PEI/APP改性脲醛树脂制备阻燃胶合板及性能

以聚乙烯亚胺(PEI)为改性剂处理聚磷酸铵(APP)制备得到APP@PEI阻燃体系,并将其加入到脲醛树脂(UF)中,制备阻燃胶合板。研究了APP@PEI对UF胶黏剂理化性能的影响,并进一步探讨其对胶合性能及阻燃性能的影响。结果表明:APP、PEI和APP@PEI对UF的黏度、pH和固化时间均有影响。当APP添加量为10%时,UF的黏度由3.843 Pa·s上升至8.270 Pa·s,pH降至5.67,固化时间由91 s降至87 s;当PEI添加量为0.91%时,由于UF体系中支化和交联程度增加,黏度上升至41.433 Pa·s,pH和固化时间分别提升至9.91和116.3 s;而APP@PEI能降低对UF各项性能的影响,添加10%APP@PEI时UF的黏度、pH和固化时间分别为5.966 Pa·s、6.33和94.3 s。添加APP后,胶合板的胶合强度均低于Ⅱ类胶合板强度标准(0.7 MPa);添加PEI后,胶合板的胶合强度能够提升18%以上;APP@PEI添加量为10%时,胶合板的胶合强度达0.85 MPa,高于Ⅱ类胶合板强度标准要求。添加APP、PEI和APP@PEI对胶合板的阻燃性能有不同影响,单独添加PEI无法改善胶合板的阻燃性能,当APP和APP@PEI添加量为10%,15%和20%时,胶合板的极限氧指数(LOI)分别比未添加阻燃剂时提高0.8%,2.0%,2.5%和1.2%,2.2%,3.1%。     

Inhibiting fungus on largemouth bass eggs with copper sulfate and its toxicity to fry and juveniles

This study determined the effectiveness of copper sulfate (CuSO₄) to inhibit fungal growth (caused by Saprolegnia spp.) on largemouth bass (LMB) eggs spawned on/in fiber mats in very high-alkalinity/-hardness waters; experiments also determined the toxicity of CuSO₄ to LMB fry and juveniles. An untreated control and three CuSO₄ concentrations (10, 20, and 40 mg/L) were tested under a flow-through scenario in the effectiveness experiment. Eggs were treated daily until hatching began. Fungal load at the time of hatch had a total area > 3.0 cm² in the untreated controls, total area 1.0 to <2.0 cm² in the 10 and 20 mg/L CuSO₄ treatments, and total area > 1.0 cm² in the 40 mg/L CuSO₄ treatments. Fungus samples were identified as Saprolegnia australis. The 24-hr median lethal concentration (LC50) values on the LMB yolk-sac and swim-up fry were 32.0 and 4.6 mg/L CuSO₄, respectively; the No Observed Effect Concentrations (NOEC) were 16.0 and 0.125 mg/L CuSO₄, respectively. Juvenile LMB were extremely tolerant to CuSO₄, and their 24-hr LC50 value was 185.5 mg/L; the NOEC was 64 mg/L. This study indicates that CuSO₄ can be an important resource for hatcheries to control egg fungus, especially in high-alkalinity/-hardness waters.     

FeSO4引发提高秦艽种子萌发的生理机制

为探讨FeSO4引发提高秦艽种子萌发抗性的生理机制,同时设置水引发处理,以未作任何处理的种子为对照(CK),研究了0.6%FeSO4引发处理24 h对种子膜透性、储藏性物质、能量、激素及抗性相关酶等方面的影响。结果表明:FeSO4引发降低了种子膜透性,提高种子活力,在吸水12 h和24 h时,电导率分别较CK降低了6.61%和11.67%;调动了种子内部储藏物质的代谢,蔗糖含量减少9.57%,可溶性蛋白增加49.63%,饱和脂肪酸中的豆蔻酸和木焦油酸甲酯含量分别增加4.93%和9.03%,不饱和脂肪酸中的山嵛酸、油酸、亚油酸和亚麻酸分别减少6.73%、8.18%、8.40%和6.70%;改变了种子激素平衡,其中脱落酸的含量下降64.78%,赤霉素含量增加近22倍;加速了种子能量代谢, ATP含量增加2.16倍,细胞色素C氧化酶活性增加67.91%。此外,FeSO4引发使线粒体非酶促系统中谷胱甘肽含量和抗坏血酸的含量分别增加74.08%和10.89%,使细胞内酶促系统超氧化物歧化酶、过氧化氢酶和抗坏血酸过氧化物酶活性分别增加285%、179%以及19.6%。因此,FeSO4引发对种子萌发是一个综合过程,一方面可促进种子物质代谢和提高能荷水平,一方面可改善种子内部生理状态和提高胁迫响应能力,从而提高种子活力,促进种子快速和整齐萌发。     

