2006～2007年世界塑料工业进展

收集了2006年7月～2007年6月世界塑料工业的相关资料,介绍了2006～2007年世界塑料工业的发展情况,提供了世界塑料产量、消费量及全球各类树脂的需求量及产能情况.按通用热塑性树脂(聚乙烯、聚丙烯、聚苯乙烯、聚氯乙烯、ABS树脂)、工程塑料(尼龙、聚碳酸酯、聚甲醛、热塑性聚酯、聚苯醚)、特种工程塑料(聚苯硫醚、液晶聚合物、聚醚醚酮)、通用热固性树脂(酚醛、聚氨酯、不饱和聚酯树脂、环氧树脂)不同品种的顺序,对树脂的产量、消费量、供需状况及合成工艺、产品应用开发、树脂品种的延伸及应用的进一步扩展等技术作了详细介绍.     

知识创新是工业尿素合成技术创新之本——实验室研究篇

对国内外研究者在尿素合成反应的热力学、动力学、化学平衡及相平衡等方面的研究成果进行了总结和评价,提供了尿素合成反应的热力学、动力学数据和相图,提出了一些新理念.     

意大利ES公司变频器进入中国市场

3月11日,"意科走进中国"新闻发布会在京举行,与来自冶金、石化、电力、建材、水处理、纺织、市政等行业的专家、用户及十几家业内知名的媒体共同分享了意科公司的发展历程,意科变频器的创新标准以及意科在奥运年全面推向中国市场的决心和计划.     

中国工程塑料市场综述(下)

4.3 聚碳酸酯海关进出口分析 1999～2006年间PC进口量年均增长27.91%,比1998～2005年间PC进口量年均增长率31.27%下降3.36个百分点.国内产量偏低、市场需求巨大的现状进一步暴露.中国PC消费主要依靠进口,2006年中国产量仅占总消费量的10%上下.1999～2006年间PC进口量年均增长27.91%,比1998～2005年间Pc进口量年均增长率36.68%下降3.36个百分点.2006年初级形状的聚碳酸酯进口地有45个,主要进口地为泰国(占16.49%),其次为中国(12.86%)、新加坡(11.50%)、美国(10.95%)、日本(10.65%)、韩国(9.81%)、中国台湾省(9.50%)、西班牙(7.46%),八进口地进口量占总进口量的89.2%.     

夹层粘接在大型机床导轨修理中的应用

1 "夹层粘接"新工艺 "夹层粘接"是作者经多年研究、开发的一种新技术,在设备大修理工作中,对于严重摩擦磨损的机床导轨,采用独特的"夹层粘接"工艺,以夹布塑料为加厚层,填充F4为表面耐磨层,使机床导轨恢复了原有的精度和尺寸要求,缩短了修理时间,减轻了劳动强度,节约了修理费用,取得了显著的综合效益.     

加压稀硝"三合一"主机修理小结

我公司年产80 kt加压稀硝装置是国内首例完全国产化装置,其"三合一"主机的汽轮机、减速机由杭汽制造,空压机、膨胀机由陕鼓生产.自1986年装置建成投运以来,每年检修都发现机组气封严重磨损,机壳与转子不同心.为此,公司利用2006年11月大修和2007年7月停车机会对机组进行了全面整修,以期从根本上消除存在的问题.     

工业评述2001～2002年国外塑料工业进展

收集了2001年7月到2002年6月有关国外塑料工业的相关期刊资料,介绍了2001年到2002年国外塑料工业的发展情况,提供了世界各地域塑料原材料的产量及构成比,日本、美国、加拿大、德国、法国、比利时、墨西哥、芬兰、西班牙等国家的树脂产量、消费量及增长率,以及日本、西欧、北美等地区的不同品种塑料原料消费量和增长率统计.按通用热塑性树脂(聚乙烯、聚丙烯、聚苯乙烯、聚氯乙烯、ABS树脂)、工程塑料(尼龙、聚碳酸酯、聚甲醛、热塑性聚酯、聚苯醚)、通用热固性树脂(酚醛、聚氨酯、不饱和树脂、环氧树脂)、特种工程塑料(聚苯硫醚、液晶聚合物、聚醚醚酮)不同品种的顺序,对树脂的产量、消费量及合成工艺、产品应用开发、树脂品种的延伸及应用的进一步扩展等有关技术作了详细的介绍.     

