulations giving pull-off strengths of the order of 1 to 4 MN. m^-2 always incorporate a proportion of a phenolformaldehyde resin or even an epoxy, but sound-deadening and other coatings of steel do not necessarily need this reinforcement. Phillips and Longworth³ particularly studied the use of diallylphthalate (DAP) as a polymerizable plasticizer and the consequent improvement in adhesion to mild steel. Sherlock⁴ used a simple formulation without additives when investigating the effect of surface cleaning and conversion coatings (oxides and phosphates). It was suggested that, as outlined below, improved adhesion would be expected if a small proportion of triallyl cyanurate (TAC) were added to the polymerizable plasticizer. This paper shows this expectation to be achieved although the proportion of the more expensive TAC needed for substantial increase in bond strength is greater than was hoped.     

Liver disorder detection using variable- neighbor weighted fuzzy K nearest neighbor approach

The human liver disorder is a genetic problem due to the habituality of alcohol or effect by the virus. It can lead to liver failure or liver cancer, if not been detected in initial stage. The aim of the proposed method is to detect the liver disorder in initial stage using liver function test dataset. The problem with many real-world datasets including liver disease diagnosis data is class imbalanced. The word imbalance refers to the conditions that the number of observations belongs to one class having more or less than the other class(es). Traditional K- Nearest Neighbor (KNN) or Fuzzy KNN classifier does not work well on the imbalanced dataset because they treat the neighbor equally. The weighted variant of Fuzzy KNN assign a large weight for the neighbor belongs to the minority class data and relatively small weight for the neighbor belongs to the majority class to resolve the issues with data imbalance. In this paper, Variable- Neighbor Weighted Fuzzy K Nearest Neighbor Approach (Variable-NWFKNN) is proposed, which is an improved variant of Fuzzy-NWKNN. The proposed Variable-NWFKNN method is implemented on three real-world imbalance liver function test datasets BUPA, ILPD from UCI and MPRLPD. The Variable-NWFKNN is compared with existing NWKNN and Fuzzy-NWKKNN methods and found accuracy 73.91% (BUPA Dataset), 77.59% (ILPD Dataset) and 87.01% (MPRLPD Dataset). Further, TL_RUS method is used for preprocessing and it improved the accuracy as 78.46% (BUPA Dataset), 78.46% (ILPD Dataset) and 95.79% (MPRLPD Dataset).

     

高速公路施工区车辆强制换道耗时生存模型

为研究高速公路施工区车辆强制换道行为及其影响因素,采用生存分析中的半参数分析方法建立强制换道耗时的乘法风险率模型.通过无人机拍摄采集高速公路施工区的车辆换道耗时及其影响因素数据,最终确立换道耗时Cox比例风险模型,对换道耗时数据进行Cox回归建模分析.结果表明:近77%的换道车辆在10 s内完成换道;小型车和中型车经养护施工区的换道耗时未发现显著性差别;对于相同的换道耗时,平峰期的累积生存率明显低于高峰期和过渡时期,而高峰期的累积生存率最高.建立的强制换道耗时生存模型可有效的定量分析车型和交通时段对高速公路施工区车辆换道行为的影响,可为高速公路施工区交通管理控制及车辆换道行为建模及仿真奠定一定的理论基础.     

Oxidation behavior of 2.25Cr-1Mo steel with prior tempering at different temperatures

The oxidation behavior of a normalized 2.25Cr-1Mo steel tempered previously for 10 hr at different temperatures between 873 and 1023 K has been studied up to a maximum duration of 1000 hr in air at 773–973 K. The oxidation resistance of the steel was found to decrease significantly with the temperature of tempering. Tempering of this steel is reported to cause microstructural changes involving precipitation of Cr as carbides and a decrease in the effective (free) Cr contents, that could influence the oxidation resistance of the Cr-containing alloys. Relative compositions across the thickness of the oxide scales, as analyzed by SEM/EDX and SIMS, suggest that a less Cr-rich (and less protective) and thicker scale on the steel formed because previous tempering caused extensive depletion of free Cr.