华北玉米农田大气/植被界面氨气和铵盐动态变化研究

为系统研究大气/植被界面还原性氮(氨气和铵盐,NHx)的动态变化,选择华北典型玉米农田生态系统,于2016年8月和9月开展了2次综合观测实验,同步采集并测量了植被冠层大气中氨气和铵盐浓度(气溶胶和降水)、玉米叶片和土壤中铵盐含量。结果表明:实验期间(玉米抽穗期和花粒期),植被冠层氨气和铵盐浓度的平均值分别为30.6±6.8μg·m~(-3)和5.9±3.3μg·m~(-3),变化范围分别为21.1~37.6μg·m~(-3)和2.1~8.0μg·m~(-3);降水过程造成植被冠层的气溶胶铵盐浓度下降了75%,这一比例(被降水湿清除的效率)显著高于氨气。玉米叶片中铵盐含量从植株顶端到底部呈现下降趋势,变化范围为0.17~0.25 mg·g~(-1)(抽穗期)和0.74~1.20 mg·g~(-1)(花粒期),且呈现随温度升高而升高的日变化特征。抽穗期植株氨气补偿点为1.9±1.4μg·m~(-3),远低于大气氨气浓度31.4±4.8μg·m~(-3);花粒期植株氨气补偿点52.0±30.7μg·m~(-3),高于大气氨气浓度29.3±11.7μg·m~(-3)。8月10—13日玉米抽穗期,大气活性氮通过降水、气体和气溶胶3种途径输入到农田的总量约25 mg N·m~(-2)·d~(-1),是农田土壤和作物可利用氮的重要来源。农田氮管理中需要充分考虑植被与冠层大气氨的交换过程。     

不同原料生物炭对铵态氮的吸附性能研究

为探讨不同原料生物炭对铵态氮吸附量及吸附机制,以花生壳、玉米秆、杨木屑和竹屑为原料,在500℃下充N_2保护热解制备生物炭,通过电镜扫面图(SEM)与傅立叶红外光谱图(FTIR)表征NH_4~+-N在生物炭表面的吸附特征,结合批量平衡吸附试验,对比研究不同原料生物炭对NH_4~+-N的吸附性能。结果表明:吸附后生物炭表面附着颗粒或粉末物质,孔隙被填充,表面变得较为平坦。四种生物炭表面分布的-OH、-C=O、-C-O,以及花生壳生物炭与玉米秆生物炭表面的-CH_3、-CH_2、-O-参与了吸附;Langmuir方程可以较好地拟合四种生物炭对NH_4~+-N的等温吸附;吸附均在50 min内达到平衡,伪二级动力学方程均可以较好地描述生物炭对NH_4~+-N的动力学吸附过程;在溶液pH=7.00条件下,初始浓度为800 mg·L~(-1)的体系中,四种生物炭对NH_4~+-N的最大吸附量为9.5~15 mg·g~(-1),吸附能力大小为花生壳生物炭玉米秆生物炭竹屑生物炭杨木屑生物炭。研究表明,生物炭表面含氧官能团对吸附NH_4~+-N起到决定性作用,吸附为单分子层吸附,且由快速反应所控制,四种生物炭中吸附性最好的是花生壳生物炭。     

基于微观特性分析风积沙粉体掺入提高混凝土的抗冻性

为研究冻融-盐浸环境下风积沙粉体混凝土的微观特性,设计了强度等级为C35、C25的风积沙粉体混凝土,在浓度为0%、3%、6%硫酸镁溶液中采用快冻法进行抗冻性试验,同时借助核磁共振技术、场发射扫描电镜及能谱分析研究其孔隙特征、微观形貌及水化产物。结果表明,风积沙粉体的掺入显著提高混凝土的抗冻性,且适当提高强度等级,有利于提高风积沙粉体混凝土抗冻性,其中强度等级为C35的风积沙粉体混凝土在6%MgSO_4溶液中可承受高达425次冻融循环;相对于基准组,风积沙粉体混凝土中有发育状况良好的针柱状产物钙矾石、纤维状产物石膏生成,填充因冻胀应力作用产生的裂隙,使其内部有害及多害孔数量低于普通混凝土29.78%,抗冻性增强。     