骨胶生产中蒸骨制胶操作方法

1 对蒸骨制胶过程的认识 蒸骨制胶的过程也就是用蒸汽使骨料块在密封的锅内受热、受压,使骨质疏松,由生胶质热解转变为可溶解于热水的动物胶质(习惯上称之为"骨胶")的过程.     

合成TBHQ的工艺改进

研究了以工业品甲基叔丁基醚(MTBE)和对苯二酚(HQ)为原料,在磷酸催化下,合成TBHQ的工艺参数.对催化剂的活性、原料的配比和反应时间等进行了优化考察.当对苯二酚∶甲基叔丁基醚∶磷酸=1∶1∶0.5(mol),反应温度为125℃,反应时间3.5h,TBHQ的收率达85.7%.与传统方法相比,该方法具有价廉、操作简单的特点,具有较高的开发、应用价值.用MTBE作原料合成TBHQ未见有关文献具体报道.     

湖光山色清新隽永——访江西省高级工艺美术师杨修勇

在我的办公桌上,放着一把<井岗山八角楼>粉彩山水壶,每当我空闲时,总喜欢拿在手中把玩,这件小小的山水壶虽不能展现气势豪雄的大写意山水画面,也不可能真正达到烟云满纸的效果,但细腻的工笔,雅静的画意给人一种清心的感觉和享受.     

硝酸分解磷矿生产饲钙、硝酸磷肥、硝酸钠的工艺技术

开发用硝酸分解磷矿制备饲料磷酸氢钙、工业硝酸钠及硝酸磷肥工艺,高效利用中低品位磷矿资源的技术,可将贵州丰富的磷、煤资源及国内的芒硝资源优势转化为产业优势,减少磷化工对硫资源的过度依赖,提高磷矿资源利用率,避免了磷石膏的排放,促进企业清洁生产,发展循环经济,实现可持续发展。     

Effect of phosphate,calcium, and pH on the dissolution of a phosphate rock in soil

The effect of phosphate (P), calcium (Ca), and pH on the dissolution of Sechura phosphate rock (SPR) in a Typic Dystrochrept was investigated in an incubation study over 90 days. Increasing the P status of the soil had little effect on either the rate or extent of dissolution of SPR, as measured by a single extraction with 0.5M NaOH, or on the amount of plant-available P in the soil as measured by the Bray procedure. This suggests that a reactive PR such as SPR could be effective as a maintenance P fertilizer on soils of medium and high P status.The dissolution of SPR at pH 6.4 was only 4% of total P added, compared to 33.6% of total P added at pH 5.2. Addition of Ca as CaCl₂, at the same rate of Ca as that added in Ca(OH)₂ to raise soil pH from 5.2 to 6.4, reduced the dissolution of SPR to 11% of total P added. The large effect of Ca on the dissolution of SPR contrasts with the small effect of soil P status and probably reflects the fact that the concentration of Ca in the soil solution is generally several orders of magnitude higher than that of P. The results obtained suggest that pH, per se, is of less importance in the dissolution and subsequent plant availability of P from phosphate rock in soil than previously thought.     

The effects of nitrogen fertilizer form on the plant availability of phosphate from soil,phosphate rock and mono-calcium phosphate

A glasshouse trial using lettuce as the test crop, and laboratory incubations were used to evaluate the influence of various nitrogen fertilizers on the availability of phosphate from an unfertilized loamy sand soil and from the same soil fertilized with Sechura phosphate rock or monocalcium phosphate. The order in which nitrogen fertilizer form increased plant yield and P uptake from soil alone and from soil fertilized with the rock was ammonium sulphate > sulphurised urea > ammonium nitrate > urea > potassium nitrate. For each rock application (both 30 and 60 mg/pot) and for soil alone, increased P uptake by the plant correlated well with decreased soil pH. In soil fertilized with the soluble P form, monocalcium phosphate, the form of the nitrogen fertilizer had little effect on plant P uptake. Subsequent laboratory incubation studies showed that increased dissolution of soil-P or Sechura phosphate rock did not occur until acidity, generated by nitrification or sulphur oxidation of the fertilizer materials, had lowered soil pH to below 5.5. A sequential phosphate fractionation procedure was used to show that in soils treated with the acidifying nitrogen fertilizers, ammonium sulphate and urea, there was considerable release of Sechura phosphate rock P to the soil, amounting to 42% and 27% of the original rock P added, respectively.     

