长白山典型林区森林资源利用适宜性分析

天然林保护不是简单的禁伐 .东北林区作为天然林保护的限伐林区 ,目前仍有一定数量的成过熟林采伐任务 ,如何科学合理地选择伐区非常重要 .鉴于传统森林资源采伐利用操作中存在顾此失彼的问题 ,现代科学的森林资源经营理论认为 ,森林资源利用要坚持可持续利用原则 ,并且要更多考虑森林资源的生态效益 .遥感 (RS)数据及地理信息系统 (GIS)技术 ,通过提供空间选择技术支撑 ,可以准确定位符合采伐标准的森林资源地理位置 ,并确定其面积、森林类型等信息 ,从而促进森林资源的科学合理利用 .本文综合考虑各方面要素 ,以长白山典型林区露水河林业局为例 ,以最大程度发挥森林生态系统的生态功能为原则 ,进行了森林资源利用状况评价 ,对研究区森林资源未来利用的空间选择以及采伐利用方式进行了探讨 ,以期为将来制订科学的森林经营策略提供依据 .

次生林经营基础研究进展

次生林是中国森林的主体 ,在结构组成、林木生长、生产力、林分环境等诸多方面与原始林和人工林有着显著的不同 .因此 ,经营好次生林对中国天然林保护等林业工程实施及国家生态安全建设具有重大意义 .本文在广泛收集国内外有关次生林研究结果的基础上 ,探讨了次生林经营领域中基础研究所涉内容 ,揭示出次生林经营研究中所关注的基础问题 ,提出了次生林经营基础研究的主要内容与方向 ,对今后次生林经营研究和中国天然林保护等林业工程建设具有参考价值 .

发展林业碳汇推动三北防护林体系建设

三北防护林体系建设作为中国六大林业重点工程之一,30年来取得了巨大成就。但长期以来,工程建设资金不足一直困扰着工程发展。林业碳汇的兴起和快速发展,将对其产生重大影响。本文在对林业碳汇进行分析的基础上,提出了加快发展林业碳汇推动三北防护林体系建设的建议。

近300年来中国森林的变迁

以清代以来史料为依据,在现代清查统计资料和前人研究成果的基础上,通过对森林变迁大体趋势及主要过程的客观把握,重新校订了1949年和1700年前人的估算数据,回溯估算了1750～1900年中国各省区每50年森林面积与森林覆被率值,并与现代森林清查资料衔接,分析1700～1998年近300年来中国森林变迁的时空特征。结果表明:近300年来中国现境内共减少森林面积约0.95×108ha,森林覆被率减少9.2个百分点,变化曲线呈先抑后仰;以1960s为界,此前呈加速递减态势,260年间减少森林面积达1.66×10

湖北省近500年区域干湿序列重建及其比较分析

在历史旱涝记载资料可靠性检验的基础上,重建了湖北省3个区域近500年来的干湿气候变化序列,并比较分析了各区域干湿气候变化的趋势特征、准周期性及跃变现象。结果表明:在3个区域中,鄂东区1570~1770、1890~1950年两个时段偏湿,1470~1520、1790~1830年则偏干;鄂北区偏湿时期主要在1470~1530、1710~1750、1850~1910年三个时段,1470~1530、1770~1830年则偏干;鄂西南区有1550~1610、1650~1710、1830~1890、1930~1990

Polyimides derived from 3,3 '-bis(N-aminophthalimide)

A novel diamine, 3,3'-bis(N-aminophthalimide) (BAPI), was prepared from 3,3'-bis(N-phenylphthalimide). Its structure was determined via IR, H-1 NMR, N-15 NMR, elemental analysis, and single-crystal X-ray diffraction analysis. A series of homo- and copolyimides were synthesized by a conventional one-step method in p-chlorophenol. The characteristic IR absorption bands of hydrazine-based imide groups were near 1780, 1750, 1350, 1100, and 730 cm(-1). The polymers showed good solubility in polar aprotic solvents and phenols at room temperature. The temperatures of 5% weight loss (T-5%) of the polyimides ranged from 495 to 530 degrees C in air. DMTA analyses indicated that the glass-transition temperatures (Tgs) of the polyimides were in the range 371-432 degrees C. These polymers had cutoff wavelengths between 350 and 400 nm. The polyimide films of 6FDA/BAPI and 4,4'-HQPDA/BAPI were colorless; other films were pale yellow or yellow.