Plant Availability of Sulfur Added to Finished Fertilizers

As single superphosphate availability decreases due to closure of aging manufacturing plants increasing attention is being paid to alternative phosphorus (P) and sulfur (S) sources. This glasshouse study, conducted under non-leaching conditions was undertaken to evaluate the S supplying capacity of gypsum, S bentonite, elemental S (ES) and a range of P containing fertilizers and those where ES was added as a coating or incorporated. The magnitude of crop response in terms of shoot biomass to applied S fertilizer sources followed the order of sulfates > powdered ES > coated/incorporated ES > S/bentonite. These results indicate that fertilizers containing a mixture of sulfate and micronized ES (<75 µm), either incorporated within the granule or coated onto the fertilizer are agronomically effective. The results also suggest that local S coating of finished fertilizers is a feasible alternative to S incorporation undertaken at a central fertilizer plant.     

阿维菌素等三种常规渔药对卡拉白鱼的急性毒性

采用半静态法,研究了三种常规渔药阿维菌素、三氯异氰脲酸和硫酸铜对卡拉白鱼(Chalcalburnus chal coides aralensis)急性毒性效应。结果表明:阿维菌素对卡拉白鱼24、48、72、96 h的半致死浓度分别为6.25、4.66、3.66和2.82 mg/L,安全浓度为0.77 mg/L;三氯异氰尿酸对卡拉白鱼24、48、72、96 h的半致死浓度分别为3.22、2.49、2.19、1.79 mg/L,安全浓度为0.45 mg/L;硫酸铜对卡拉白鱼24、48、72、96 h的半致死浓度分别为5.56、3.96、2.03、1.74 mg/L,安全浓度为0.6 mg/L。三种药物对卡拉白鱼毒性高低依次为:硫酸铜三氯异氯尿酸阿维菌素。三种常规渔药的安全浓度近于或高于生产中常用泼洒浓度,可放心使用。     

不同含水量天然硫酸盐盐渍土中二氧化碳和氧化亚氮的排放

Soil salinization may negatively affect microbial processes related to carbon dioxide(CO_2) and nitrous oxide(N_2O) emissions. A short-term laboratory incubation experiment was conducted to investigate the effects of soil electrical conductivity(EC) and moisture content on CO_2 and N_2O emissions from sulfate-based natural saline soils. Three separate 100-m long transects were established along the salinity gradient on a salt-affected agricultural field at Mooreton, North Dakota, USA. Surface soils were collected from four equally spaced sampling positions within each transect, at the depths of 0–15 and 15–30 cm. In the laboratory, artificial soil cores were formed combining soils from both the depths in each transect, and incubated at 60% and 90% water-filled pore space(WFPS) at 25?C. The measured depth-weighted EC of the saturated paste extract(EC_e) across the sampling positions ranged from 0.43 to 4.65 dS m~(-1). Potential nitrogen(N) mineralization rate and CO_2 emissions decreased with increasing soil EC_e, but the relative decline in soil CO_2 emissions with increasing ECe was smaller at 60% WFPS than at 90% WFPS. At 60% WFPS, soil N_2O emissions decreased from 133 μg N_2O-N kg~(-1) soil at EC_e 0.50 dS m~(-1) to 72 μg N_2O-N kg~(-1) soil at EC_e = 4.65 dS m~(-1). In contrast, at 90% WFPS,soil N_2O emissions increased from 262 μg N_2O-N kg~(-1) soil at EC_e = 0.81 dS m~(-1) to 849 μg N_2O-N kg~(-1) soil at EC_e = 4.65 dS m~(-1), suggesting that N_2O emissions were linked to both soil ECe and moisture content. Therefore, spatial variability in soil EC_e and pattern of rainfall over the season need to be considered when up-scaling N_2O and CO_2 emissions from field to landscape scales.