The agronomic effectiveness of reactive rock phosphate,partially acidulated rock phosphate and monocalcium phosphate in soils of different pH

The initial and residual fertilizer effectiveness of North Carolina RP (rock phosphate), monocalcium phosphate and partially acidulated RP (made from North Carolina RP at 30% acidulation), both granulated and non-granulated, were measured in a glasshouse experiment. Triticale (xTriticosecale) was grown for 30 days on a soil that had been adjusted to three pH values (4.2, 5.2 and 6.2). Two crops were grown with a six month interval between crops. The effectiveness of the different fertilizers was compared using relationships between (1) yield of dried tops and the amount of P applied and (2) P content (P concentration in tissue multiplied by yield) and the amount of P applied. For the first crop, relative effectiveness (RE) of the fertilizers was calculated relative to granulated monocalcium phosphate, the most effective fertilizer. Monocalcium phosphate was not applied to the second crop, so relative residual effectiveness (RRE) was estimated for each fertilizer relative to the residual effectiveness of granulated monocalcium phosphate.The relative effectiveness of granulated monocalcium phosphate (band application) was greater (RE = 1.00) than of North Carolina RP (0.01–0.02) and partially acidulated RP (0.45–0.76) for all three soil pH values for the first crop. Granulation and band application increased the effectiveness of monocalcium phosphate and partially acidulated RP, but reduced the effectiveness of North Carolina RP. Both non-granulated monocalcium phosphate and partially acidulated RP were less effective than granulated partially acidulated RP for both crops. For the second crop granulated monocalcium phosphate was most effective and the RRE of non-granulated partially acidulated RP (0.16–0.32) and North Carolina RP (0.19–0.28) was greater than for non-granulated monocalcium phosphate (0.12). For the more acidic soil the RE of non-granulated North Carolina RP was four times higher than for the high pH soil for the first crop and 60% higher for the second crop, but it was still poorly effective relative to granulated monocalcium phosphate. Granulated North Carolina RP was least effective among all the fertilizers for all soil pH values and for both crops.     

湖北远安磷矿成分分析及磷富集实验

以市售湖北特大磷矿区内远安县荷花镇品位较低的磷矿为样本,分析了该磷矿石的成分,得出该磷矿石中各主要成分的质量分数为:P<,2>O<,5> 24.04%,CaO 49.17%,Fe<,2>O<,3> 1.49%,Al<,2>O<,3> 1.95%,MgO 3.22%,SiO<,2> 7.32%.基于此数据,本文采用了稀硫...     

Agronomy,modelling and economics of reactive phosphate rocks as slow-release phosphate fertilizers for grasslands

Reactive phosphate rocks (RPRs) from Sechura, Peru (SPR) and North Carolina, USA (NCPR) were compared with triple superphosphate (TSP) as phosphate (P) fertilizers for permanent grass/clover pastures in four field trials in New Zealand. Trial sites ranged in initial pH (in water) from 5.7 to 6.3 and in rainfall from 712 to 1338 mm yr^–1. SPR and NCPR were used in the unground as-received state. Fertilizers were applied annually for six years. Pasture was harvested by frequent mowing, and herbage dry matter (DM) yields were measured at each cut. Herbage P concentrations were measured at each cut in two trials and on most cuts in the other two.For all sites combined, DM production from RPRs was initially significantly less than from TSP but it improved relative to TSP with time. Substitution values of RPR relative to TSP, denoted by S.V. (TSP/RPR) and defined as the ratio of P in TSP to P in RPR required to produce the same plant response during a specified period of time, were estimated by relating yields from RPR treatments to the yield response curve for different application rates of TSP. For the four trials combined, S.V. (TSP/SPR) increased from 0.32 in year 2 to 0.85 in year 6. S.V. values for NCPR were similar. The site which had the lowest S.V. values (average 0.20) for total production over six years was the site with highest pH (6.3) and lowest rainfall (712 mm). Corresponding S.V. values for the other sites were 0.50 to 0.78.Herbage P concentrations showed a similar pattern of RPR performance relative to TSP to that shown by DM production except at the highest application rate where TSP always supported much higher herbage P concentrations than RPR.The pattern of DM production from RPR relative to TSP was explained on the basis of a model involving soil P pools of undissolved fertilizer P and plant-available P respectively, with the hypothesis that P dissolved from RPR entered the plant-available P pool and was used with the same efficiency as P entering by dissolution of TSP. Model predictions of substitution values using directly measured RPR dissolution rates agreed well with observed substitution values.The advantage of RPRs in comparison to soluble P fertilizers for permanent pastures was considered to lie in their lower price and not in greater nutrient efficiency. Economic advantage was calculated in terms of the return on investment from establishing and maintaining a pool of RPR in the soil large enough to release the required annual amount of plant-available P compared with the cost of annual applications of soluble P fertilizer.     