Electrochemical behavior of redox species at carbon fibre microdisk array electrode modified with mixed-valent molybdenum(VI, V) oxide

In this study, electrode responses to a large number of electroactive species with different standard potentials at the molybdenum oxide-modified carbon fibre microdisk array (CFMA) electrode were investigated. The results demonstrated that the electrochemical behavior for those redox species with formal potentials more positive than similar to 0.0 V at the molybdenum oxide-modified CFMA electrode were affected by the range and direction of the potential scan, which were different from that at a bare CFMA electrode. If the lower limit of the potential scan was more positive than the reduction potential of the molybdenum oxide film, neither the oxidation nor the reduction peaks of the redox species tested could be observed. This indicates that electron transfer between the molybdenum oxide film on the electrode and the electroactive species in solution is blocked due to the existence of a high resistance between the film and electrolyte in these potential ranges. If the lower limit of the potential scan was more negative than the reduction potential of the molybdenum oxide film (similar to - 0.6 V), the oxidation peaks of these species occurred at the potentials near their formal potentials. In addition, the electrochemical behavior of these redox species at the molybdenum oxide-modified CFMA electrode showed a diffusionless electron transfer process. On the other hand, the redox species with formal potentials more negative than similar to - 0.2 V showed similar reversible voltammetric behaviors at both the molybdenum oxide-modified CFMA electrode and the bare electrode. This can be explained by the structure changes of the film before and after reduction of the film. In addition we also observed that the peak currents of some redox species at the modified electrode were much larger than those at a bare electrode under the same conditions, which has been explained by the interaction between these redox species and the reduction state of the molybdenum oxide film. (C) 2000 Elsevier Science Ltd. All rights reserved.

Chlorohydrin water swellable rubber compatibilized by an amphiphilic craft copolymer. I. Synthesis and characterization of compatibilizer PVA-g-PBA

The graft copolymerization of butyl acrylate onto poly(vinyl alcohol) with eerie ammonium nitrate as redox initiator in a aqueous medium has been investigated. The formation of graft copolymer was confirmed by means of IR, scanning electron microscopy (SEM), and wide-angle X-ray diffraction (WAXD). The percentage of mononer conversion and percentage of grafting varied with concentrations of initiator, nitric acid, monomer, macromolecular backbone (X-n = 1750, M = 80 000), reaction temperature and reaction time. Some inorganic salts and organic solvents have a great influence upon grafting. The reaction mechanism has been explored, and rate equations for the reaction are established. (C) 2000 John Wiley & Sons, Inc.

Cure processing modeling and cure cycle simulation of epoxy-terminated poly(phenylene ether ketone) .3. Determination of the time of pressure application

The curing temperature, pressure, and curing time have significant influence on finished thermosetting composite products. The time of pressure application is one of the most important processing parameters in the manufacture of a thermosetting composite. The determination of the time of pressure application relies on analysis of the viscosity variation of the polymer, associated with curing temperature and curing time. To determine it, the influence of the time of pressure application on the physical properties of epoxy-terminated poly(phenylene ether ketone) (E-PEK)-based continuous carbon fiber composite was studied. It was found that a stepwise temperature cure cycle is more suitable for manufacture of this composite. There are two viscosity valleys, in the case of the E-PEK system, associated with temperature during a stepwise cure cycle. The analysis on the effects of reinforcement fraction and defect content on the composite sheet quality indicates that the width-adjustable second viscosity valley provides a suitable pressing window. The viscosity, ranging from 400 to 1200 Pa . s at the second viscosity valley, is the optimal viscosity range for applying pressure to ensure appropriate resin flow during curing process, which enables one to get a finished composite with optimal fiber volume fraction and low void content. (C) 1997 John Wiley & Sons, Inc.

Study of ion solvation and ion association in polymer gel electrolyte with polyethylene oxide-co-polypropylene oxide as a plasticizer

Using a molal conductance method, ion solvation and ion association in polytriethylene glycol dimethacrylate (PTREGD)-LiClO4 gel electrolytes with amorphous ethylene oxide-co-propylene oxide (EO-co-PO, <(M)over bar (n)>, = 1750) as the plasticizer were investigated. It was found that the fraction of solute existing as single ions (alpha(i)) and ion pairs (alpha(p)) decreases, while that of triple ions (alpha(t)) increases linearly with increasing salt concentration. The dependence of these fractions on molecular weight of plasticizer was also examined. It was shown that alpha(i) and alpha(t) increase and alpha(p) decreases with increasing molecular weight. The result of temperature dependence of these fractions was very interesting: when the temperature is lower than 55 degrees C, alpha(i) increases while alpha(p) and alpha(t) decrease with increasing temperature; however, when the temperature is higher than 55 degrees C, the reverse is true.

Li_8SiN_4-Li_3N-BN体系中立方BN转化行为的研究

研究了高温高压下x·Li_8SiN_4-0.1(1-x)·Li_3N-0.9(1-x)·BN体系中立方氮化硼(cBN)的转化行为。Li_8SiN_4的存在可显著改善cBN晶体的发育,提高晶体质量。在4.2～5.5GPa,1340～1750℃范围内确定了x=4.8％时体系的cBN转化区,并对转化区内cBN转化率、平均生长速度、成核速度及破碎强度与转化温度和压力的关系进行了研究。

Crystallization of Clinopyroxene NaAlSi2O6 from Glass

Clinopyroxene NaAlSi2O6 was synthesized under varying pressures of 3.0-5.0GPa and at the temperature range of 1150.1750 degrees C, for periods of 1.480min. The glass material was completely transformed into homogeneous penetrating fibrous texture of clino

稀土（Nd，Pr）（Ⅲ）双酞菁衍生物的合成、表征和气敏特性

合成了八－４－（四氢糠氧基）酞菁钕（Ⅲ）（Ａ）、八－４－（β－萘氧基）酞菁钕（Ⅲ）（Ｂ）、八－４－（２，４－二叔戊基苯氧基）酞菁钕（Ⅲ）（Ｃ）和八－４－（２，４－二叔戊基苯氧基）酞菁镨（Ⅲ）（Ｄ）４种新的稀土（Ｎｄ、Ｐｒ）（Ⅲ）双酞菁衍生物，经元素分析、红外光谱、核磁共振谱表征．紫外可见光谱表明，它们在氯仿（１０￣（－６）ｍｏｌ／Ｌ）溶液中以单分子形式存在．热重分析证明配合物的热稳定性：Ｂ＞Ｃ～Ｄ＞Ａ．４种配合物成膜性好，Ｚ型沉积形成的单层ＬＢ膜材料对氨气有响应，特别是八－４－（四氢糠氧基）酞菁钕（Ⅲ）的膜材料对氨气很敏感，可与铜酞菁ＬＢ膜气敏性相比．

钠铝辉石由非晶态到晶态的转化研究

在3．0－5．0GPa，1150－1750℃，1－480min条件范围内，合成了钠铝辉石，通过XRD、SEM及IR分析对比研究了人工翡翠和天然翡翠的微观精细结构；通过DAT分析测定了人工翡翠与天然翡翠的熔点，淬火实验检验了人工翡翠的熔点，通过退火及老化实验研究了翡翠的热稳定性。同时还就人工翡翠和天然翡翠的硬度、密度及折射率等其它物化性质进行了比较研究。根据上述研究总结了合成优质钠铝辉石翡翠的最佳实验条件为压力＞4．0GPa，温度＞1450℃，晶化时间＞45min。