间苯二酚-双[二(季戊四醇)]磷酸酯的合成、表征和热稳定性

采用季戊四醇、三氯氧磷和间苯二酚为反应物,合成了新型添加型阻燃剂:间苯二酚-双[二(季戊四醇)]磷酸酯(RBPP),通过元素分析、FTIR和1HNMR等测试技术表征了标题化合物的结构,结果表明,所合成的标题化合物的结构与预期的结构一致.热失重分析结果证明,RBPP质量损失5%时的温度在350.0℃,600℃残炭率高达5...     

利用磷矿制备饲料添加剂磷酸二氢钙

以磷矿为原料制备磷酸,通过化学沉淀法脱氟除杂质得到净化的磷酸,再将净化后的磷酸与碳酸钙反应制备饲料级磷酸二氢钙.考察了硫酸质量分数、石灰乳用量、反应时间和反应温度4个因素对磷酸二氢钙产率的影响,得到了制备磷酸二氢钙的最佳工艺条件:硫酸质量分数60％,石灰乳用量7.00 g,反应时间1.5h,反应温度50℃.在此最佳工艺...     

Preparation,forms and properties of controlled-release phosphate fertilizers

Controlled-release phosphate fertilizers include phosphate rocks (PRs) for direct application, partially acidulated phosphate rocks (PAPRs) and thermal phosphates. Phosphate rocks contain apatite as the main P containing mineral, the composition and the chemical nature of which vary between PRs. Based on the solubility in chemical extractants PRs are broadly grouped into ‘reactive’ and ‘unreactive’. The ‘reactivity’ of PRs is influenced strongly by the extent of carbonate substitution for phosphate in the apatite minerals. Under certain soil and climatic conditions reactive PRs (RPRs) can be used as a source of P for direct application. Partially acidulated phosphate rocks (PAPRs) are produced either by direct partial acidulation of PRs with mineral acids or by mixing PRs with fully acidulated superphosphate reaction mixtures. Partial acidulation of PRs with H₃PO₄ generally results in higher water soluble P contents than those acidulated with H₂SO₄. Mixing of RPRs with superphosphate reaction mixtures sometimes results in the preferential consumption of free acid and thereby increases the amounts of residual unreacted PRs. Thermal phosphates are produced by either heating PRs below melting point both in the presence and the absence of silica (calcined phosphates) or heating PRs with silica above melting point (fused phosphate). These phosphates are alkaline in nature and hence suitable for acidic soils.     

A novel lanthanum-modified bentonite,Phoslock, for phosphate removal from wastewaters

Phoslock^®, a lanthanum-modified bentonite, has been investigated for phosphate uptake from synthetic and real wastewaters in laboratory and field. In laboratory tests, equilibrium and kinetics were studied at various temperatures, ionic strength, and pHs. The investigation indicated that phosphate adsorption occurs through a chemisorption process. The activation energy of the adsorption process was calculated based on pseudo-second order rate constant. The maximum adsorption capacity of Phoslock was unaffected at pH 5–7, but decreased at higher pHs. The monovalent phosphate anion, H₂PO₄⁻, had the greatest affinity for the adsorbent surface. Furthermore, it was also shown that the activation energy was lower at a higher solution pH attributed to the loss of adsorption sites at the higher pHs while it remained unaffected by the ionic strength of the solution. A field test also demonstrated that the Phoslock works well for phosphate uptake in polluted waters.